Hammons, P. v. Ethicon, Inc., Aplts.

CourtSupreme Court of Pennsylvania
DecidedOctober 21, 2020
Docket7 EAP 2019
StatusPublished

This text of Hammons, P. v. Ethicon, Inc., Aplts. (Hammons, P. v. Ethicon, Inc., Aplts.) is published on Counsel Stack Legal Research, covering Supreme Court of Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Hammons, P. v. Ethicon, Inc., Aplts., (Pa. 2020).

Opinion

[J-2-2020] IN THE SUPREME COURT OF PENNSYLVANIA EASTERN DISTRICT

SAYLOR, C.J., BAER, TODD, DONOHUE, DOUGHERTY, WECHT, MUNDY, JJ.

PATRICIA L. HAMMONS : No. 7 EAP 2019 : : Appeal from the Order of Superior v. : Court entered on June 19, 2018 at : No. 1526 EDA 2016 (reargument : denied August 29, 2018) affirming ETHICON, INC. AND JOHNSON & : the Judgment of the Court of JOHNSON; GYNECARE; SECANT : Common Pleas, Philadelphia MEDICAL; SECANT MEDICAL INC.; : County, Civil Division entered on PRODESCO, INC.; AND SECANT : April 14, 2016 at No. 3913 May MEDICAL, LLC : Term, 2013. : : ARGUED: March 10, 2020 APPEAL OF: ETHICON, INC. AND : JOHNSON & JOHNSON :

OPINION

JUSTICE BAER DECIDED: October 21, 2020 This case presents a challenge to the exercise of specific personal jurisdiction in

Pennsylvania over New Jersey corporate defendants in a case filed by an Indiana

resident regarding injuries allegedly caused by a pelvic mesh medical device implanted

in Indiana. While the device was assembled by the defendants out of state, the mesh

component of the device was manufactured by a separate entity in Pennsylvania. After

reviewing recent decisions from the United States Supreme Court revising its personal

jurisdiction jurisprudence, we conclude that the imposition of personal jurisdiction in this

case meets the relevant constitutional and statutory requirements. Accordingly, we affirm

the judgment of the Superior Court.

I. Factual and Procedural History Appellee-Plaintiff Patricia Hammons (“Hammons”) is an Indiana resident who

suffered significant injuries following the May 2009 implantation in Indiana of Appellant-

Defendant Ethicon, Inc.’s Prolift Kit, which is a medical device used to treat “medical

conditions in the female pelvis, primarily pelvic organ prolapse and/or stress urinary

incontinence.” Plaintiffs’ Master Long Form Complaint (“Master Complaint”) at ¶ 23. She

received treatment for the injuries in Indiana and Kentucky.1

The Prolift Kit includes mesh, which has been cut to a specific shape, along with

tools to implant it and instructions. The mesh is “woven from filaments of polypropylene

and/or other non-biological substances designed and intended to be permanently

implanted through surgery in the human body.” Id.

As is relevant to the jurisdictional question before us, all parties agree that the

mesh is the only aspect of the Prolift Kit produced in Pennsylvania. Ethicon contracted

with Secant Medical, Inc. (“Secant”), a Bucks County manufacturer, to weave the mesh

according to Ethicon’s specifications from Ethicon’s proprietary polypropylene filament.

As the characteristics of the mesh and the production process are central to the issues in

this case, we set forth the details as described in an affidavit by a Secant officer:

Ethicon supplies Secant with spools of PROLENE™ polypropylene filament, which Secant, in response to purchase orders, knits to produce large rolls of mesh per specifications provided and required by Ethicon. Ethicon’s specifications govern various characteristics of the mesh, including its elasticity, density, mass, and areal density. Ethicon establishes the specifications for the knitting of the mesh component[,] and Secant is required to follow these specifications. Once the PROLENE™ polypropylene filaments are knit into mesh, samples of the mesh are

1 As our review of this case is limited to the question of jurisdiction over out-of-state defendants, we will not recount the extensive factual history of Ms. Hammons’ significant injuries, which is set forth in detail in the Superior Court decision, Hammons v. Ethicon, Inc., 190 A.3d 1248, 1254-58 (Pa. Super. 2018).

[J-2-2020] - 2 measured for width, courses, wales, thickness, areal density, and elasticity, and are then ball burst tested. These measurements are taken and recorded to ensure that Secant has knit the mesh per Ethicon’s specifications, and Secant completes a Certificate of Conformance for each lot that attests to the mesh’s compliance with Ethicon’s specifications. Secant then ships the large rolls of mesh to other Ethicon facilities unrelated to Secant where further manufacturing occurs. Affidavit of Karen West, dated June 2, 2014, at ¶ 5.

In May 2013, Hammons filed a complaint in the Philadelphia Court of Common

Pleas against Ethicon, Johnson & Johnson, Gynecare,2 and Secant, asserting various

claims related to the implanted device. Ethicon is a wholly-owned subsidiary of co-

defendant Johnson & Johnson, both of which are headquartered and incorporated in New

Jersey (jointly “Ethicon”).

After initially being removed to federal court based on Ethicon’s claim of diversity

jurisdiction, the case was eventually remanded to the Philadelphia Court of Common

Pleas, where it was transferred in March 2014 to the Complex Litigation Center Pelvic

Mesh Mass Tort Program, which has been coordinated under the caption In re Pelvic

Mesh Litigation and docketed as Master Docket Number February Term 2014, No. 829

(“Master Docket”).3 The Master Docket included plaintiffs who were residents of

2 Gynecare, initially named as a defendant, was a division of Ethicon.

3 The Superior Court summarized the history of Philadelphia’s mass tort program:

In 1992, the Philadelphia Court of Common Pleas initiated the Mass Tort Program to deal efficiently with large numbers of complex but similar tort cases by coordinating and streamlining pleadings, discovery, pretrial motions, and trial. The legal foundation for the Program is Pa.R.Civ.P. 213, which authorizes courts to consolidate related cases and issue case management orders for their efficient disposition.

Hammons, 190 A.3d at 1260.

[J-2-2020] - 3 Pennsylvania and over one hundred plaintiffs who, like Hammons, were neither residents

of Pennsylvania nor had the device implanted in Pennsylvania (jointly “Plaintiffs”).

On March 31, 2014, the court entered Case Management Order No. 1. In it, the

court set forth procedures for Plaintiffs to file a “Master Long Form Complaint” and

individual “Short Form Complaints.” It declared that the Master Complaint would

“substitute and supersede all [c]omplaints filed in individual Pelvic Mesh Cases pending

in the Philadelphia County Court of Common Pleas,” which included Hammons’

complaint. Order, dated March 31, 2014, at 3. The court decreed that the defendants

could file Master Preliminary Objections as well as a Master Answer in response to the

Master Complaint. The order specified that the court’s “ruling on the Master Preliminary

Objections will be binding on all current and future Pelvic Mesh Cases.” Id. at 3.

The case management order explained that, after the expiration of the deadlines

for Master Preliminary Objections, each plaintiff should file an individual Short Form

Complaint in a form proposed by the Plaintiffs and agreed to by the Defendants. Id. at 3-

4. On the Short Form Complaint, the individual plaintiffs could incorporate by reference

those counts of the Master Complaint that applied to them and raise any additional claims

specific to their situation. Any defendants named in a Short Form Complaint were allowed

to file preliminary objections relevant to the new issues raised in that individual complaint.

Plaintiffs filed the Master Complaint in May 2014 against ten defendants raising

eighteen claims. Plaintiffs asserted, without development, that jurisdiction over the

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