Opinion

Tomlin v. Smith & Nephew, Inc.

Court
District Court, S.D. Ohio
Filed
Sep 2, 2020
Cited by
0 cases
Authority
More cited than 28.2%

“a plaintiff is deemed to have abandoned a claim when a plaintiff fails to address it in response to a motion.”

How later courts described this case

  • “a plaintiff is deemed to have abandoned a claim when a plaintiff fails to address it in response to a motion.”

Written by the judges who cited it.

The opinion

IN THE UNITED STATES DISTRICT COURT

FOR THE SOUTHERN DISTRICT OF OHIO

WESTERN DIVISION

ROLLIN TOMLIN, :

Plaintiff,

Case No. 3:19-cv-354

Vv. :

JUDGE WALTER H. RICE

SMITH & NEPHEW, INC., et a/,

Defendants. :

DECISION AND ENTRY SUSTAINING IN PART AND OVERRULING

IN PART DEFENDANT SMITH & NEPHEW, INC.’S MOTION TO

DISMISS PLAINTIFF'S COMPLAINT (DOC. #5); PLAINTIFF GIVEN

LEAVE TO AMEND COMPLAINT WITHIN 14 DAYS

Plaintiff Rollin Tomlin had a total knee replacement in 2015. His doctor

used the Journey || Total Knee System, manufactured by Defendant Smith &

Nephew, Inc. Plaintiff continued to suffer severe pain and discomfort, and had

revision surgery in 2017. He then filed suit against Smith & Nephew, alleging

numerous claims of product liability. This matter is currently before the Court on

Defendant Smith & Nephew, Inc.’s Motion to Dismiss Plaintiff's Complaint, Doc.

#5.

I. Background and Procedural History

On October 27, 2015, Rollin Tomlin underwent total knee arthroplasty. His

doctor implanted the Journey II Total Knee System (hereafter the “Product”),

designed, manufactured and distributed by Defendant Smith & Nephew, Inc.

Tomlin continued to experience pain and discomfort in his knee. Two years later,

he had revision surgery.

On October 16, 2019, Tomlin filed suit in the Montgomery County Common

Pleas Court against Smith & Nephew, and against Doe Defendants 1-100. Smith &

Nephew removed the case to federal court on the basis of diversity jurisdiction.

Tomlin essentially argues that Smith & Nephew knew, or should have known, of

problems with the Product that would cause the Product to loosen and fail. The

Complaint asserts twelve causes of action:

(I) Negligence

(Il) © Ohio Product Liability Act (“OPLA”) violations

(Ill) Strict Products Liability: OPLA— Design Defect

(IV) Strict Products Liability: OPLA—Manufacturing Defect

(V) Strict Products Liability: OPLA—Failure to Warn

(VI) Breach of Express Warranty

(VII) Breach of Implied Warranty

(VIII) Fraudulent Misrepresentation

(IX) Fraudulent Concealment

(X) Negligent Misrepresentation

(Xl) Unjust Enrichment

(XII) Punitive Damages

Doc. #3."

Defendant has moved to dismiss the Complaint in its entirety. Doc. #5.

That motion is fully briefed, Docs. ##8, 9, and ripe for decision.

As Defendant points out, the Counts are incorrectly numbered in the Complaint.

There is no Count! or Count IX, but there are two each of Counts Il and XI. The

Court has taken the liberty of renumbering the Counts and will refer to them by

their new numbers throughout this Decision and Entry.

Hl. Fed. R. Civ. P. 12(b)(6)

Federal Rule of Civil Procedure 8(a) provides that a complaint must contain

“a short and plain statement of the claim showing that the pleader is entitled to

relief.” The complaint must provide the defendant with “fair notice of what the

... Claim is and the grounds upon which it rests.” Be// Atlantic Corp. v. Twombly,

550 U.S. 544, 555 (2007) (quoting Conley v. Gibson, 355 U.S. 41, 47 (1957)).

Federal Rule of Civil Procedure 12(b)(6) allows a party to move for dismissal

of a complaint on the basis that it “fail[s] to state a claim upon which relief can be

granted.” The moving party bears the burden of showing that the opposing party

has failed to adequately state a claim for relief. DirecTV, Inc. v. Treesh, 487 F.3d

471, 476 (6th Cir. 2007) (citing Carver v. Bunch, 946 F.2d 451, 454-55 (6th Cir.

