Huskey et al v. Ethicon, Inc. et al
Filing
272
MEMORANDUM OPINION AND ORDER (Motions for Summary Judgment) for the reasons stated herein, granting in part and denying in part 161 MOTION by Ethicon, Inc., Johnson & Johnson for Partial Summary Judgment; denying 178 MOTION by Ethicon, Inc., John son & Johnson for Partial Summary Judgment Based on Preemption of Certain Claims; denying 187 MOTION by Ethicon, Inc., Johnson & Johnson for Partial Summary Judgment on Punitive Damages; granting 163 MOTION by Allen Huskey, Jo Huskey for Partial Summary Judgment on Defendant Ethicon Inc.'s Separate Defenses. Signed by Judge Joseph R. Goodwin on 7/8/2014. (cc: attys; any unrepresented party) (skh)
IN THE UNITED STATES DISTRICT COURT
FOR THE SOUTHERN DISTRICT OF WEST VIRGINIA
CHARLESTON DIVISION
JO HUSKEY, et al.,
Plaintiffs,
v.
CIVIL ACTION NO. 2:12-cv-05201
ETHICON, INC., et al.,
Defendants.
MEMORANDUM OPINION AND ORDER
(Motions for Summary Judgment)
Pending before the court are the defendants’ Motion for Partial Summary Judgment
[Docket 161], Motion for Partial Summary Judgment Based on Preemption of Certain Claims
[Docket 178], Motion for Partial Summary Judgment on Punitive Damages [Docket 187], and
Plaintiffs Jo and Allen Huskey’s Motion for Partial Summary Judgment on Defendant Ethicon
Inc.’s Separate Defenses [Docket 163]. For the reasons stated below, the Motion for Partial
Summary Judgment [Docket 161] is GRANTED in part and DENIED in part, the Motion for
Partial Summary Judgment Based on Preemption of Certain Claims [Docket 178] is DENIED, the
Motion for Partial Summary Judgment on Punitive Damages [Docket 187] is DENIED, and
Plaintiffs Jo and Allen Huskey’s Motion for Partial Summary Judgment on Defendant Ethicon
Inc.’s Separate Defenses [Docket 163] is GRANTED.
I. Background
This case is one of more than 60,000 that have been assigned to me by the Judicial Panel on
Multidistrict Litigation in seven MDLs involving pelvic mesh products. Approximately 19,000 of
these cases reside in the In re Ethicon, Inc. MDL, MDL No. 2327.
The device at issue in this case is the Gynecare TVT Obturator (“TVT-O”), manufactured
by the defendants, Ethicon, Inc. and Johnson & Johnson, Inc. (collectively, “Ethicon”). The
TVT-O is a medical device that includes a mechanism used to place a mesh tape, or sling, under
the urethra to provide support to the urethra to treat stress urinary incontinence. (Mem. in Supp. of
Mot. for Partial Summ. J. [Docket 162], at 1).
Before being implanted with the TVT-O, Ms. Huskey suffered from stress urinary
incontinence which caused her to leak urine when she laughed, coughed, sneezed, exercised, or
experienced abdominal pressure. (See Byrkit Dep. [Docket 161-3], at 187:21-23; 189:3-6). Ms.
Huskey initially utilized pelvic floor strengthening exercises to alleviate her symptoms. (See
Huskey Dep. [Docket 161-4], at 308:18-309:4; 309:22-310:4). When those exercises failed to fully
remedy her stress urinary incontinence, she sought surgical treatment. (See id. at 312:22-313:1).
Ms. Huskey’s physician, Dr. Gretchen Byrkit, implanted the TVT-O device on February
23, 2011. (See Statement of Undisputed Facts Regarding Jo Huskey’s Medical History and
Condition [Docket 215], at 5). After the surgery, Ms. Huskey experienced several complications,
including erosion of the mesh and dyspareunia. (See id. at 5-6). Ms. Huskey underwent a revision
surgery with Dr. Sohail Siddique on November 18, 2011, which excised a portion of the TVT-O’s
mesh. (See id. at 6-7). After her revision, Ms. Huskey’s stress urinary incontinence symptoms
returned, and she experienced constant pelvic and vaginal pain. (See id. at 8).
2
Ms. Huskey and her husband, Allen Huskey, currently advance several claims against
Ethicon, including negligence, strict liability for design defect, strict liability for failure to warn,
strict liability for manufacturing defect, fraud, fraudulent concealment, constructive fraud,
negligent misrepresentation, negligent infliction of emotional distress, breach of express and
implied warranty, gross negligence, unjust enrichment, and violation of the Illinois Consumer
Fraud Act, 815 Ill. Comp. Stat. 505/1 et seq. (See Short Form Compl. [Docket 1], at 4-5).
II. Legal Standards
A. Summary Judgment
To obtain summary judgment, the moving party must show that there is no genuine issue as
to any material fact and that the moving party is entitled to judgment as a matter of law. Fed. R.
Civ. P. 56(a). In considering a motion for summary judgment, the court will not “weigh the
evidence and determine the truth of the matter.” Anderson v. Liberty Lobby, Inc., 477 U.S. 242,
249 (1986). Instead, the court will draw any permissible inference from the underlying facts in the
light most favorable to the nonmoving party. Matsushita Elec. Indus. Co. v. Zenith Radio Corp.,
475 U.S. 574, 587-88 (1986).
Although the court will view all underlying facts and inferences in the light most favorable
to the nonmoving party, the nonmoving party nonetheless must offer some “concrete evidence
from which a reasonable juror could return a verdict in his [or her] favor[.]” Anderson, 477 U.S. at
256. Summary judgment is appropriate when the nonmoving party has the burden of proof on an
essential element of his or her case and does not make, after adequate time for discovery, a
showing sufficient to establish that element. Celotex Corp. v. Catrett, 477 U.S. 317, 322-23
(1986). The nonmoving party must satisfy this burden of proof by offering more than a mere
“scintilla of evidence” in support of his or her position. Anderson, 477 U.S. at 252. Likewise,
3
conclusory allegations or unsupported speculation, without more, are insufficient to preclude the
granting of a summary judgment motion. See Felty v. Graves Humphreys Co., 818 F.2d 1126,
1128 (4th Cir. 1987); Ross v. Comm’ns Satellite Corp., 759 F.2d 355, 365 (4th Cir. 1985),
abrogated on other grounds, Price Waterhouse v. Hopkins, 490 U.S. 228 (1989).
