Rachel Krumpelbeck v. Breg Inc., et al

Filing

OPINION: we AFFIRM the district court's grant of summary judgment as to Krumpelbeck's claims of nonconformance with representations, negligence, breach of express warranty, breach of implied warranty, negligent misrepresentation and fraud. We REVERSE and REMAND for further proceedings as to Krumpelbeck's statutory claims for defective design and inadequate warning or instruction, decision not for publication pursuant to local rule 206. Ralph B. Guy , Jr., Circuit Judge; Bernice Bouie Donald, AUTHORING Circuit Judge and John Corbett O'Meara, U.S. District Judge for the Eastern District of Michigan, sitting by designation.

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NOT RECOMMENDED FOR FULL-TEXT PUBLICATION
File Name: 12a0874n.06
No. 11-3726

FILED

UNITED STATES COURT OF APPEALS
FOR THE SIXTH CIRCUIT

Aug 10, 2012

RACHEL KRUMPELBECK,
Plaintiff-Appellant,
v.
BREG, INC., et al.,
Defendants-Appellees.

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LEONARD GREEN, Clerk

ON APPEAL FROM THE UNITED
STATES DISTRICT COURT FOR THE
SOUTHERN DISTRICT OF OHIO

Before: GUY and DONALD, Circuit Judges, and O’MEARA, District Judge.*

BERNICE BOUIE DONALD, Circuit Judge. This appeal arises from a product liability
action against medical device manufacturer Breg, Inc., for injuries allegedly resulting from Rachel
Krumpelbeck’s use of a Breg pain pump. Krumpelbeck’s complaint asserted seven claims against
Breg: (1) strict liability - design defect; (2) strict liability - warning defect; (3) strict liability nonconformance with representations; (4) negligence; (5) breach of express warranty; (6) breach of
implied warranty; and (7) negligent misrepresentation and fraud. Breg filed a motion for summary
judgment in which it argued that it was reasonably unaware of the risk of injury that Krumpelbeck
sustained, and therefore, that it had no duty to warn. Alternatively, Breg argued that Krumpelbeck
could not show that a failure to warn caused her injury. The district court granted Breg’s motion for

*

The Honorable John Corbett O’Meara, United States District Court for the Eastern District
of Michigan, sitting by designation.

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summary judgment and dismissed Krumpelbeck’s complaint. Krumpelbeck timely appealed. While
we find no error in the district court’s dismissal of Krumpelbeck’s common law claims and her
statutory claim of nonconformance with representations, we find that, construing the evidence in the
light most favorable to Krumpelbeck, there are genuine disputes of fact that could allow a reasonable
jury to find in her favor on her statutory claims of defective design and inadequate warning or
instruction. Accordingly, we AFFIRM in part, REVERSE in part, and REMAND for further
proceedings.
I. BACKGROUND
On March 3, 2005, Plaintiff-Appellant Rachel Krumpelbeck, then seventeen years old,
underwent arthroscopic surgery on her shoulder. Her surgeon, Dr. Paul Favorito, used a Breg pain
pump device to administer a local anesthetic to Krumpelbeck’s shoulder for four days following her
surgery. Dr. Favorito inserted the pain pump catheter directly into Krumpelbeck’s shoulder joint to
deliver the prescribed pain medication. In the months following her surgery, Krumpelbeck
experienced extreme pain, and worsening stiffness, clicking, and popping in her shoulder joint. In
December 2007, Krumpelbeck was diagnosed with glenohumeral chondrolysis, a painful condition
involving the permanent destruction of articular cartilage in the shoulder joint. According to her
doctor, Krumpelbeck’s prognosis is poor, and she will likely require several complete shoulder
replacements during her lifetime.
On February 6, 2009, Krumpelbeck filed a seven-count complaint against Breg, the
manufacturer of the pain pump; Orthofix International NV, Breg’s parent corporation; and Advanced