1991)). The purpose of a motion to dismiss under Rule 12(b)(6) “is to allow a

defendant to test whether, as a matter of law, the plaintiff is entitled to legal relief

even if everything alleged in the complaint is true.” Mayer v. Mylod, 988 F.2d 635,

638 (6th Cir. 1993). In ruling on a 12(b)(6) motion, a court must “construe the

complaint in the light most favorable to the plaintiff, accept its allegations as true,

and draw all reasonable inferences in favor of the plaintiff.” Handy-Clay v. City of

Memphis, 695 F.3d 531, 538 (6th Cir. 2012) (quoting 7reesh, 487 F.3d at 476).

Nevertheless, to survive a motion to dismiss under Rule 12(b)(6), the

complaint must contain “enough facts to state a claim to relief that is plausible on

its face.” Twombly, 550 U.S. at 570. Unless the facts alleged show that the

plaintiff's claim crosses “the line from conceivable to plausible, [the] complaint

must be dismissed.” /d. Although this standard does not require “detailed factual

allegations,” it does require more than “labels and conclusions” or “a formulaic

recitation of the elements of a cause of action.” /d. at555. “Rule 8... does not

unlock the doors of discovery for a plaintiff armed with nothing more than

conclusions.” Ashcroft v. /qba/, 556 U.S. 662, 678-79 (2009). Legal conclusions

“must be supported by factual allegations” that give rise to an inference that the

defendant is, in fact, liable for the misconduct alleged. /d. at 679.

lil. Analysis

Plaintiff seeks recovery under a wide variety of theories. However, as the

Complaint states, “[e]ach and every one of Plaintiff's claims for damages relate to

Defendants’ design, manufacture, sale, testing, marketing, labeling, advertising,

promotion, and/or distribution of the Product.” Doc. #3, PagelD#66.

A. OPLA Abrogates All Common Law Claims

Defendant argues that Plaintiff’s common law claims of negligence, breach

of express warranty, breach of implied warranty, fraudulent misrepresentation,

fraudulent concealment, negligent misrepresentation, and unjust enrichment

(Counts | and VI-XI) must be dismissed because they are expressly abrogated by

the Ohio Products Liability Act (“OPLA”), Ohio Revised Code § 2307.71(B). That

statute provides that "Sections 2307.71 to 2307.80 of the Revised Code are

intended to abrogate all common law product liability claims or causes of action."

Ohio Rev. Code 8 2307.71(B).

1. Negligence, Fraudulent Misrepresentation, Fraudulent

Concealment, Unjust Enrichment (Count I, VIII, IX, X1)

By not responding to Defendant's argument, Plaintiff impliedly concedes

that the claims for negligence, fraudulent misrepresentation, fraudulent

concealment, and unjust enrichment are abrogated by the OPLA. See Brown v.

VHS of Michigan, Inc., 545 F. App’x 368, 372 (6th Cir. 2013) (“a plaintiff is deemed

to have abandoned a claim when a plaintiff fails to address it in response to a

motion.”). On this basis, the Court SUSTAINS Defendant's Motion to Dismiss

Counts I, VIll, IX and XI, and dismisses these Counts with prejudice.?

2. Breach of Express and Implied Warranty (Counts VI and VII)

Plaintiff concedes that his claims for breach of express and implied

warranty are also subsumed by the OPLA. Nevertheless, he argues that, rather

than dismiss these claims, the Court should grant him leave to amend his

Complaint to assert these claims under Ohio Revised Code 8 2307.77, the OPLA

provision governing products defective due to nonconformance with

manufacturers’ representations.°®

2 Defendant also argues that the claims of fraudulent misrepresentation and

fraudulent concealment must be dismissed because Plaintiff has failed to plead

these claims with the particularity required by Fed. R. Civ. P. 9(b). Given the

Court’s finding that these claims are abrogated by the OPLA, the Court does not

reach this other argument.