B. Preemption
Federal preemption originates from the Constitution’s Supremacy Clause. See U.S. Const.
art. VI, cl. 2. 1 In addressing a preemption issue, the court’s first task is to determine whether
Congress intended to preempt. See Cal. Fed. Savings & Loan Ass’n v. Guerra, 479 U.S. 272,
280-81 (1978). Intent to preempt can manifest itself in three forms: field preemption, express
preemption, and conflict preemption. See H&R Block E. Enters. v. Raskin, 591 F.3d 718, 722 (4th
Cir. 2010). Field preemption occurs when the “federal scheme of regulation of a defined field is so
pervasive that Congress must have intended to leave no room for the states to supplement it[.]”
City of Charleston, S.C. v. A Fisherman’s Best, Inc., 310 F.3d 155, 169 (4th Cir. 2002). Express
preemption arises when “Congress expressly declares its intent to preempt state law.” Pinney v.
Nokia, Inc., 402 F.3d 430, 453 (4th Cir. 2005). Finally, conflict preemption occurs when “state law
stands as an obstacle to the accomplishment and execution of the full purposes and objectives of
Congress.” Hillsborough Cnty., Fla. v. Automated Med. Labs., Inc., 471 U.S. 707, 713 (1985)
(internal quotation omitted). Conflict preemption can also arise when “compliance with both
federal and state regulations is a physical impossibility[.]” Id. (internal quotation omitted).
Once Congress’s intent to preempt is determined, the focus turns to the scope of that
preemption. See Duvall v. Bristol-Myers-Squibb Co., 103 F.3d 324, 328 (4th Cir. 1996). Two
1
“This Constitution, and the Laws of the United States which shall be made in Pursuance thereof . . . shall be the
supreme Law of the Land . . . any Thing in the Constitution or Laws of any State to the Contrary notwithstanding.”
U.S. Const. art. VI, cl. 2.
4
presumptions guide this inquiry. See id. First, “‘the purpose of Congress is the ultimate
touchstone’ in every pre-emption case.” Medtronic, Inc. v. Lohr, 518 U.S. 470, 485 (1996)
(quoting Retail Clerks v. Schermerhorn, 375 U.S. 96, 103 (1963)). Second, a court starts “with the
basic assumption that Congress did not intend to displace state law.” Maryland v. Louisiana, 451
U.S. 725, 746 (1981). “This presumption is strongest when Congress legislates ‘in a field which
the States have traditionally occupied.’” S. Blasting Servs., Inc. v. Wilkes Cnty., N.C., 288 F.3d
584, 590 (4th Cir. 2002) (quoting Lohr, 518 U.S. at 485).
C. Choice of Law
The parties agree that Illinois’s choice-of-law rules apply in this case. Illinois has adopted
the most-significant-relationship test as enumerated in Restatement (Second) of Conflict of Laws.
See Townsend v. Sears, Roebuck & Co., 879 N.E.2d 893, 901 (Ill. 2007); Gregory v. Beazer E.,
892 N.E.2d 563, 578 (Ill. Ct. App. 2008). Under that test, courts should consider the following
factors: (1) the place where the injury occurred, (2) the place where the conduct causing the injury
occurred, (3) the domicile, residence, nationality, place of incorporation and business of the
parties, and (4) the place where the relationship, if any, between the parties is centered. See
Townsend, 879 N.E.2d at 901 (citing Restatement (Second) of Conflict of Laws § 145(2), at 414
(1971)). This choice of law analysis applies to each individual issue in a case. See Townsend, 879
N.E.2d at 901; Gregory, 892 N.E.2d at 578. Here, the surgery to implant the device and any
alleged injuries to the plaintiffs occurred in Illinois. Therefore, for the plaintiffs’ substantive
claims, I apply the law of Illinois.
The analysis is different for punitive damages. Illinois courts permit dépeçage, or a
separate choice-of-law analysis for each individual issue. See Townsend, 879 N.E.2d at 901-02
(explaining that Illinois follows the Restatement, which uses dépeçage). Ethicon urges the court to
5
apply New Jersey law to the punitive damages claim because the alleged conduct that gives rise to
the punitive damages claim occurred there. Ethicon’s argument is in line with the Restatement,
which states that “when the primary purpose of the tort rule involved is to deter or punish
misconduct, the place where the conduct occurred has peculiar significance.” Restatement
(Second) of Conflict of Laws § 145 cmt. e. The plaintiffs, appearing to agree with Ethicon,
likewise brief punitive damages in relation to New Jersey law. The focus of the punitive damages
inquiry is Ethicon’s corporate conduct, and that conduct allegedly occurred in New Jersey.
Therefore, New Jersey law applies to the plaintiffs’ punitive damages claim.
III. Failure to Warn
Ethicon first challenges the plaintiffs’ failure-to-warn claim. To recover on a
failure-to-warn claim, a plaintiff must establish that inadequate warnings rendered a product
unreasonably dangerous and caused the plaintiff’s injuries. Mikolajczyk v. Ford Motor Co., 901
N.E.2d 329, 345 (Ill. 2008). In the case of medical devices, the duty to warn is to the prescribing
physician, not the patient. Giles v. Wyeth, Inc., 500 F. Supp. 2d 1063, 1065 (S.D. Ill. 2007);
Hansen v. Baxter Healthcare Corp., 764 N.E.2d 35, 42 (Ill. 2002). Ethicon advances two
arguments against the plaintiffs’ failure-to-warn claim: (1) that the TVT-O’s warnings were
adequate because Dr. Byrkit was aware of the TVT-O risks, and (2) that the plaintiffs failed to
present evidence that the allegedly inadequate warnings caused the plaintiffs’ injuries. Ethicon’s
arguments fail on both counts.
A. Adequacy of Warnings
Ethicon contends that the TVT-O’s warnings were adequate because the implanting
physician, Dr. Byrkit, was independently aware of the TVT-O’s potential complications and risks.