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Technology, a wholesale distributer of medical equipment, including the Breg pain pump.1 The
complaint alleged strict liability for defective design, inadequate warnings, and failure of the pump
to conform to representations. The complaint also asserted claims for negligence, breach of express
and implied warranty, negligent misrepresentation, and fraud.
On October 15, 2010, Breg filed a motion for summary judgment, arguing that at the time
of Krumpelbeck’s surgery neither Breg nor Krumpelbeck’s treating physician had knowledge of any
risk associated with the continuous intra-articular infusion of anesthetic and, in particular, any link
to chondrolysis. Breg also argued that all common law claims Krumpelbeck asserted were barred
by the April 2005 amendment to the Ohio Products Liability Act (“OPLA”), which expressly
abrogated all common law causes of action sounding in products liability. Krumpelbeck filed a
response under seal on November 5, 2010, arguing that there were disputed facts regarding the
foreseeability of harm that precluded summary judgment. On November 22, 2010, Breg filed a
reply.
On December 2, 2010, after the pleadings were fully ripe for review, Krumpelbeck filed as
a stand-alone docket entry the expert report of Dr. Suzanne Parisian, which was taken in a similar
pain-pump case pending in another district. On December 23, 2010, seven weeks after filing her
memorandum, Krumpelbeck filed an additional 2,827 pages of deposition transcripts, also as
independent docket entries, which included the deposition of Dr. Parisian.

1

Orthofix and Advanced Technology are no longer parties to the case.
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On December 27, 2010, the district court entered an order granting Breg’s motion for
summary judgment. Krumpelbeck v. Breg, Inc., 759 F. Supp. 2d 958 (S.D. Ohio 2010). The court
agreed that “[a]s of the time of Plaintiff’s surgery, the now-purported association between
chondrolysis and anesthetic infusion in the shoulder joint was unknown to Defendant, and, indeed,
to the entire scientific community,” and “[t]herefore, Defendant breached no duty, and the [pain
pump] was not defective for inadequate warnings or instructions.” Id. at 974. The court rejected
Krumpelbeck’s design defect claim for the same reason—because there was no evidence that Breg
knew or should have known of the risk, Krumpelbeck could not show that “the foreseeable risks
associated with [the product’s] design . . . exceeded the benefits.” Id. at 975. The district court
dismissed Krumpelbeck’s complaint in its entirety.
On January 17, 2011, Krumpelbeck filed a motion to alter and/or obtain relief from judgment.
In the motion, counsel posited that, for some reason “not known to Plaintiff,” the Court “overlooked”
Dr. Parisian’s testimony in granting Breg’s motion for summary judgment. Krumpelbeck argued that
Dr. Parisian’s report and deposition “directly state[] that there was ample medical literature and other
evidence in existence at the time of Plaintiff’s surgery that Breg knew or should have known of the
risk of harm from using pain pumps inside the joint space prior to March 2005.” Krumpelbeck urged
the district court to “now consider these documents and expert testimony as they are representative
of that which will be presented at the trial of this matter . . . and it directly addresses those omissions
in the record that led the Court to grant the Defendant’s motion for summary judgment.”
Krumpelbeck also argued for the first time that her common law claims were not pre-empted by the
OPLA because her injury occurred before the effective date of the April 2005 amendment.
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The district court denied Krumpelbeck’s motion,2 citing Southern District of Ohio Local Rule
7.2(d), which provides that “all evidence then available shall be discussed in, and submitted no later
than, the primary memorandum of the party relying upon such evidence.” (emphasis added). In
light of that rule, and given the fact that Dr. Parisian’s deposition and report were not “newly
discovered evidence,” the court stated that it would not consider Dr. Parisian’s report or deposition,
nor any of the other late-filed documents that Krumpelbeck submitted. The court pointed out that,
apart from being untimely, Krumpelbeck’s “supplementary exhibits” were filed without any
explanation as to how they supported her memorandum in opposition. The district court stated that
it could not “infer arguments from exhibits that are not referenced in the pleadings nor be expected
to analyze 27,000 [sic] pages of facts without any direction,” and chastised counsel for failing “to
synthesize those facts and present them to the Court in a comprehensive fashion.” The district court
made clear, however, that even if it were to consider these documents, they were insufficient on their
face to establish the existence of a triable issue.