3 That statute 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. A product may be defective because it did not conform to a

representation even though its manufacturer did not act fraudulently, recklessly,

or negligently in making the representation." Ohio Rev. Code 8 2307.77.

A plaintiff seeking to recover under 8 2307.77 must prove:

(1) that the manufacturer made a representation as to a

material fact concerning the character or quality of the

manufacturer's product;

(2) that the product did not conform to that representation;

(3) that the plaintiff justifiably relied on that representation; and

(4) that the plaintiff's reliance on the representation was the

direct and proximate cause of the plaintiff's injuries.

Gawloski v. Miller Brewing Co., 96 Ohio App. 3d 160, 165, 644 N.E.2d 731, 734

(1994).

Defendant argues that any such amendment would be futile because

Plaintiff has not alleged sufficient facts indicating that the Product was defective or

how it failed to conform to a representation made by Defendant. The Court

rejects this argument. Plaintiff has alleged that Defendant expressly warranted

that the Product was safe and effective, was of merchantable quality, that it had

no dangerous side effects, and that it was adequately tested and fit for its

intended use. He has further alleged that the Product did not conform to these

representations in that it caused him serious injury, including severe pain and the

need for revision surgery, that he and his physician justifiably relied on

Defendant's representations, and that such reliance was the proximate cause of

his injuries. Doc. #3, PagelD##86-89.

Given that Plaintiff's common law claims of breach of express and implied

warranty are abrogated by the OPLA, the Court SUSTAINS Defendant’s Motion to

Dismiss Counts VI and VIl. Nevertheless, within 14 days of the date of this

Decision and Entry, Plaintiff may amend his Complaint to replead these two

claims under the OPLA, mindful of the strictures of Fed. R. Civ. P. 11.

3. Negligent Misrepresentation (Count X)

In Count X of the Complaint, Plaintiff alleges that Defendant had a duty to

tell the medical community, the FDA and consumers the truth about the safety

and effectiveness of the Product, that Defendant breached this duty by

intentionally concealing the truth and failing to warn about the defective condition

of the Product, that he and his physician justifiably relied on Defendant's

representations, and that he was injured as a result. Doc. #3, PagelD##96-98.

Defendant argues that this negligent misrepresentation claim is abrogated by the

OPLA.

Citing Hogue v. Pfizer, Inc., 893 F. Supp. 2d 914, 918 (S.D. Ohio 2012)

(Watson, J.), vacated in part on other grounds, No. 2:10-cv-805, 2013 WL 12368615

(S.D. Ohio Sept. 5, 2013), Plaintiff argues that, although the OPLA abrogates

negligent misrepresentation claims that are based on a failure to warn, it does not

abrogate negligent misrepresentation claims that are based on active deception.

He maintains that his claim involves active deception in that Defendant made false

representations concerning the Product and failed to disclose material information

concerning the Product's safety and effectiveness.

The Court disagrees. The essence of Plaintiff's claim is a failure to warn

about the risks associated with the Product. As in Hogue, it is “based on a theory

of omission and concealment.” /d. at 919. It is, therefore, abrogated by the OPLA.

On this basis, the Court SUSTAINS Defendant's Motion to Dismiss Count X, the

negligent misrepresentation claim, and dismisses this claim with prejudice.

B. OPLA Claims (Counts Il, Ill, IV, V)

Plaintiff has asserted four claims under the OPLA: (1) Supplier Liability

under Ohio Revised Code § 2307.78 (Count Il); (2) Strict Liability for Design Defect

under Ohio Revised Code § 2307.75 (Count Ill); (3) Strict Liability for

Manufacturing Defect under Ohio Revised Code § 2307.74 (Count IV); and (4) Strict

Liability for Failure to Warn under Ohio Revised Code 8 2307.76 (Count V).

Defendant argues that, under the pleading standards set forth in /gbal//TwombIly,

Plaintiff has failed to state a claim upon which relief may be granted.