In Illinois, “there is no duty to warn of a risk that is already known by those to be warned.” Proctor
6
v. Davis, 682 N.E.2d 1203, 1211 (Ill. App. Ct. 1997); see also Hansen, 764 N.E.2d at 42 (“[A]
prescription medical device manufacturer need not provide a warning of risks already known to
the medical community.”). A duty to warn arises only when there is “unequal knowledge and the
defendant, possessed of such knowledge, knows or should know that harm might occur if no
warning is given.” Proctor, 682 N.E.2d at 1211 (quotation marks omitted).
The plaintiffs argue that there is a dispute of fact as to whether the TVT-O’s warnings were
adequate because Dr. Byrkit was not warned about the TVT-O’s alleged potential to rope and curl
after implantation, polypropylene mesh’s propensity to degrade in vivo, or the risks associated
with small pore, heavy-weight mesh. Ethicon attempts to construe these risks as “mechanisms and
design defects” about which there is no duty to warn. (See Reply in Supp. of Mot. for Partial
Summ. J. [Docket 228], at 10). Ethicon cites no support for this proposition, and Illinois law
appears to make no such formalistic distinction. Illinois law requires that manufacturers warn of
“dangerous condition[s],” not merely the potential injuries that might result from use of the
product. Happel v. Wal-Mart Stores, Inc., 766 N.E.2d 1118, 1123 (Ill. 2002); Kennedy v.
Medtronic, Inc., 851 N.E.2d 778, 783 (Ill. App. Ct. 2006); see also Hansen, 764 N.E.2d at 42
(“dangerous propensities”). For instance, in Hansen, the Illinois Supreme Court found a dispute of
fact over the adequacy of warnings where a medical device manufacturer allegedly failed to warn
about the proper use of the device’s mechanisms. The defendant manufactured IV tubes and failed
to warn about the need to use particular tubes—those with threaded connections—with IVs
inserted into patients’ jugular veins. See Hansen, 764 N.E.2d at 43.
Here, the TVT-O’s potential to rope and fray, polypropylene’s propensity to degrade, and
complications associated with small pore mesh are all potential dangerous conditions about the
7
TVT-O of which Dr. Byrkit allegedly was not warned. Therefore, there is a dispute of fact about
whether the TVT-O’s warnings were adequate.
B. Causation
Ethicon also argues that the plaintiffs have failed to present evidence that the allegedly
inadequate warnings caused the plaintiffs’ harm. Ethicon argues that Dr. Byrkit did not rely on the
product’s IFU and that Dr. Byrkit would not have changed her decision to prescribe the device if
she had received a better warning.
In Illinois, causation under a products liability theory is the same as under a negligence
theory. See Smith v. Eli Lilly & Co., 560 N.E.2d 324, 328 (Ill. 1990). Therefore, a plaintiff must
prove that the defendant’s conduct was both the cause-in-fact and the legal cause of her injuries.
See Rodriguez v. Glock, Inc., 28 F. Supp. 2d 1064, 1070 (N.D. Ill. 1998). Illinois courts have
utilized two tests to determine whether a defendant’s conduct was a cause-in-fact: the “substantial
factor” test and the “but-for” test. Rodriguez, 28 F. Supp. 2d at 1070; Kerns v. Engelke, 369 N.E.2d
1284, 1292 (Ill. App. Ct. 1977), aff’d in part, 390 N.E.2d 859 (Ill. 1979). The “substantial factor”
test asks whether the defendant’s conduct is a “material element” and a “substantial factor” in
bringing about the plaintiff’s injury. Wehmeier v. UNR Indus., Inc., 572 N.E.2d 320, 335 (Ill. App.
Ct. 1991). Under the “but-for” test, “the defendant’s conduct is not a cause of an event if the event
would have occurred without it.” Kerns, 369 N.E.2d at 1292.
First, Ethicon argues that the allegedly inadequate warnings did not cause the plaintiffs’
injuries because Dr. Byrkit did not rely on the TVT-O’s Instructions for Use (“IFU”) in making her
decision. But there is no such testimony in the record. Dr. Byrkit read the IFU before implanting
the TVT-O, although she could not “recall the last time” she reviewed it. (See Byrkit Dep. [Docket
213-1], at 31:15-18; 67:7-11; 206:2-9). Dr. Byrkit also stated that she uses “the same” implantation
8
procedure described in the IFU on every patient. (See id. at 90:3-15; 102:1-9). There is, therefore,
sufficient evidence that Dr. Byrkit relied on the IFU in prescribing the TVT-O. 2
Second, Ethicon argues that Dr. Byrkit would not have changed her decision to prescribe
the TVT-O if she had received a better warning. 3 Dr. Byrkit’s testimony is inconsistent. On the
one hand, she testified that she would have changed her decision had she received a better warning:
Q:
A:
If you had been told that it shouldn’t be implanted in women who are active,
actively exercising, fit women, if you had been told that it shouldn’t be
implanted in those women, would you still have implanted it in Jo Huskey?
I don’t think I would.
(Byrkit Dep. [Docket 161-3], at 96:2-7). However, when asked whether she would again prescribe
the TVT-O to a patient “with the same signs and symptoms” as the plaintiff, Dr. Byrkit responded
that she “would use the TVT-O again.” (Id. at 279:1-10). She also testified that she continues to
use the TVT-O in her practice today. (Id. at 58:10-20). This conflicting testimony demonstrates the
existence of a genuine dispute of fact over whether Dr. Byrkit would have prescribed the TVT-O to
Ms. Huskey had she received a better warning. Therefore, under either the “substantial factor” or
the “but-for” test, the plaintiffs have set forth evidence creating a genuine dispute of fact on the
issue of causation.
2
Contrary to Ethicon’s suggestion, this case is readily distinguishable from Lewis v. Johnson & Johnson on this issue.
In Lewis, I dismissed the failure-to-warn claim in part because the treating physician affirmatively testified that she did
not rely on the IFU when prescribing the device. She also testified that she relied on a number of other factors,
including Ms. Lewis’s “symptoms, her voiding diary, her urodynamics, and physical exam.” In re Ethicon, Inc., Pelvic
Repair Sys. Products Liab. Litig., No. 2:12-cv-2327, 2014 WL 186869, at *4 (S.D. W. Va. Jan. 15, 2014). In this case,
however, there is no such testimony by Dr. Byrkit.