2

Krumpelbeck’s motion sought relief pursuant to both Rule 59(e) and Rule 60(b) of the
Federal Rules of Civil Procedure. Rule 59(e) was amended effective December 1, 2009, to allow
parties twenty-eight days after entry of judgment to file a motion to alter or amend. The district
court, citing an older version of Rule 59(e), erroneously stated that Krumpelbeck’s motion to alter
or amend was untimely because it was filed more than ten days after the entry of judgment.
Therefore, the court only considered Krumpelbeck’s motion under the much higher standard required
for granting a Rule 60(b) motion for relief from judgment.
Although the district court undeniably erred in stating that Krumpelbeck’s Rule 59(e) motion
was untimely, Breg correctly notes that Krumpelbeck’s counsel has not presented this issue for
review in the present appeal, which makes assignments of error only with regard to the district
court’s summary judgment analysis. Accordingly, we limit our review to those issues. We note,
however, that Krumpelbeck is not prejudiced by this limitation, as her Rule 59(e) motion essentially
raised the same objections to the district court’s summary judgment analysis that Krumpelbeck now
raises on appeal.
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II. ANALYSIS
On appeal, Krumpelbeck argues that the district court applied the wrong version of the
OPLA, thereby erroneously determining that her common law claims were barred by the April 2005
amendments to the Act. Krumpelbeck also argues that the district court erred in dismissing without
discussion or analysis certain claims that were pleaded in her complaint but which Breg did not
address in its motion for summary judgment. Finally, Krumpelbeck maintains that summary
judgment was improper on her claims of defective design, defects due to inadequate warning or
instruction, and defects due to nonconformance with representations because she put forth sufficient
evidence from which a reasonable jury could find in her favor.
A. Standard of review
We review a district court’s order granting summary judgment de novo. Int’l Union v.
Cummins, Inc., 434 F.3d 478, 483 (6th Cir. 2006). A motion for summary judgment should be
granted if the evidence before the court shows that there is no dispute of material fact and that the
movant is entitled to judgment as a matter of law. Fed. R. Civ. P. 56(a); see Celotex Corp v. Catrett,
477 U.S. 317, 322 (1986). The moving party has the burden of showing the absence of genuine
disputes over facts which, under the substantive law governing the issue, might affect the outcome
of the action. Celotex, 477 U.S. at 323. The party opposing the motion may not rest upon the
allegations set forth in the pleadings; rather, it must show that there is some evidence, more than a
mere scintilla, establishing a genuine issue for trial. See Anderson v. Liberty Lobby, Inc., 477 U.S.
242, 248 (1986).
B. Applicable version of the OPLA
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The district court did not address the merits of Krumpelbeck’s argument that the preamendment version of the OPLA—the version in effect at the time of her March 2005
surgery—should govern this case rather than the post-amendment version in effect at the time her
cause of action arose. Because Krumpelbeck failed to timely raise this argument below, we find no
error in the district court’s dismissal of Krumpelbeck’s common law claims.
C. Notice of risk
The thrust of Breg’s motion for summary judgment, and the primary basis on which the
district court granted the motion, was that Breg was reasonably unaware of the risk of chondrolysis
at the time of Krumpelbeck’s surgery in March 2005 and, thus, had no duty to warn of this risk. On
appeal, Krumpelbeck argues that there is a genuine dispute of fact as to whether the information
available to the scientific community as of March 2005 was sufficient to put Breg on notice of the
risk of harm from the intra-articular use of its pain pumps. She also contends that the FDA’s
repeated refusal to clear Breg’s device for orthopedic and/or intra-articular use should have placed
Breg on notice of a risk of harm of the nature that Krumpelbeck suffered. Moreover, Krumpelbeck
points out that several of her claims do not have a notice requirement—in particular, her claims for
strict liability for nonconformance with representations, breach of express warranty, and breach of
implied warranty. Thus, to the extent that the district court granted summary judgment on these
claims based on Breg’s lack of notice, Krumpelbeck argues that the court erred.
It is clear from her complaint that Krumpelbeck asserted two distinct categories of claims:
those that require notice of a foreseeable risk and those that are premised on a material

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misrepresentation.3 Having determined that Krumpelbeck’s common law claims are barred, we
address the merits of Krumpelbeck’s arguments only with respect to those claims that are cognizable
under the OPLA.
1. Claims that include a notice requirement
The claims that Krumpelbeck asserted in her complaint that require notice of a risk of harm
before liability can be imposed are: strict liability for defective design; strict liability for inadequate
warning or instruction; and negligence. Of these claims, two have statutory counterparts under the
OPLA as amended: products defective in design or formulation, found in Ohio Revised Code §
2307.75, and products defective due to inadequate warning or instruction, found in Ohio Revised
Code § 2307.76.4 Because genuine disputes of fact exist that could allow a reasonable jury to find
for Krumpelbeck on the statutory claims, we find that summary judgment was not appropriate.
a. Applicable OPLA provisions
A product is defective in design or formulation if the foreseeable risks associated with its
design or formulation exceed the benefits. Ohio Rev. Code § 2307.75(A). The foreseeable risks
associated with a product’s design are determined by considering factors, including, but not limited
to, the likely awareness of product users of the risk of harm; the likelihood of the design or

