STEVE TABOR VS. JOHNSON & JOHNSON (L-0830-14, ATLANTIC COUNTY AND STATEWIDE)

New Jersey Superior Court Appellate Division·Decided December 24, 2019·No. A-4703-17T1·Unpublished

Opinion

NOT FOR PUBLICATION WITHOUT THE APPROVAL OF THE APPELLATE DIVISION This opinion shall not "constitute precedent or be binding upon any court." Although it is posted on the internet, this opinion is binding only on the parties in the case and its use in other cases is limited. R. 1:36-3.

SUPERIOR COURT OF NEW JERSEY APPELLATE DIVISION

DOCKET NO. A-4703-17T1

STEVE TABOR and STACY SCROGGINS, h/w,

Plaintiffs-Appellants,

v.

JOHNSON & JOHNSON and ETHICON, INC.,

Defendants-Respondents.

Argued October 18, 2019 – Decided December 24, 2019 Before Judges Ostrer and Vernoia.

On appeal from the Superior Court of New Jersey, Law Division, Atlantic County, Docket No. L-0830-14.

Shay S. Deshpande argued the cause for appellants (Franzblau Dratch, attorneys; Shay S. Deshpande, on the brief).

David R. Kott argued the cause for respondents (Riker Danzig Scherer Hyland & Perretti, LLP, and Mc Carter & English, LLP, attorneys for respondents; David R.

Kott and Kelly Strange Crawford, of counsel; Jean Paige Patterson, on the brief).

PER CURIAM In this products liability action, plaintiffs Steve Tabor and his wife, Stacy Scroggins, appeal from orders granting summary judgment to defendants Johnson & Johnson and Ethicon, Inc. (Ethicon), dismissing the complaint on statute of limitations grounds, and denying plaintiffs' cross-motion to extend discovery and compel the deposition of a Johnson & Johnson corporate representative. We affirm in part, reverse in part, vacate in part, and remand for further proceedings.

I.

On February 28, 2014, plaintiffs filed a complaint against defendants alleging that more than three years earlier, on January 6, 2011, "Tabor had a heavy duty polypropylene . . . mesh," manufactured by defendants, "implanted surgically to repair a left inguinal hernia." The complaint further averred that following the surgery, Tabor suffered injuries and pain and suffering due to defects in the mesh. Plaintiffs asserted causes of action under the Product Liability Act (the Act), N.J.S.A. 2A:58C-1 to -11, (counts one and two); common law claims for strict liability (count three); defective design (count four); negligence (count five); breach of express warranty (count six); and a claim defendants violated the New Jersey Consumer Fraud Act (CFA), N.J.S.A.

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56:8-1 to -91, (count seven). Scroggins also asserted a cause of action for loss of consortium (count eight).

In February 2018, following the close of fact discovery, defendants moved for summary judgment, asserting plaintiffs' causes of action under the Act; the CFA; and for strict liability, defective design, and negligence were barred by the two-year statute of limitations for personal injury claims. See N.J.S.A. 2A:14- 2(a). Defendants argued plaintiffs had reason to know about those claims by as early as May 2011, were required to file the claims by no later than May 2013, and untimely filed the claims in February 2014.

The record is unclear as to the basis for defendants' motion for summary judgment on the breach of express warranty claim because, as defendants acknowledge, the breach of express warranty claim is subject to a four-year limitations period. Thus, even assuming plaintiffs were aware of the alleged breach of express warranty claim in May 2011, the February 2014 complaint was filed within the limitations period applicable to that claim.1

1 Defendants' notice of motion was labeled as one seeking summary judgment and dismissal for failure to state a claim, but the body of the notice refers only to the summary judgment rule, R. 4:46, and makes no reference to Rule 4:6-2(e), which governs motions to dismiss for failure to state a claim upon which relief may be granted.

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Plaintiffs filed opposition to the summary judgment motion and a cross-

motion to extend discovery and compel the deposition of a Johnson & Johnson corporate representative. The court heard argument on the motions and ordered a Lopez2 hearing to determine when plaintiffs' causes of action accrued. The court also determined that resolution of plaintiffs' cross-motion should abide the outcome of the Lopez hearing. The Lopez Hearing Tabor was the only witness presented during the Lopez hearing. He testified he had been employed as a truck driver, his highest level of education was the tenth grade, and he underwent a left inguinal hernia surgery in January 2011 after suffering an injury at work. Dr. Tommy Dinh performed the surgery. Prior to the surgery, Tabor signed a written authorization for a "left inguinal repair with mesh" procedure. The notice included a warning that potential complications included "serious injury or death."

Immediately following the surgery and during the ensuing months, Tabor suffered from severe pain in his groin area and left testicle, and numbing of his legs and lower back. Approximately seven weeks after the procedure, on February 24, 2011, he met with Dr. Dinh for a post-surgical follow-up visit. At

2 Lopez v. Swyer, 62 N.J. 267 (1973).

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that time, Tabor did not believe the constant and, at times, severe and unbearable pain he continued to experience was related to the "incisional pain at the site of [his] surgical incision." He testified the pain felt "like someone ha[d] kicked [him] in the groin [twenty-four] hours a day." In February 2011, Tabor began to "wonder" if the surgeon "had done something wrong," and if there was "something wrong" with the mesh. During a March 21, 2011 consultation with Dr. Dinh, Tabor "inferred" that Dr. Dinh opined that Tabor "had possible neuropathy of the inguinal nerve."

Tabor obtained the medical records concerning his surgery from the facility where the procedure was performed and learned the mesh was manufactured by Ethicon. On May 18, 2011, Tabor called Ethicon, spoke to a representative, and "reported experiencing pain and infection one month after a prolene hernia mesh procedure" and "felt something didn't belong there." Tabor also reported that his physician "prescribed antibiotics for infection," and that he felt he was "rejecting the implanted mesh." During the Lopez hearing, Tabor was shown a May 19, 2011 letter from Ethicon to him, describing the report he made to the representative, and he testified that he "believe[d]" and "assum[ed]" he produced the letter during discovery.

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Tabor also testified about a June 13, 2011 letter from Ethicon to him that reiterated the May 2011 letter's summary of his conversation with the representative and noted that the May 2011 letter "request[ed] additional information and . . . permission to contact [Tabor's] physician regarding [Tabor's] condition." The June 2011 letter further stated that Ethicon had "attempted to contact [Tabor] via telephone." Tabor testified he did not provide the requested information or permission to contact his physicians "because [he] didn't know what was wrong and [he is] not a doctor."

Tabor testified that one month later, on July 22, 2011, he met with a surgeon, Dr. Ancel Rogers, who told him "that one of the possible causes of [his] pain is irritation of nerves and or surrounding tissues from the implementation of prolene mesh."3 During the following months, Tabor met with other healthcare providers concerning his ongoing pain. During his testimony, Tabor agreed that on January 6, 2012, he met with Dr. Rogers, and that Dr. Rogers's medical records from the visit state that Dr. Rogers recommended Tabor undergo a CT scan "to verify whether or not he has a recurrent hernia or some mal-positioning of the

3 In the record, Dr. Rogers' first name is listed variously as "Ansell" and "Ancel." We employ "Ancel" because it is the name used by the trial court in its written decision.

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implanted mesh." Tabor, however, testified he could not recall if Dr. Rogers communicated that recommendation to him during the January 6, 2012 visit.

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