3
The parties disagree whether the plaintiffs are required to prove that Dr. Byrkit would have acted differently if she
received a better warning. The cases cited by the parties conflict on this issue. Compare Fisher v. Bristol-Myers
Squibb Co., 181 F.R.D. 365, 370 (N.D. Ill. 1998) (“[S]tep two of the causation battle will require [the plaintiff] to
show that his physician would not have prescribed Stadol if the defendants had provided adequate warnings.”), with
Noyola v. Johnson & Johnson, 85 C 2184, 1986 WL 14657, at *4 (N.D. Ill. Dec. 16, 1986) (“What a physician might
or might not have done had he been adequately warned is not an element plaintiff must prove as a part of her case.”). I
need not resolve this issue here because the plaintiffs presented evidence demonstrating that Dr. Byrkit would have
acted differently.
9
Accordingly, Ethicon’s motion for summary judgment on the failure-to-warn claim is
DENIED.
IV. Fraud-Based Claims and Warranty Claims
The plaintiffs bring several claims based on fraud: common law fraud, fraudulent
concealment, constructive fraud, and negligent misrepresentation. I refer to these claims as the
plaintiffs’ “fraud-based claims.” The plaintiffs also bring claims for breach of express and implied
warranties. Ethicon argues that all of these claims are simply repackaged failure-to-warn claims, to
which the learned intermediary doctrine applies and prevents recovery. I agree with Ethicon.
Under the learned intermediary doctrine, manufacturers of drugs and medical devices have
a duty to warn prescribing physicians, not end-users, about the product’s dangerous propensities.
Hansen, 764 N.E.2d at 42; Kirk v. Michael Reese Hosp. & Med. Ctr., 513 N.E.2d 387, 393 (Ill.
1987). The prescribing physician functions as a learned intermediary between the manufacturer
and the patient by deciding which product “best fits the patient’s needs and choos[ing] which facts
from the various warnings should be conveyed to the patient[.]” Kirk, 513 N.E.2d at 393. Ethicon
argues that because Illinois’s learned intermediary doctrine does not require medical device
manufacturers to warn end-users, the doctrine should bar the fraud-based claims premised on
representations made to Ms. Huskey. Otherwise, Ethicon contends, plaintiffs could simply plead
around the learned intermediary doctrine by characterizing failure-to-warn claims as fraud claims.
Illinois courts have not directly addressed this issue. However, courts around the country
have extended the learned intermediary doctrine to all claims based on a manufacturer’s failure to
warn, including claims for fraud, misrepresentation, and breach of warranty. See, e.g., Talley v.
Danek Med., Inc., 179 F.3d 154, 163-64 (4th Cir. 1999) (barring breach of warranty and fraud
claims); Lee v. Mylan, Inc., 806 F. Supp. 2d 1320, 1325 (M.D. Ga. 2011) (negligent
10
misrepresentation and breach of warranty claims); Beale v. Biomet, Inc., 492 F. Supp. 2d 1360,
1372 (S.D. Fla. 2007) (negligent misrepresentation); Southern v. Pfizer, Inc., 471 F. Supp. 2d
1207, 1218 (N.D. Ala. 2006) (fraudulent misrepresentation); In re Norplant Contraceptive Prods.
Liab. Litig., 955 F. Supp. 700, 709 (E.D. Tex. 1997) (misrepresentation and implied warranty);
Centocor, Inc. v. Hamilton, 372 S.W.3d 140, 169 (Tex. 2012) (fraud by omission).
Here, the plaintiffs’ fraud-based claims and warranty claims are simply repackaged
failure-to-warn claims. The plaintiffs appear to concede that their fraud-based claims are based
solely on representations made by Ethicon to Ms. Huskey. They state that these claims “in no way
rely on anything that Ethicon communicated to Dr. Byrkit, or anything that Dr. Byrkit told to Mrs.
Huskey,” (Pls.’ Mem. in Opp. to Ethicon’s Mot. for Summ. J. [Docket 213], at 15). But Ms.
Huskey was unable to identify any particular statements by Ethicon upon which she relied:
Q:
What information did you rely on that you received from Johnson &
Johnson and Ethicon to inform your decision about whether or not to have
the mesh surgery? You personally, not your doctor.
A:
There was no information as far as I’m aware of. It was not provided.
Q:
So what information from Johnson & Johnson and Ethicon about possible
risks and benefits associated with mesh or with the TVT mesh product did
you rely upon in making your decision to have the surgery?
A:
Once again, there was no information available on what I looked at.
Q:
There was no information available on what? On risks and benefits?
A:
Well, when I opened the brochure I looked through it, and what I saw and
then having the discussion with Dr. Byrkit, after what she had explained to
me and reading through the information that I did see, there wasn’t any big
warnings as far as, you know, if you look at a brochure and you look at
cautionary measures, normally they stand out on a brochure because that’s
one of the things where they want you to make sure you read that. And there
was nothing in that brochure that jumped out for, okay, there’s a FDA
warning, there was nothing that drew my attention to it as being something
highlighted as risks involved with mesh.
11
(Huskey Dep. [Docket 161-4], at 474:20-476:3). This inability to identify any particular fraudulent
statements upon which Ms. Huskey relied indicates that the gravamen of these claims is Ethicon’s
failure to warn Ms. Huskey about particular risks or dangers associated with the TVT-O. If the
learned intermediary doctrine “could be avoided by casting what is essentially a failure to warn
claim under a different cause of action . . . then the doctrine would be rendered meaningless.” In re
Norplant Contraceptive Products Liab. Litig., 955 F. Supp. 700, 709 (E.D. Tex. 1997).
Accordingly, I predict with confidence that, if confronted with this issue, the Illinois Supreme
Court would hold that the learned intermediary doctrine applies to all claims based on a medical
device manufacturer’s failure to warn, including fraud, fraudulent concealment, constructive
fraud, negligent misrepresentation, and breach of warranty. 4 Therefore, Ethicon’s motion for
summary judgment on fraud-based claims and warranty claims is GRANTED.
V. Unjust Enrichment, Manufacturing Defect Claims, Illinois Consumer Fraud Act
Ethicon moves for summary judgment on the plaintiffs’ claims for unjust enrichment,
manufacturing defect, and violation of the Illinois Consumer Fraud Act, 815 Ill. Comp. Stat. 505/1
et seq. The plaintiffs do not oppose summary judgment and withdraw these claims. (See Pls.’