3

Krumpelbeck also correctly observes that the district court’s order focused solely on the
former category of claims (those that require notice of a foreseeable risk) and did not address the
merits of her claims based on a material misrepresentation, despite granting summary judgment in
favor of Breg on those claims.
4

The third claim, negligence, is a common law claim that has been abrogated by the OPLA.
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formulation to cause harm in light of the product’s intended or reasonably foreseeable uses; and the
extent to which the design or formulation is more dangerous than a reasonably prudent consumer
would expect when used in an intended or reasonably foreseeable manner. Id. at § 2307.75(B). A
product is defective due to inadequate warning or instruction if “the manufacturer knew, or in the
exercise of reasonable care, should have known about a risk that is associated with the product” and
the manufacturer “failed to provide the warning or instruction that a manufacturer exercising
reasonable care would have provided concerning that risk.” Id. at § 2307.76(A)(1).
b. Medical literature
According to Breg, Krumpelbeck’s claims “rest on a fundamentally flawed premise: that
Breg knew or reasonably should have known that continuous administration of anesthetic in the joint
space could cause chondrolysis.” In its motion for summary judgment, Breg averred that “no one
in the medical science community as of March 2005 had hypothesized that continuous intra-articular
infusion of anesthetic into the shoulder joint could cause chondrolysis.” Breg further argued that
“[t]his premise, still hotly disputed today, had not an iota of support in the collective literature and
knowledge of the medical scientific community when [Krumpelbeck’s] shoulder surgery was
performed.”5

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In fact, it is undisputed that it was not until March 23, 2006—one year after Krumpelbeck’s
surgery—at the annual meeting of the American Academy of Orthopedic Surgeons that Dr. Brent
Hansen discussed, for the first time, the development of chondrolysis and a possible connection to
pain pumps used in the intra-articular space. In July 2007, Dr. Hansen and his colleague Dr. Beck
published the first peer reviewed article discussing the possible link between pain pumps and
chondrolysis.
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Although liability based on defective design involves balancing the foreseeable risks against
the purported benefits, Breg’s argument fails to acknowledge the many statutory factors that a court
must consider in determining what those foreseeable risks are. See Ohio Rev. Code § 2307.75(B).
One of these factors is the so-called “consumer expectation” test, which considers “[t]he extent to
which [the product’s] design or formulation is more dangerous than a reasonably prudent consumer
would expect when used in an intended or reasonably foreseeable manner.” Id. at § 2307.75(B)(5).
This is the primary basis on which Krumpelbeck argues that Breg’s pain pump was defective in
design. The district court’s order makes only passing reference to this test, describing it as
“Plaintiff’s theory” of defective design. The district court apparently did not associate the consumerexpectation test with the OPLA; it found that Krumplebeck’s “design-defect claims fail for the same
reason [she] cannot prove her warnings claims - there is no evidence that [Breg] knew or had reason
to know of a purported risk associated with intra-articular infusion of anesthetics.” The focus of the
consumer-expectation test, however, is not the risks known to the manufacturer, but rather, the
consumer’s understanding and appreciation of the dangers associated with use of the product.
Because the district court did not discuss the statutory factors listed in § 2307.75(B), including the
consumer-expectation test, we find that it misapplied the law in determining the “foreseeable risks”
for the purposes of Krumpelbeck’s claim for defective design.
Moreover, we find that the district court’s order frames the issue too narrowly. While the
medical literature as of March 2005 was insufficient to put Breg on notice of the risk of chondrolysis
specifically, Krumpelbeck pointed to numerous articles and published studies prior to that time that
found a link between infusion of chemicals into the joint space and harm of the same general nature
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as that Krumpelbeck suffered—damage and destruction of the cartilage. The district court correctly
noted that this literature does not establish that Breg had actual notice of the risk of chondrolysis
prior to her surgery. A reasonable jury could conclude, however, that it was sufficient to put Breg
on notice of the risk of harm to the cartilage generally when its device was used to inject anesthetics
directly in the joint space. Similarly, the literature could be sufficient to put a reasonable
manufacturer on notice of the need for testing to explore the potential risks inherent in such use.
In rejecting this evidence, the district court made an impermissible factual determination that
the evidence was not sufficient, stating that it was “particularly troubled by [Krumpelbeck’s] failure
to provide any expert testimony supporting counsel’s bald conclusion that there was relevant
literature available prior to March 2005.” It is unclear why—at least, at the summary judgment
stage—the court would require Krumpelbeck to produce an expert to testify that there was relevant
literature when Krumpelbeck produced, instead, the literature itself. While a trial expert will almost
certainly be required to explain the significance of the literature to a jury, the literature itself is
evidence, more than a mere scintilla, sufficient to establish an issue for trial.

