Moore v. Mount Sinai Hospital Medical Center of Chicago

2020 IL App (1st) 190321-U
Appellate Court of Illinois·Decided July 31, 2020·No. 1-19-0321·Unpublished·Cited by 1 cases

Opinion

2020 IL App (1st) 190321-U No. 1-19-0321

Order filed July 31, 2020 Fifth Division

NOTICE: This order was filed under Supreme Court Rule 23 and may not be cited as precedent by any party except in the limited circumstances allowed under Rule 23(e)(1).

IN THE

APPELLATE COURT OF ILLINOIS FIRST DISTRICT

TYRONE MOORE, )

) Appeal from the

Plaintiff-Appellant, ) Circuit Court of ) Cook County.

v. )

) No. 15 L 011893

MOUNT SINAI HOSPITAL MEDICAL CENTER OF ) CHICAGO, THE MOUNT SINAI COMMUNITY ) Honorable FOUNDATION d/b/a SINAI MEDICAL GROUP, SINAI ) Christopher R. Lawler, MEDICAL GROUP, LTD., STEPHEN R. WISE, M.D., ) Judge, Presiding. MEDTRONIC, INC., )

)

Defendants, )

)

(Medtronic, Inc., Defendant-Appellee). )

JUSTICE HALL delivered the judgment of the court.

Presiding Justice Hoffman and Justice Rochford concurred in the judgment.

ORDER

¶1 Held: Plaintiff’s product liability claim against defendant was time-barred by the two-

year statute of limitations which began to run when plaintiff knew or should have known that his injury was wrongfully caused.

¶2 Plaintiff, Tyrone Moore (Moore), appeals from an order of the circuit court which granted defendant, Medtronic, Inc.’s (Medtronic), motion to dismiss based upon the two-year statute of

limitations applicable to product liability claims. For the reasons that follow, we affirm the circuit court’s opinion.

¶3 BACKGROUND

¶4 In October of 2013, Moore sought medical treatment from Stephen Wise, M.D. for a possible repair of his ventral hernia. Upon examination, Dr. Wise diagnosed Moore with a reducible umbilical hernia and scheduled the hernia repair to take place at Mount Sinai Hospital Medical Center of Chicago (Mt. Sinai Hospital). On November 20, 2013, Moore underwent a laparoscopic ventral hernia repair of a six-by-six-centimeter hernia defect by Dr. Wise. Dr. Wise used a hernia mesh to repair Moore’s hernia which was manufactured and sold by Covidien at the time of Moore’s surgery. Covidien was subsequently purchased by Medtronic.

¶5 After discharge, Moore experienced vomiting, the inability to have a bowel movement and the inability to pass gas, which continued to worsen. On November 23, 2013, Moore contacted Dr. Wise who advised him to go to the emergency room and Dr. Wise would meet him. On December 1, 2013, Moore underwent a diagnostic laparoscopy by Dr. Wise which revealed that there was a small bowel mesentery incarcerated in a hole in the mesh that was used to repair Moore’s hernia.

¶6 On November 20, 2015, Moore filed his original complaint alleging medical malpractice against numerous healthcare providers, including Mt. Sinai Hospital, The Mount Sinai Community Foundation d/b/a Sinai Medical Group (Sinai Medical Group), and Dr. Wise, based upon his hernia repair surgery performed on November 20, 2013, and his subsequent care and treatment. The original complaint alleged that, “on December 1, 2013, the Plaintiff, TYRONE MOORE underwent a diagnostic laparascopy, which showed that there was small bowel mesentery incarcerated in a hole in the mesh that was used to repair the hernia.” It also alleged that, “during

the December 1, 2013, procedure, the mesentery and associated bowel were reduced. Supramesh was placed over the hole in the mesh and it was secured to the abdominal wall.”