Mem. in Opp. to Def. Ethicon’s Mot. for Partial Summ. J. [Docket 213], at 15, 20). Therefore,
Ethicon’s motion for summary judgment on claims for unjust enrichment, manufacturing defect,
and violation of the Illinois Consumer Fraud Act, 815 Ill. Comp. Stat. 505/1 et seq., is GRANTED
as unopposed.
4
I note that Ethicon did not expressly argue in its opening brief that the learned intermediary doctrine applies to the
warranty claims. “[T]he ordinary rule in federal courts is that an argument raised for the first time in a reply brief or
memorandum will not be considered.” Mew Sporting Goods, LLC v. Johansen, --- F. Supp. 2d ---, No. 1:13-cv-10,
2014 WL 222114, at *3 n.2 (N.D. W. Va. Jan. 21, 2014). However, Ethicon did assert that “[r]egardless of how [the
plaintiffs’ claims] are denominated, such claims can only succeed if the manufacturer gave defective warnings to the
learned intermediary.” (Mem. in Supp. of Mot. for Partial Summ. J. [Docket 162], at 13). This argument clearly
applies with equal force to the warranty claims, allowing me to consider it here.
12
VI. Punitive Damages
Ethicon moves for summary judgment on the issue of punitive damages [Docket 187]. As
previously stated, the law of New Jersey applies to the plaintiffs’ claim for punitive damages.
Ethicon argues that the New Jersey Product Liability Act (“NJPLA”), N.J. Stat. Ann. § 2A:58C-1
et seq., precludes an award of punitive damages in this case. The NJPLA provides that
manufacturers of medical devices are immune from punitive damages awards where their products
have been approved, licensed, or generally recognized as safe and effective by the FDA. The
relevant statute reads, in pertinent part,
Punitive damages shall not be awarded if a drug or device or food or food additive
which caused the claimant’s harm was subject to premarket approval or licensure
by the federal Food and Drug Administration under the “Federal Food, Drug, and
Cosmetic Act,” 52 Stat. 1040, 21 U.S.C. § 301 et seq. or the “Public Health Service
Act,” 58 Stat. 682, 42 U.S.C. § 201 et seq. and was approved or licensed; or is
generally recognized as safe and effective pursuant to conditions established by the
federal Food and Drug Administration and applicable regulations, including
packaging and labeling regulations. . . . For purposes of this subsection, the terms
“drug”, “device”, “food”, and “food additive” have the meanings defined in the
“Federal Food, Drug, and Cosmetic Act.”
N.J. Stat. Ann. § 2A:58C-5 (emphasis added). 5 Ethicon contends that the FDA has endorsed and
recognized the safety and effectiveness of the TVT-O in its 510(k) clearance. I decided this exact
issue in relation to Lewis v. Johnson & Johnson. See In re Ethicon, Inc., Pelvic Repair Sys. Prods.
Liab. Litig., No. 2:12-cv-4301, 2014 WL 186869, at *10 (S.D. W. Va. Jan. 15, 2014). As I
explained there, and in a separate opinion in that case, Lewis v. Johnson & Johnson, --- F. Supp. 2d
---, No. 2:12-cv-04301, 2014 WL 152374, at *4-6 (S.D. W. Va. Jan. 15, 2014), the FDA has not
“approved or licensed” or “generally recognized” the TVT-O as “safe and effective.” N.J. Stat.
Ann. § 2A:58C-5.
5
A portion of this statute, which I have omitted and which is not applicable here, was stricken by a New Jersey
appellate court as preempted by federal law. See McDarby v. Merck & Co., 949 A.2d 223 (N.J. Super. Ct. App. Div.
2008).
13
Ethicon states, without explanation, that this case is distinguishable from my holding in
Lewis. (Mem. in Supp. of Mot. for Partial Summ. J. on Punitive Damages [Docket 188], at 11).
Ethicon simply rehashes old arguments and, yet again, essentially asks that I reconsider an earlier
decision. As Ethicon is well aware, it is improper to ask the court “to rethink what the Court ha[s]
already thought through—rightly or wrongly.” In re C. R. Bard, Inc., 948 F. Supp. 2d 589, 649
(S.D. W. Va. 2013) (quotations omitted). Therefore, Ethicon’s motion for summary judgment on
the issue of punitive damages [Docket 187] is DENIED.
VII. Preemption
Ethicon moves for partial summary judgment based on preemption [Docket 178]. Ethicon
argues that the plaintiffs’ claims should be preempted to the extent that any claim contends “that
PROLENE* in mesh degrades and that degradation leads to other consequences, such as
infection.” (Mot. for Partial Summ. J. Based on Preemption of Certain Claims (“Preemption
Mot.”) [Docket 178], at 2). Ethicon bases this argument on the fact that the Prolene suture, which
they argue is a component part of the TVT-O, went through the FDA’s rigorous premarket
approval process, rather than the less stringent 510(k) clearance process. The Prolene suture is a
different medical device and, like the mesh contained in the TVT-O, is made of polypropylene.
This court examined that exact issue in Lewis v. Johnson & Johnson and found that the plaintiffs’
claims were not preempted. See --- F. Supp. 2d ---, No. 2:12-cv-04301, 2014 U.S. Dist. LEXIS
4985, at *32 (S.D. W. Va. Jan. 15, 2014); see also id. at *4-5 for a discussion of the differences
between 510(k) clearance and premarket approval. As noted in Lewis, the Supreme Court has
determined that claims related to devices approved through the FDA’s premarket approval process
are preempted while claims related to medical devices cleared through the FDA’s 510(k) clearance
14
process are not. See id. at *18-19; Riegel v. Medtronic, Inc., 552 U.S. 312, 322-23 (2008);
Medtronic, Inc. v. Lohr, 518 U.S. 470, 501-02 (1996).
Ethicon attempts to distinguish the instant case from Lewis and argues that the court has not
yet addressed the following issues:
(1) the fact that the FDA-approval of PROLENE* polypropylene for use in the
body is the “status quo” for that material and, whatever the Court’s views of the
safety and efficacy considerations of the 510(k) process, the approval of that
component is not stripped away because the device as a whole was later cleared
through the 510(k) process; (2) that Plaintiffs’ claims regarding degradation and
resulting inflammation and infection stem from the PROLENE*
polypropylene-based filaments, not the other parts of the kit; and (3) evidence that
the quantity of PROLENE* used does not have any effect on whether the
PROLENE* degrades when placed in the human body.