c. FDA
As additional support for her position, Krumpelbeck argues that there were other events and
circumstances that put Breg on notice of the risk of harm—in particular, the Food and Drug
Administration’s (“FDA”) refusal to approve Breg’s pain pumps for orthopedic and/or intra-articular
use. The FDA requires manufacturers, prior to marketing a medical device, to obtain either
Premarket Approval (PMA) or Premarket Notification. The latter is sought under Section 510(k)
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of the Federal Food, Drug, and Cosmetic Act, see 21 U.S.C. § 360(k), and is a significantly less
rigorous option than PMA. It is available where the manufacturer seeks approval for a medical
device that is substantially equivalent to another legally marketed, FDA-approved device. A
limitation of Section 510(k) clearance is that the FDA will only approve a new device for the
particular indications and uses for which the predicate device has been previously approved.
Continuous-infusion pain pumps have been utilized in medical practice since the 1960s, but the
evidence indicates that they have never been FDA-approved for orthopedic or intra-articular use.
On four occasions between 1998 and 2004, Breg applied for Section 510(k) approval for
various pain-pump models and included in its applications references to intra-articular and
orthopedic use. On each occasion, the FDA denied Breg’s applications because of the references to
intra-articular and/or orthopedic use, indications which had never before been approved for any of
the predicate devices Breg cited in support of its applications. The FDA would not clear the device
for these uses because Breg presented “no accompanying data to demonstrate that [the] device may
be used safely and effectively [for such] use.” Breg’s applications for FDA clearance were approved
only after all references to intra-articular/orthopedic use were deleted, and the pumps were
subsequently cleared for general surgical use.
Contrary to Krumpelbeck’s assertions, the FDA’s rejection of Breg’s § 501(k) application
was not based on any known risks of intra-articular use of pain pumps but rather on the absence of
any studies or data affirmatively establishing the safety of such use. Therefore, the FDA’s rejection
cannot give rise to a finding that Breg knew, or should have known, that its device was unsafe when

