Soutner v. Covidien, LP.

CourtDistrict Court, M.D. Pennsylvania
DecidedAugust 13, 2019
Docket1:17-cv-02178
StatusUnknown

This text of Soutner v. Covidien, LP. (Soutner v. Covidien, LP.) is published on Counsel Stack Legal Research, covering District Court, M.D. Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Soutner v. Covidien, LP., (M.D. Pa. 2019).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE MIDDLE DISTRICT OF PENNSYLVANIA

RONALD SOUTNER & JANELLE : SOUTNER, : Plaintiffs : No. 1:17-cv-02178 : v. : (Judge Kane) : COVIDIEN, LP, : Defendant :

MEMORANDUM Before the Court is Defendant Covidien, LP (“Defendant”)’s motion to dismiss Plaintiffs Ronald Soutner and Janelle Soutner’s (“Plaintiffs”) second amended complaint (Doc. No. 24), pursuant to Federal Rule of Civil Procedure 12(b)(6) (Doc. No. 25). For the reasons provided herein, the Court will grant Defendant’s motion. I. BACKGROUND1 Defendant is a Delaware limited partnership headquartered in Mansfield, Massachusetts, engaged in the design, manufacture, and sale of medical devices, including various surgical meshes. (Doc. No. 24 ¶¶ 3-5.) One such mesh, Parietex ProGrip Mesh, used in hernia repair

1 The following background is taken from Plaintiffs’ second amended complaint. (Doc. No. 24.) The allegations set forth in the amended complaint are accepted as true for the purpose of the instant motion to dismiss. See Schuylkill Energy Res., Inc. v. Pa. Power & Light Co., 113 F.3d 405, 417 (3d Cir. 1997) (explaining that “[w]hen reviewing a 12(b)(6) dismissal, [the Court] must accept as true the factual allegations in the complaint and all reasonable inferences that can be drawn from them”). The Court observes that Plaintiff’s second amended complaint (Doc. No. 24) contains factual averments identical to those set forth in their amended complaint, with the exception of the sections entitled “Plaintiff Specific Facts” (id. at 8) and “Estoppel [f]rom Pleading Statutes of Limitations or Repose” (id. at 11). As a result, this background is substantially similar to the background provided in the Court’s Memorandum dated October 26, 2018 (Doc. No. 22), issued in connection with an Order denying Defendant’s motion to dismiss Plaintiff’s amended complaint without prejudice (Doc. No. 12). surgeries, was implanted in Plantiff Ronald Soutner (“Soutner”) during a surgical procedure on December 20, 2011, and is the subject of the instant action. (Id. ¶ 4.) Hernias are caused by the “penetration of fatty tissue, intestine, or organs through a weakened or compromised location in muscle of [sic] connective tissue.” (Id. ¶ 13.) As stated in

the second amended complaint, hernia repairs are “common surgeries” – they are performed in the United States more than one million times each year – and inguinal hernia repairs make up approximately 80% of those procedures. (Id. ¶ 17.) Surgical mesh, including Defendant’s Parietex ProGrip Mesh, is used during hernia repair surgeries to “strengthen the repair.” (Id. ¶ 19.) Defendant’s Parietex ProGrip Mesh is intended for permanent implantation in a patient’s body. (Id. ¶ 6.) According to Plaintiffs, unlike most hernia mesh products, which are polypropylene based, Defendant’s Parietex ProGrip Mesh is made of monofilament polyester, which Plaintiffs allege is “flimsy” compared to polypropylene. (Id. ¶¶ 31, 42.) Plaintiffs aver that, as a result, surgeons reported difficulty in handling Defendant’s Parietex ProGrip Mesh during hernia repair

surgeries. (Id. ¶ 43.) Plaintiffs state that to remedy this issue, Defendant added a layer of collagen to the Parietex ProGrip Mesh, which was intended to make the mesh easier to handle during surgeries. (Id. ¶ 44.) In addition, Plaintiffs allege that Defendant attached micro-grips to the Parietex ProGrip Mesh to prevent the mesh from tearing. (Id. ¶¶ 46-47.) Plaintiffs further aver that the micro-grips have caused patients who have been implanted with the Parietex ProGrip Mesh to experience “debilitating pain” due to the Parietex ProGrip Mesh “contracting and pulling on all of the tissues and nerves upon which it is attached.” (Id. ¶ 48.) On December 20, 2011, Soutner underwent surgery to repair an inguinal hernia on the left side of his groin. (Id. ¶ 50.) During this procedure, Defendant’s Parietex ProGrip Mesh was implanted into Soutner to “reinforce tissue affected by the hernia.” (Id. ¶¶ 50, 52.) At some point following the procedure, Soutner experienced severe inflammation in the region where the procedure was performed. (Id. ¶ 55.) According to Plaintiffs, the inflammation was so severe that Soutner’s vas deferens was “destroyed.” (Id.) On October 7, 2013, Soutner underwent an

additional surgical procedure, at which time Defendant’s Parietex ProGrip Mesh was removed. (Id. ¶ 53.) During the second procedure, it was determined that “Defendant’s Parietex ProGrip Mesh integrated to the surrounding muscles where it had to be dissected off.” (Id. ¶¶ 53-54.) During this second procedure, Soutner’s vas deferens was removed. (Id. ¶ 55.) Plaintiffs allege that, following the second procedure, Soutner has experienced and continues to experience groin pain and life without his vas deferens. (Id. ¶ 57.) Plaintiffs further allege that as a direct and proximate result of the implanted mesh products, Soutner “suffered, is suffering, and/or will continue to suffer the abovementioned injuries, including the risk of malfunction, decreased efficacy, recurrent hernia, perforation of tissue and/or organs, adherence to tissue/organs, infection, nerve damage, subsequent surgeries, and other complications.” (Id. ¶ 65.)

Plaintiffs allege that Soutner, through the exercise of reasonable diligence, could not have discovered his injury was caused by Defendant’s mesh product because his physicians “were not informed by Defendant that these injuries could result from the implantation of Defendant[’]s faulty mesh product.” (Id. ¶ 59.) Plaintiffs further allege that Soutner “did not know and could not have known that he was injured and that his injuries were caused by Defendant’s defective product until he saw a commercial in 2017 which enlightened him to the fact that he was, in fact, injured and that his injuries could have been caused by the conduct of another.” (Id. ¶ 62.) Plaintiffs also allege that Soutner is “not employed in the medical field and was not privy to the same sophisticated medical information as Defendant, who negligently and fraudulently concealed the fact that these injuries could, and did in fact, result from its defective mesh product.” (Id. ¶ 61.) After experiencing the injuries described supra, Soutner commenced this action by filing a complaint against Defendant on October 27, 2017, in the Court of Common Pleas of Dauphin

County, Pennsylvania. (Doc. No. 1 at 10.) In his initial complaint, Soutner asserted the following ten claims against Defendant: strict liability based on defective design and manufacture (Count I); strict liability due to a failure to warn (Count II); negligence (Count III); breach of warranty (Count IV); fraudulent misrepresentation (Count V); negligent misrepresentation (Count VI); unjust enrichment (Count VII); breach of express warranty (Count VIII); breach of implied warranty of merchantability (Count IX); and breach of implied warranty of fitness (Count X). (Id. at 21-36.) On November 28, 2017, Defendant removed the action to this Court pursuant to 28 U.S.C. §§ 1441 and 1446. (Id. at 2.) Soutner filed an amended complaint on January 12, 2018, adding his wife Janelle Soutner as a plaintiff and asserting additional claims for punitive damages (Count XI), and loss of consortium (Count XII). (Doc.

No.

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