(Preemption Mot. [Docket 178], at 1-2). Ethicon’s arguments are without merit. As I explained in
Lewis,
Ethicon’s argument ignores the fact that the Prolene suture and the TVT are two
entirely different medical devices that went through different FDA processes.
Although Ethicon represents that the products are primarily composed of the same
material, it does not automatically follow that the material is safe in both devices.
The Prolene suture is a nonabsorbable surgical suture; the TVT is a form of
transvaginal mesh. The Prolene suture consists of a single filament of
polypropylene; the TVT is a mesh woven from knitted Prolene filaments. The
average Prolene suture is a few inches long; the TVT measures one-half inches by
sixteen inches, and contains many times the amount of polypropylene material. The
Prolene suture is not intended to adhere to human tissue; the TVT is designed to
adhere to human tissue. The Prolene suture is designed to be easily pulled out of the
body; the TVT cannot be removed without invasive surgery. . . .
The FDA’s approval of the Prolene suture necessarily related to its use as a suture;
it did not categorically approve Prolene filament for use in medical devices. When
the FDA approved the Prolene suture, it stated that it had concluded the Prolene
suture was “safe and effective for use as recommended in the submitted labeling.”
The FDA did not examine whether that same material was safe when woven
together to create a transvaginal mesh product. Ethicon would like the court to
determine that because the FDA found polypropylene is safe to use as a suture, it is
automatically safe to use in transvaginal mesh. Although purportedly constructed
of the same material, it is a different product, used in a different manner, for a
different purpose. The plaintiffs have presented evidence demonstrating the
15
difference in risk profiles between the Prolene suture and TVT, and evidence that
the process of weaving the filaments creates different surface characteristics in the
mesh. If a specific type of metal were approved for use in a bone screw via the
premarket approval process, it would not follow that that same type of metal was
safe in all medical devices, no matter what their function in the human body. The
same is true for Prolene filament. It does not follow that the same Prolene filament
that is safe for use as a suture is automatically safe for use in transvaginal mesh.
2014 U.S. Dist. LEXIS 4985, at *24-25 (internal citations omitted).
Additionally,
“[p]ersuasive authority from other district courts . . . indicates that the preemption
analysis is not applied differently to the component parts of a medical device and
the medical device itself[.]” Gavin v. Medtronic, Inc., CIV.A. 12-0851, 2013 WL
3791612, at *11 (E.D. La. July 19, 2013). Interestingly, the shoe is normally on the
other foot—the defendant is arguing that a cause of action is preempted because a
device underwent premarket approval, while the plaintiff is arguing there is no
preemption because a component part of the device underwent 510(k) clearance.
Courts addressing this issue have determined that a device should not be broken
into its component parts in order to apply a preemption analysis . . . . The same
reasoning used in those cases is applicable here: analyzing the component parts of a
device separately from the device itself simply does not make sense.
“To require that a distinction be drawn between the approval process of the
individual components of a system and the system itself, would, it seems, add a
level of complication to the medical device approval process not anticipated by
Congress, the FDA, or medical device manufacturers.” Lewkut, 724 F. Supp. 2d at
656. “It makes no sense—indeed, it would probably be impossible—to pick apart
the components of a medical device and apply different preemption analyses to
different components.” Riley, 625 F. Supp. 2d at 780. Determining preemption
based upon the component parts of a device, rather than the device as a whole,
would create a legal quagmire whereby tort claims against one part of a device are
preempted while tort claims against another part of a device are not. Indeed, this is
exactly what Ethicon would like the court to declare—as Ethicon noted, its “motion
addresses only the use of PROLENE filaments and does not address other alleged
defects, such as mesh pore size.” (Defs.’ Mot. for Summ. J. [Docket 128], at 1).
Analyzing each component of a medical device separately to determine whether
claims are preempted would create a doctrine that forces courts to dissect every
medical device. In that world, a different preemption analysis would apply to each
part of the device, rather than the device as a whole. See Phillips, 2010 WL
2270683, at *5 n.4 (noting the “serious practical difficulties” with separating the
device from its component parts to determine preemption). Particularly in complex
litigation such as this, bright line rules are important to create clarity for all parties
16
involved. The doctrine Ethicon asks this court to accept would only serve to create
chaos in a field that is already difficult to navigate. Each involved party should be
able to determine whether tort claims regarding a medical device are preempted
based upon the review process the device actually went through. If the TVT had
gone through the premarket approval process while the polypropylene filament had
gone through the 510(k) process, I cannot imagine that Ethicon would think the
component parts of a device should be analyzed separately from the device itself.
As discussed above, Ethicon itself has recognized the importance of viewing the
TVT as a whole, rather than just its component parts. Just as “a device receiving
premarket approval cannot be separated into its component parts to avoid
application of express preemption,” Gross, 858 F. Supp. 2d at 487, a device
receiving 510(k) approval cannot be separated into its component parts to create
express preemption.
Id. at *27-32. None of Ethicon’s arguments demonstrate that I should deviate from this reasoning.
Although Ethicon may have rephrased some of its arguments and has submitted an additional
declaration from an Ethicon employee, the legal reasoning here is the same as in Lewis.
Ethicon also argues that I should reconsider my ruling in Lewis based on the reasoning in
two other cases: Bertini v. Smith & Nephew, Inc., No. 13 Civ. 79, 2014 U.S. Dist. LEXIS 35837
(E.D.N.Y. Mar. 17, 2014) and Simon v. Smith & Nephew, Inc., No. 13 CIV. 1909 PAE, 2013 WL
6244525 (S.D.N.Y. Dec. 3, 2013). These cases concern the same allegedly defective hip
replacement system, the R3 Acetabular System, developed by Smith & Nephew. See Bertini, 2014
U.S. Dist. LEXIS 35837, at *2; Simon, 2013 WL 6244525, at *4. The R3 System “is a hip implant
system used in total hip replacement procedures.” Bertini, 2014 U.S. Dist. LEXIS 35837, at *2.
