Taylor v. Smith & Nephew, Inc.

CourtDistrict Court, S.D. Mississippi
DecidedDecember 5, 2019
Docket3:18-cv-00234
StatusUnknown

This text of Taylor v. Smith & Nephew, Inc. (Taylor v. Smith & Nephew, Inc.) is published on Counsel Stack Legal Research, covering District Court, S.D. Mississippi primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Taylor v. Smith & Nephew, Inc., (S.D. Miss. 2019).

Opinion

UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF MISSISSIPPI NORTHERN DIVISION

JOHN RANDOLPH TAYLOR PLAINTIFF

V. CIVIL ACTION NO. 3:18-CV-234-DPJ-JCG

SMITH & NEPHEW, INC. DEFENDANT

ORDER In this product-liability action, Defendant Smith & Nephew, Inc. (“S&N”) moved to dismiss the Complaint under Federal Rules of Civil Procedure 8 and 12(b)(6). Plaintiff John Randolph Taylor subsequently sought leave to file a Fourth Amended Complaint. For the following reasons, Defendant’s motion [54] is granted in part and moot in part, Plaintiff’s motions [57, 59] are granted in part and denied in part, and Plaintiff is directed to file an amended complaint consistent with this Order. I. Background This case arises from a hip-replacement surgery gone awry. Taylor received a hip implant, the components of which were “designed, manufactured, distributed, sold and/or placed into the stream of commerce” by S&N. Pl.’s Third Am. Compl. [23] ¶ 8. The implant only caused him more pain, so Taylor underwent a second surgery. Id. ¶ 9. As a result of these operations, Taylor filed suit against S&N alleging several product-liability claims. See id. ¶¶ 11– 18. Taylor now seeks to amend his complaint to clarify those claims. S&N concedes that the Proposed Fourth Amended Complaint “cure[s] some deficiencies in [Taylor’s] pleadings, and the issues have been narrowed,” but challenges the amendment as to Taylor’s manufacturing-defect and implied-warranty claims. Def.’s Resp. [65] at 4; see also Def.’s Reply [70] at 2–3. II. Standard Federal Rule of Civil Procedure 15(a)(1)(A) allows a party to amend a pleading as a matter of course within 21 days of serving the pleading. A party may amend a pleading outside this three-week window “only with the opposing party’s written consent or the court’s leave.” Fed. R. Civ. P. 15(a)(2). The rule instructs that “[t]he court should freely give leave when justice

so requires.” Id. Indeed, “Rule 15(a) evinces a bias in favor of granting leave to amend.” Thomas v. Chevron U.S.A., Inc., 832 F.3d 586, 590 (5th Cir. 2016) (quoting Herrmann Holdings, Ltd v. Lucent Techs., Inc., 302 F.3d 552, 566 (5th Cir. 2002)) (internal quotation marks omitted). “It is settled that the grant of leave to amend the pleadings pursuant to Rule 15(a) is within the discretion of the trial court.” Zenith Radio Corp. v. Hazeltine Research, Inc., 401 U.S. 321, 330 (1971). But “it is by no means automatic.” Wimm v. Jack Eckerd Corp., 3 F.3d 137, 139 (5th Cir. 1993) (quoting Addington v. Farmer’s Elevator Mut. Ins. Co., 650 F.2d 663, 666 (5th Cir. 1981)) (internal quotation marks omitted). Accordingly, “the district court may consider such factors as undue delay, bad faith or dilatory motive on the part of the movant,

repeated failure to cure deficiencies by amendments previously allowed, undue prejudice to the opposing party, and futility of amendment.” Id. A futility analysis is “identical, in practice, to the standard used for reviewing a dismissal under Rule 12(b)(6).” Thomas, 832 F.3d at 590 (quoting City of Clinton v. Pilgrim’s Pride Corp., 632 F.3d 148, 152 (5th Cir. 2010)). That is, the Fifth Circuit has interpreted “futility” to mean that “the amended complaint would fail to state a claim upon which relief could be granted.” Stripling v. Jordan Prod. Co., LLC, 234 F.3d 863, 873 (5th Cir. 2000). Under the well-known Rule 12(b)(6) standard, “a complaint must contain sufficient factual matter, accepted as true, to ‘state a claim to relief that is plausible on its face.’” Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009) (quoting Bell Atlantic Corp v. Twombly, 550 U.S. 544, 570 (2007)). “A claim is facially plausible if the complaint ‘allows the court to draw the reasonable inference that the defendant is liable for the misconduct alleged.” Id. III. Analysis S&N’s motion to dismiss originally challenged Taylor’s Third Amended Complaint.

Although Taylor seeks to amend the Third Amended Complaint, the Proposed Fourth Amended Complaint contains the same previously-challenged claims, just with more detail, and S&N’s arguments rest on the same grounds. Accordingly, they will be addressed collectively. A. Manufacturing-Defect Claim In his Proposed Fourth Amended Complaint, Taylor alleges that the components in his hip implant “were defective in design and/or manufacture.” Pl.’s Proposed Fourth Am. Compl. [59-1] ¶¶ 12, 15. S&N argues that the proposed complaint “does not identify which components deviated from specification” or “describe the alleged deviation[.]” Def.’s Resp. [65] at 4. Taylor replies that the complaint is sufficient, and he should be allowed to proceed to discovery to be

more specific. Pl.’s Reply [71] at 3. In Mississippi, the Mississippi Products Liability Act (“MPLA”) “provides the exclusive remedy for products-liability claims[.]” Elliot v. El Paso Corp., 181 So. 3d 263, 268 (Miss. 2015) (footnote and internal quotation marks omitted). The MPLA applies “in any action for damages caused by a product, including, but not limited to, any action based on a theory of strict liability in tort, negligence or breach of implied warranty, except for commercial damage to the product itself[.]” Miss. Code Ann. § 11-1-63. For manufacturing-defect claims, the statute provides that the plaintiff must show that, “at the time the product left the control of the manufacturer,” (i) . . . The product was defective because it deviated in a material way from the manufacturer’s or designer’s specifications or from otherwise identical units manufactured to the same manufacturing specifications[;] . . . (ii) The defective condition rendered the product unreasonably dangerous to the user or consumer; and (iii) The defective and unreasonably dangerous condition of the product proximately caused the damages for which recovery is sought. Id. § 11-1-63(a). In other words, “manufacturing defect claims involve allegations not that the entire product line in question was defectively designed, but rather that the specific product purchased by the consumer was manufactured in a way which deviated from the design specifications.” Hickory Springs Mfg. Co. v. Star Pipe Prods., Ltd., 991 F. Supp. 2d 778, 780 (N.D. Miss. 2014). Accordingly, “a plaintiff must ‘allege how the subject product(s) deviated from the manufacturers’ specifications or other units.’” Little v. Smith & Nephew, Inc., No. 1:15-CV-00028-GHD-DAS, 2015 WL 3651769, at *8 (N.D. Miss.

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Taylor v. Smith & Nephew, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/taylor-v-smith-nephew-inc-mssd-2019.