1. Supplier Liability (Count Il)

Count Il is broadly entitled “Ohio Product Liability Act Claims.” As

Defendant notes, it appears to encompass a variety of theories of liability,

including negligence. Plaintiff alleges that Defendant failed to exercise reasonable

care in the design, research, manufacture, marketing, testing, advertisement,

supply, promotion, packaging, sale and distribution of the Product. Doc. #3,

PagelD#71. As Defendant notes, these general allegations of negligence appear to

be duplicative of other claims asserted in the Complaint. Plaintiff does not rebut

this argument.

Count Il, however, also alleges that Defendant is liable as a “supplier” of

the Product under Ohio Revised Code § 2307.78(A)(2), because the Product did not

conform, when it left the control of Defendant, to representations made by

Defendant, and because that representation and the failure to conform to it, were

a proximate cause of Plaintiff's damages.

Plaintiff has alleged that Defendant is both a manufacturer and a supplier of

the Product. Defendant correctly points out, however, that Plaintiff cannot

proceed against a manufacturer under a theory of supplier liability. Ohio Revised

Code § 2307.71(A)(15)(b)(i) states that a “supplier” does not include a

“manufacturer.” See a/so Frey v. Novartis Pharm. Corp., 642 F. Supp. 2d 787, 795

(S.D. Ohio 2009) (Weber, J.) (holding that, because plaintiffs alleged that Novartis

was the manufacturer, they could not proceed under a theory of supplier liability).

On this basis, the Court SUSTAINS Defendant’s Motion to Dismiss Count Il, and

dismisses that claim with prejudice.

2. Design Defect (Count III)

Count Ill alleges a design defect under Ohio Revised Code 8 2307.75. That

statute provides that "a product is defective in design or formulation if, at the time

it left the control of its manufacturer, the foreseeable risks associated with its

design or formulation... exceeded the benefits associated with that design or

formulation. .." Ohio Rev. Code 8 2307.75.

Defendant argues that Plaintiff has failed to plead the necessary elements of

a product liability claim: “(1) the existence of a defect in the product at issue, (2)

that the defect existed at the time the product left the hands of the manufacturer,

and (3) the defect was the direct and proximate cause of the plaintiff's injury.”

Jones v. Statibli Motor Sports Div. of Statibli Am. Corp., 897 F. Supp. 2d 599, 607

(S.D. Ohio 2012) (Frost, J.). Defendant maintains that the Complaint is devoid of

factual allegations concerning how the Product was allegedly defective and how

the alleged defect was the direct and proximate cause of his injuries.

The Court rejects this argument. Plaintiff alleges that the Product is

defective in design because it uses oxidized zirconium rather than cobalt or

titanium. The oxidized zirconium combines metal and ceramic. Plaintiff alleges

that the ceramic is weak and brittle and difficult to fabricate into the necessary

shapes, causing the Product to have poor shock resistance, be easily damaged

and easily wear out. Doc. #3, PagelD#77. Plaintiff further alleges that this defect

existed when the Product left the hands of the manufacturer, and that it was the

direct and proximate cause of his personal injuries. /d, at PagelD##76, 78.

The Court concludes that Plaintiff has stated a plausible claim of a design

defect under Ohio Revised Code § 2307.75. Defendant’s Motion to Dismiss Count

Ill is OVERRULED.

3. Manufacturing Defect (Count IV)

Count IV of the Complaint alleges a manufacturing defect under Ohio

Revised Code § 2307.74. The statute provides that "[a] product is defective in

manufacture or construction if, when it left the control of its manufacturer, it

deviated in a material way from the design specifications, formula, or

performance standards of the manufacturer, or from otherwise identical units

10

manufactured to the same design specifications, formula, or performance

standards." Ohio Rev. Code 8 2307.74.

Although Plaintiff generally alleges that the Product “deviated from

manufacturing standards when it came off the production line,” and that it “failed

to perform in its intended manner,” resulting in Plaintiff's injuries, he fails to

identify what the manufacturing defect is. Defendant argues that Plaintiff has

failed to state a plausible claim for relief.