“The R3 System is made up of the Acetabular Cup (shell) . . . and one of several possible liners.”
Id. The purpose of the liner is “to prevent the loosening of the hip components, which is a defect in
total hip replacement systems that often results in pain and a decrease in the hip implant’s
stability.” Id. The R3 System received 510(k) clearance from the FDA. Id. at *2-3. Later, Smith &
Nephew developed a new hip replacement system, the Birmingham Hip Resurfacing (“BHR”)
System. Id. at 3. The BHR System was approved through the premarket approval process. Id.
17
Thereafter, the FDA granted supplemental premarket approval to the BHR System using the R3
acetabular metal hip liner. Id. at 3-4. Essentially, the premarket approval of the BHR System was
amended to include one of the same components as the R3 System—the R3 acetabular metal hip
liner. See id. Importantly, in both Bertini and Simon, the plaintiff was implanted with an R3
System (which received 510(k) clearance rather than premarket approval), not the BHR System.
See Bertini, 2014 U.S. Dist. LEXIS 35837, at *12; Simon, 2013 WL 6244525, at *4.
In Simon, the plaintiff argued that the R3 System was defectively designed. See 2013 WL
6244525, at *4. The plaintiff argued that the design defect claims were not preempted because the
R3 system was not approved through the premarket approval process. See id. at *4. The defendant
argued that each of the plaintiff’s claims “challenge[d] the safety and effectiveness of the optional
metal liner; and the R3 metal liner was indeed [premarket]-approved.” (Id.). The court’s actual
holding in Simon was that the plaintiff’s Amended Complaint failed to state a claim for strict
liability, negligence, and breach of implied warranty. See id. at *6, 7, 8. However, the court also
found that even if the complaint had stated claims, those claims would have been preempted. See
id. In relevant part, the court stated:
[E]ven if the Amended Complaint were fairly read to assert a claim of design defect
based solely on the optional metal liner, any such claim would be preempted. That
is because the optional metal liner received supplemental [premarket] approval in
conjunction with the BHR System. As noted, design defect claims regarding a
[premarket]-approved device are squarely preempted by the [Medical Device
Amendments to the Food, Drug and Cosmetic Act]. Such preemption extends to a
component of a [premarket]-approved device.
Id. at *7. To support this proposition, the court cited to Lewkut v. Stryker Corp., 724 F. Supp. 2d
648, 656 (S.D. Tex. 2010), which stated: “To require that a distinction be drawn between the
approval process of the individual components of a system and the system itself, would, it seems,
add a level of complication to the medical device approval process not anticipated by Congress,
18
the FDA, or medical device manufacturers.” Id. It also cited to Riley v. Cordis Corp., 625 F. Supp.
2d 769, 780 (D. Minn. 2009), for the proposition that “separating components of
[premarket]-approved device to apply different preemption analysis ‘makes no sense.’” Id.
I respectfully disagree with the Simon court’s analysis. First, neither Lewkut nor Riley held
that premarket approval of a component part of a device meant that all claims against a 510(k)
cleared device were preempted. Notably, Lewkut dealt with a device that was, as a whole,
approved through the premarket approval process. See 724 F. Supp. 2d at 652. That device
contained a component that, prior to the device’s premarket approval, was cleared through the
510(k) process. See id. The court in Lewkut found the fact that the component part “was previously
approved through only the § 510(k) process, and was commercially available when” the medical
device received premarket approval did “not change the fact that it was later subject to the more
rigorous scrutiny of the [premarket approval] process as a component of” the full medical device.
Id. at 657. The court ultimately held that because the entire device had gone through the premarket
approval process, the plaintiff’s claims were preempted. See id. at 658. The Simon court’s reliance
on Lewkut is misplaced; in Lewkut, the entire device had received premarket approval.
The other case relied upon by the Simon court, Riley, also dealt with a device that had
received premarket approval. See 625 F. Supp. 2d at 774-75. The plaintiff there argued that
because the approved device was coated with a drug, the preemption analysis of Riegel v.
Medtronic, Inc., 552 U.S. 312, 322-23 (2008), should not apply. See id. at 779. The Riley court
noted that the device at issue was “not merely a drug or merely a drug-delivery system; it [was]
instead a compound of mechanical and chemical parts that work together as a single medical
device. In approving the [device], the FDA exercised its authority to regulate medical devices, not
its authority to regulate drugs.” Id. It also noted that the plaintiff’s claims were “manifestly claims
19
against the device as a whole.” Id. at 780. The court found that because the FDA had approved and
regulated the completed product as a medical device, the court should apply the express
preemption analysis set forth in Riegel. See id.
As the above discussion reveals, the Simon court’s reliance on Lewkut and Riley as support
for applying total preemption to a medical device that only received 510(k) clearance was
misguided. Both Lewkut and Riley dealt with whether product liability claims regarding a device
that received premarket approval were preempted; the Supreme Court has been clear that they are.
See Riegel, 552 U.S. at 330 (“State requirements are pre-empted under the [Medical Device
Amendments] . . . to the extent that they are ‘different from, or in addition to’ the requirements
imposed by federal law.”). The Supreme Court has been equally clear that product liability claims
regarding a device that received 510(k) clearance are not preempted. See Medtronic v. Lohr, 518
U.S. 470, 494 (1996). The courts in Lewkut and Riley followed the Supreme Court precedent that
claims against a device that receives premarket approval are generally preempted. 6 The court in
Simon, on the other hand, deviated from Supreme Court precedent which found that claims against
a device receiving 510(k) approval are not preempted. Read in their entirety, the cases cited in
Simon do not suggest that premarket approval of a component part of a device means that claims
against the entire device should be preempted.
The Bertini court’s analysis likewise seems to confuse the preemption analysis. The court
repeatedly notes that preemption applies to a device as a whole rather than component parts but
then finds that the plaintiffs’ claims are preempted because of the premarket approval of a
component part, ignoring the status of the device as a whole:
6
Claims against a device that received premarket approval are not preempted to the extent that they assert that the
device manufacturer failed to obey FDA requirements. See Riegel, 552 U.S. at 330 (stating that the Federal Food, Drug
and Cosmetic Act “does not prevent a State from providing a damages remedy for claims premised on a violation of
FDA regulations”). However, this exception is irrelevant to the instant case.