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used in the joint space because the FDA’s decision was not based on any finding that the pump was
actually unsafe when so used.
However, whether the FDA’s rejection did or should have put Breg on notice of the need to
conduct testing of its pumps to establish their safety for orthopedic and intra-articular use is another
question entirely. Had Breg elected to promote and market its pain pump only for those uses cleared
by the FDA, perhaps Breg would have no duty to conduct such testing. But there is evidence in the
record from which a jury could conclude that Breg actively marketed its products for off-label
orthopedic and/or intra-articular use without conducting any relevant safety studies.
For instance, Plaintiff’s Exhibit 57, submitted in support of Krumpelbeck’s opposition to the
motion for summary judgment, is a New Product Release for Breg’s Pain Care 4200 pump, dated
September 2002. This is an internal document, apparently directed to Breg’s sales force, which
describes the various components, features, benefits, and specifications of the 4200 pain pump.
Under the heading “Indications,” the document reads:
Designed for local wound site infusion of non-narcotic medications for postoperative pain management:
- Arthroscopic procedures
- Open Orthopedic procedures
- Combination Arthroscopic and Open orthopedic procedures
- Iliac Crest bone graft harvest sites
- General surgery
- Plastic surgery
(emphasis added). The indications clearly list orthopedic procedures, a use that the FDA expressly
informed Breg it would not approve due to Breg’s lack of data supporting the safety of such use. A
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label use without first conducting tests to establish the safety of such use. There is also Plaintiff’s
Exhibit 54, another of Breg’s internal documents submitted in support of Krumpelbeck’s opposition
to Breg’s motion. The relevant portion of this document describes placement of the pain pump
catheter and indicates that it should be placed at the origin of the pain, including around the joint
and/or directly into the joint cavity. (Sealed App. at 140.) This is further evidence from which a jury
could find that Breg actively promoted the use of its pain pumps for off-label use directly in the joint
space. Finally, Krumpelbeck’s surgeon, Dr. Paul Favorito testified that “BREG did promote the use
of intra-articular pain catheters. They never promoted them that I remember directly in the shoulder,
but I know they promoted them in the knee.”
While promoting an off-label use does not necessarily give rise to liability in itself,
promoting a use for which the safety and long-term effects have never been tested or established
might give rise to liability. Like the sufficiency of the medical literature, it is for a jury to decide
whether a reasonable manufacturer in Breg’s position would have conducted such testing prior to
promoting an off-label use of its product.
2. Claims premised on a material misrepresentation
This same evidence of off-label marketing and promotion is relevant to Krumpelbeck’s
claims that are based on a material misrepresentation, which are: strict liability for nonconformance
with representations; breach of express warranty; breach of implied warranty; negligent
misrepresentation and fraud. The bases of all of these claims is that Breg made representations
regarding the safety and quality of the pain pump and that the pain pump did not conform to these
representations because it was not safe for all uses for which Breg marketed it.
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Because they were abrogated by the 2005 amendment to the OPLA, as discussed supra, the
district court properly granted summary judgment on Krumpelbeck’s common law claims of breach
of express warranty, breach of implied warranty, and negligent misrepresentation and fraud.
However, the essence of these claims is actionable under § 2307.77 of the OPLA, which
encompasses all product liability claims based on nonconformance with a manufacturers’
representations. This provision provides that “[a] product is defective if it did not conform, when
it left the control of its manufacturer, to a representation made by that manufacturer.” Ohio Rev.
Code § 2307.77. The product may be defective even if the “manufacturer did not act fraudulently,
recklessly, or negligently in making the representation.” Id. To prevail on this claim, a plaintiff
must prove that: 1) the defendant made a representation as to a material fact regarding the character
or quality of its product; 2) the product failed to conform to the defendant’s representation; 3) the
plaintiff justifiably relied on the defendant’s representation; and 4) such reliance directly and
proximately caused the plaintiff’s alleged injuries. Miller v. ALZA Corp., 759 F. Supp. 2d 929, 942
(S.D. Ohio 2010) (citations omitted).
As noted above, there is evidence in the record from which a jury could conclude that Breg
actively promoted its device for use directly in the joint space. What the record lacks, however, is
evidence that Breg’s representatives made any express representations to Krumpelbeck—either
directly or through Dr. Favorito—regarding the safety, efficacy, or FDA approval of such use.
Krumpelbeck’s complaint avers generally that Breg “made representations regarding the character
or quality of the Breg Pain Pump, including representations that the Breg Pain Pump was safe” and
that the device did not conform to these representations. Krumpelbeck also asserted in her response
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to the motion for summary judgment that “Breg and the other manufacturers . . . falsely represent[ed]
to physicians that the FDA had approved the pumps for joint space use.” However, Krumpelbeck
has failed to identify where, to whom, or by whom these alleged representations were made, nor has
she pointed to any evidence to substantiate her allegations.
The only evidence in the record that would appear to speak to this issue is Dr. Favorito’s
deposition testimony. Dr. Favorito indicated that Breg did not warn him that intra-articular use was
not cleared by the FDA and that, at the time he was using Breg’s device in that manner, he did so
with the belief that the device had been cleared by the FDA for such use. However, Dr. Favorito did
not testify that a representative of Breg affirmatively told him that the pump had been FDA-approved
for orthopedic and/or intra-articular use. Absent some evidence showing that Breg made an express
representation to Krumpelbeck and/or her doctor regarding the safety or FDA approval of its pump
for use in the joint space, summary judgment on this claim was appropriate.6
IV. CONCLUSION
For the foregoing reasons, we AFFIRM the district court’s grant of summary judgment as
to Krumpelbeck’s claims of nonconformance with representations, negligence, breach of express
warranty, breach of implied warranty, negligent misrepresentation and fraud. We REVERSE and
REMAND for further proceedings as to Krumpelbeck’s statutory claims for defective design and
inadequate warning or instruction.

6

Aside from Krumpelbeck’s failure to show that Breg made an express representation
regarding a material fact, we note that the record is also lacking in evidence of other elements of this
claim—namely, justifiable reliance and causation.
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