Citing Jones, 897 F. Supp. 2d at 610, Plaintiff argues that a manufacturing

defect may be inferred from the Product's unsafe, unexpected performance. In

Jones, however, there was evidence of a specific manufacturing defect. As

designed, a socket in a race car re-fueling system should have disengaged when

the plaintiff released the handle, but it did not. See /d. In contrast, Plaintiff has

not alleged how the Product implanted in his knee deviated from any

manufacturing standards.

Plaintiff also cites to Creech v. Emerson Climate Techs., Inc., No. 3:15-cv-14,

2015 U.S. Dist. LEXIS 147087, at *8 (S.D. Ohio Oct. 28, 2015) (Rice, J.), in which

this Court noted that, even though plaintiff had not yet identified a specific

manufacturing defect, details concerning the exact nature of such a defect are

typically in the defendant's exclusive control, making them difficult to ascertain

prior to discovery. Nevertheless, in Creech, the Court granted leave to amend

because the plaintiff had already hired an expert witness who opined that a

manufacturing defect existed.

1]

The Court agrees with Defendant that Plaintiff's allegations of a

manufacturing defect are simply too conclusory to state a plausible claim under

Ohio law. The Complaint contains no factual allegations to support a claim that

the Product implanted in Plaintiff deviated in a material way from Defendant's

design specifications or performance standards, or from otherwise identical units

manufactured to the same design specifications or performance standards. See,

e.g., Frey, 642 F. Supp. 2d at 795 (dismissing manufacturing defect claim where

plaintiffs did “nothing more than provide a formulaic recitation of the elements of

a claim under the statute” and “failed to allege any facts that would permit the

Court to conclude that a manufacturing defect occurred and that the defect was

the proximate cause of [the] alleged injuries.”).

The Court therefore SUSTAINS Defendant's Motion to Dismiss Count IV, but

dismisses this claim without prejudice. Given that the Court is already giving

Plaintiff the opportunity to amend his Complaint to assert an OPLA claim under

Ohio Revised Code 8 2307.77 (product defective due to nonconformance with

manufacturers’ representations), the Court will likewise give Plaintiff the

opportunity to amend his manufacturing defect claim within 14 days, if he can do

so within the bounds of Fed. R. Civ. P. 11.

4. Failure to Warn (Count V)

Count V of the Complaint asserts a claim of failure to warn under Ohio

Revised Code § 2307.76(A). That statute provides:

12

(A) Subject to divisions (B) and (C) of this section, a product is

defective due to inadequate warning or instruction if either of the

following applies:

(1) It is defective due to inadequate warning or

instruction at the time of marketing if, when it left the

control of its manufacturer, both of the following

applied:

(a) The manufacturer knew or, in the

exercise of reasonable care, should have

known about a risk that is associated with

the product and that allegedly caused harm

for which the claimant seeks to recover

compensatory damages;

(b) The manufacturer failed to provide the

warning or instruction that a manufacturer

exercising reasonable care would have

provided concerning that risk, in light of the

likelihood that the product would cause

harm of the type for which the claimant

seeks to recover compensatory damages

and in light of the likely seriousness of that

harm.

(2) It is defective due to inadequate post-marketing

warning or instruction if, at a relevant time after it left

the control of its manufacturer, both of the following

applied:

(a) The manufacturer knew or, in the

exercise of reasonable care, should have

known about a risk that is associated with

the product and that allegedly caused harm

for which the claimant seeks to recover

compensatory damages;

(b) The manufacturer failed to provide the

post-marketing warning or instruction that a

manufacturer exercising reasonable care

would have provided concerning that risk,

in light of the likelihood that the product

would cause harm of the type for which the

claimant seeks to recover compensatory

damages and in light of the likely

seriousness of that harm.

13

Ohio Rev. Code 8 2307.76(A).

Plaintiff alleges that, despite knowing of the defective condition of the

Product, Defendant failed to adequately warn the medical community and

consumers about the risks associated with the use of the Product. Plaintiff further

alleges that, if he had received an adequate warning, he would not have used the

Product and would not have suffered harm. Doc. #3, PagelD##82-85.