20
While the R3 metal liner is just one part of the hip replacement system, it is the
main focus of plaintiffs’ Complaint. Plaintiff[]s attribute Mr. Bertini’s injuries to
two separate but interrelated defects: “the loosening of the R3 metal liner and the
failure of the locking mechanism in the R3 System to hold the R3 metal liner in
place.” The liner’s purpose is to prevent the other hip components, including the R3
acetabular shell and its locking mechanism, from loosening. Similarly, the locking
mechanism feature is supposed to ensure that the liner stays connected to the R3
acetabular shell; essentially, it assists the liner in performing the liner’s function.
Although plaintiffs describe these device failures as two separate defects, they are
in large part describing the same phenomena—the R3 metal liner's inability to
attach to the R3 acetabular shell, which resulted in plaintiffs’ injuries.
Because plaintiff’s injuries are alleged to have been caused by the failure of
multiple components, I must apply a preemption analysis for the hip replacement
system as one unit, and not examine each individual component. Assuming that I
did apply a preemption analysis to each individual component, I would find that
plaintiff’s claims with respect to the R3 metal liner, which received PMA approval,
would be preempted, whereas the claims related to the R3 System, including the R3
acetabular shell and locking mechanism, would not be preempted. But, left solely
with their claims with respect to the R3 System, plaintiffs would be unable to show
that the R3 acetabular shell and its locking mechanism alone proximately caused
plaintiffs’ injuries, because plaintiffs have plead that the R3 System and the R3
metal liner together were the cause of plaintiff’s injuries. Plaintiffs would have to
prove that the R3 acetabular shell did not stay attached to the R3 metal liner,
without being able to argue, as they have repeatedly throughout this litigation, that
this failure to attach was due in large part to the R3 metal liner improperly
loosening from the R3 acetabular shell. Therefore, if a claim involving the R3 metal
liner’s alleged defect is preempted, the entire claim should be dismissed because
plaintiffs will be unable to sufficiently plead the remainder of that claim.
2014 U.S. Dist. LEXIS 35837, at *12-14. I disagree with this reasoning. In approving the BHR
system with the liner from the R3 System, the FDA did not examine the R3 liner’s safety and
efficacy with regard to other hip replacement systems—the FDA was instead looking at whether
the BHR System, as a whole, was safe and effective. It is difficult to understand why the Bertini
court found that premarket approval of one medical device meant that claims against an entirely
different medical device were preempted. While these cases from other district courts outside of
the Fourth Circuit may be cited to as persuasive authority, I do not find either of them persuasive in
light of existing Supreme Court precedent and federal regulations.
21
Preemption is based on FDA premarket approval of a medical device, not its component
parts. Supreme Court precedent speaks to whether a specific device underwent premarket approval
or 510(k) clearance. See generally Riegel, 552 U.S. 312; Lohr, 518 U.S. 470. The relevant federal
statute speaks to the approval or clearance of devices. See generally 21 U.S.C. § 360, et seq. The
regulations interpreting the preemption provision of that federal statute discuss devices. See 21
C.F.R. 808.1. As I stated in Lewis, “[j]ust as a device receiving premarket approval cannot be
separated into its component parts to avoid application of express preemption, a device receiving
510(k) approval cannot be separated into its component parts to create express preemption.” 2014
U.S. Dist. LEXIS 4985, at *32 (internal quotation omitted). The Supreme Court and federal
regulations instruct that state requirements are preempted “only when the Food and Drug
Administration has established specific counterpart regulations or there are other specific
requirements applicable to a particular device.” Riegel, 552 U.S. at 322 (quoting 21 C.F.R. §
808.1(d) (emphasis added). The fact that the Prolene suture underwent premarket approval is
irrelevant to whether the 510(k) process sets forth specific requirements applicable to the TVT-O.
The law is clear that it does not.
For the reasons set forth above, Ethicon’s motion for partial summary judgment based on
preemption [Docket 178] is DENIED.
VIII. Separate Defenses
The plaintiffs move for summary judgment on several of Ethicon’s separate defenses
[Docket 163]. Ethicon listed its separate defenses in its Master Answer and Jury Demand of
Defendant Ethicon, Inc. to First Amended Master Complaint [Docket 2-2]. In response to the
plaintiffs’ motion, Ethicon now withdraws most of these defenses. Accordingly, for the following
defenses, the plaintiffs’ motion for summary judgment is GRANTED as unopposed: 1, 3, 4, 5, 6,
22
7, 8, 9, 11, 13, 14, 25, 30, 32, 33, 35, 42, 45, 49, 50, 51, 52, 55, 57, 58, 60, 62, 67, 68, 76, 77, 78,
and 79.
Ethicon opposes summary judgment on the remaining separate defenses, which relate to
punitive damages, preemption, and federal regulations. Ethicon refers the court to the arguments
contained in its Motion for Partial Summary Judgment on Punitive Damages [Docket 187] and
Motion for Partial Summary Judgment Based on Preemption of Certain Claims [Docket 178]. I
have already addressed and rejected Ethicon’s arguments contained in those motions and
supporting memoranda. Therefore, for the following defenses, which relate to punitive damages,
preemption, and federal regulations, the plaintiffs’ motion for summary judgment is GRANTED:
10, 15, 16, 17, 18, 19, 20, 22, 23, 24, 39, 59, 74, and 75.
IX. Conclusion
For the reasons stated above, Ethicon’s Motion for Partial Summary Judgment [Docket
161] is GRANTED in part and DENIED in part, Ethicon’s Motion for Partial Summary
Judgment Based on Preemption of Certain Claims [Docket 178] is DENIED, Ethicon’s Motion for
Partial Summary Judgment on Punitive Damages [Docket 187] is DENIED, and Plaintiffs Jo and
Allen Huskey’s Motion for Partial Summary Judgment on Defendant Ethicon Inc.’s Separate
Defenses [Docket 163] is GRANTED.
The court DIRECTS the Clerk to send a copy of this Order to counsel of record and any
unrepresented party.
23
ENTER:
24
July 8, 2014
Disclaimer: Justia Dockets & Filings provides public litigation records from the federal appellate and district courts. These filings and docket sheets should not be considered findings of fact or liability, nor do they necessarily reflect the view of Justia.
Why Is My Information Online?