¶7 On August 3, 2016, Moore filed his first amended complaint, in which he voluntarily dismissed all defendants, except Mt. Sinai Hospital and its associated entities and Dr. Wise. The complaint was accompanied by a report completed by a medical professional attesting to the merits of Moore’s medical malpractice allegations pursuant to section 2-622 of the Illinois Code of Civil Procedure (Code) (735 ILCS 5/2-622 (West 2016)). The author of the report was Christopher S. Pruett, M.D., a laparoscopic and general surgeon, and Moore’s retained expert. In his report, Dr. Pruett opined that he had reviewed Moore’s Mt. Sinai Hospital medical records and in his medical opinion, “[t]he discharge summary by Don Teed, M.D. documents that the stat CT scan on 11/23/13 revealed that there was a portion of small bowel mesentery possibly protruding through the mesh.” His report also indicated that, “[o]n 12/1/13 the patient underwent a diagnostic laparoscopy, reduction of small bowel mesentery from hole in mesh. Again, the surgery was performed by Stephen Wise, M.D. at Mount Sinai Medical Center and the surgical technique was dictated by resident surgeon Dahlia Tawfik-Sexton, M.D. The findings revealed small bowel mesentery incarcerated in 2X2 defect within mesh.” Dr. Pruett’s impression was that, “[t]he surgical technique utilized by Stephen Wise, M.D. and the attending doctors at Mount Sinai Medical Center, on 11/20/13, created a hole in the mesh designed to repair the ventral hernia, allowed the small bowel to incarcerate and constituted a deviation from the standard of care.”

¶8 The parties engaged in discovery, and on November 23, 2016, Dr. Wise filed his answers to Moore’s interrogatory requests. In his answers Dr. Wise stated that to the best of his knowledge, no inquiry, investigation, hearing or other procedure was conducted to obtain details of the events

set forth in Moore’s complaint, and directed Moore to his medical records in response to a request for a description of the nature and reason for his injuries.

¶9 On July 14, 2017, Dr. Wise was deposed. Dr. Wise testified that he did not believe that the hole in the mesh was caused by “anything that occurred intraoperatively because…I had an adequate look at the mesh up until the time of the termination of the procedure, and there was not a hole in it.” He testified that he had never used this mesh material previously and did not use it after Moore’s November 20, 2013, hernia surgery, “because of the problem [he] perceived with central mesh failure.”

¶ 10 On April 20, 2018, Dr. Tawfik-Sexton, Dr. Wise’s resident at the time of Moore’s surgery was deposed. She testified that she did not know how the hole in the mesh occurred and did not know possible causes for the hole in the mesh.

¶ 11 On May 1, 2018, Moore filed a second amended complaint, adding a product liability claim against Medtronic. Moore alleged that “on and prior to November 20, 2013,” Covidien “did design, manufacture, distribute, sell and/or place into the stream of commerce a certain hernia mesh product,” and that in January of 2015, Medtronic purchased Covidien. He also alleged that on November 20, 2013, Dr. Wise used the hernia mesh product during his surgery to repair his ventral hernia. Moore further alleged that, “the hernia mesh was not reasonably safe for its intended use, in that it could and did experience central mesh failure[;] * * * it was unreasonably dangerous[;] * * * and * * * proximately cause[d] [him] * * * to develop complications which led to multiple organ failure.”

¶ 12 On June 6, 2018, Medtronic filed a motion to dismiss pursuant to sections 2-619(a)(5) and 2-615 of the Code (735 ILCS 5/2- 615, 2-619(a)(5) (West 2018)), seeking dismissal of Moore’s

claim because it was time-barred by the two-year statute of limitations and that he failed to state a cause of action against it. 1

¶ 13 Medtronic argued that the statute of limitations for filing a product liability claim against it had expired on November 20, 2015, two years after Moore’s initial hernia surgery. It argued that Moore knew or had reason to know of his injury on November 20, 2013, at the earliest, or arguably, when he consulted an attorney to investigate any potential claims arising out of his hernia repair surgery in November of 2015, at the latest. Thus, when Moore filed his second amended complaint on May 1, 2018—nearly four-and-a-half years after the surgery at issue—naming Medtronic as a defendant, it was time-barred.

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Moore v. Mount Sinai Hospital Medical Center of Chicago, 2020 IL App (1st) 190321-U (Ill. Ct. App. 2020).

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