Defendant cites to the “learned intermediary” doctrine, codified in Ohio

Revised Code 8 2307.76(C):

An ethical drug is not defective due to inadequate warning or

instruction if its manufacturer provides otherwise adequate warning

and instruction to the physician or other legally authorized person

who prescribes or dispenses that ethical drug for a claimant in

question and if the federal food and drug administration has not

provided that warning or instruction relative to that ethical drug is to

be given directly to the ultimate user of it.

Ohio Rev. Code 8 2307.76(C). This “learned intermediary” doctrine has been

extended to warnings about medical devices. Vaccariello v. Smith & Nephew

Richards, Inc., 94 Ohio St. 3d 380, 384, 763 N.E.2d 160, 164 (2002).

Defendant maintains that Plaintiff's claim is subject to dismissal because he

failed to plead how the warning given was inadequate for his physician, what

warnings were provided to his physician, what different warning to his physician

would have been appropriate or adequate, and whether the physician had any

independent knowledge of the risks associated with the Product.

14

The Court disagrees. Under Ohio law, the “learned intermediary” doctrine

is a defense to a failure-to-warn claim. Boyd v. Lincoln Elec. Co., 179 Ohio App.3d

559, 2008-Ohio-6143, 902 N.E.2d 1023, at 953. Because a plaintiff is “not required

to plead around all potential defenses,” dismissal at this stage would be

premature. See McDaniel v. Upsher-Smith Labs., Inc., 893 F.3d 941, 950-51 (6th

Cir. 2018) (Cole, C.J., concurring in part and dissenting in part). Accordingly, the

Court OVERRULES Defendant's Motion to Dismiss Count V.

C. Punitive Damages (Count XIl)

Plaintiff also seeks punitive damages. Defendant argues that because an

award of punitive damages is derivative, and all other counts are subject to

dismissal, this claim must be dismissed as well. Given that some of Plaintiff's

claims survive the Motion to Dismiss, the Court OVERRULES Defendant's Motion

to Dismiss Count XIl.

IV. Conclusion

For the reasons set forth above, the Court SUSTAINS IN PART and

OVERRULES IN PART Defendant Smith & Nephew, Inc.’s Motion to Dismiss

Plaintiff's Complaint. Doc. #5.

The Court DISMISSES WITH PREJUDICE Plaintiff's claims of negligence

(Count |), fraudulent misrepresentation (Count VIII), fraudulent concealment

(Count IX), negligent misrepresentation (Count X) and unjust enrichment (Count

because they are abrogated by the OPLA. Although Plaintiff's claims of

15

breach of express and implied warranty (Counts VI and VII) are also abrogated by

the OPLA, they are DISMISSED WITHOUT PREJUDICE. Within 14 days of the date

of this Decision and Entry, Plaintiff is given leave to amend his Complaint to

replead these claims under the OPLA if he can do so within the bounds of Fed. R.

Civ. P. 11.

Although Plaintiff has failed to state a plausible claim of a manufacturing

defect under the OPLA (Count IV), the Court DISMISSES this claim WITHOUT

PREJUDICE. Again, within 14 days of the date of this Decision and Entry, Plaintiff

may amend his Complaint to cure the insufficiencies discussed above, but only if

he can do so within the strictures of Fed. R. Civ. P. 11.

The Court SUSTAINS Defendant's Motion to Dismiss the claim of supplier

liability under the OPLA (Count Il) and DISMISSES this claim WITH PREJUDICE.

The Court OVERRULES the Motion to Dismiss the OPLA claims of design

defect (Count Ill) and failure to warn (Count V). The Court also OVERRULES the

Motion to Dismiss the claim for punitive damages (Count XIl).

To summarize, subject to the filing of an Amended Complaint on those

claims dismissed herein without prejudice, Plaintiff may proceed on his claims of

design defect (Count Ill), manufacturing defect (Count IV), failure to warn (Count

V), breach of express warranty (Count VI), breach of implied warranty (Count VII)

and punitive damages (Count XIl).

16

LJotune >). Rie

Date: September 2, 2020

WALTER H. RICE

UNITED STATES DISTRICT JUDGE

17

This is a copy of a public record, reproduced as it was published. It is not legal advice, and it may not be the version a court would rely on. Check the official source before you cite it.

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