FDA Adverse Event Death Summary report: N

C-QUR TACSHIELD

MDR report key: 8845992 · Received July 31, 2019

Report

Report Number
3011175548-2019-00823
Event Type
Death
Date Received
July 31, 2019
Report Date
July 31, 2019
Manufacturer
ATRIUM MEDICAL CORPORATION
Product Code
FTL
PMA / PMN Number
K100076
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WI
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

BASED ON THE REVIEW OF THE DEVICE HISTORY RECORDS AND PRODUCT COMPLAINT DETAILS ATRIUM CAN FIND NO FAULT WITH THE PRODUCT. THIS LOT OF MESH PASSED ALL QUALITY AND PERFORMANCE REQUIREMENTS.

Description of Event or Problem · 0

PLAINTIFF ALSO ALLEGEDLY EXPERIENCED ADHESIONS, MESHOMA, SMALL BOWEL REPAIR, EDEMA, DEBRIDEMENT, DRAINAGE, 2XVAC FOLLOWED BY ABDOMINAL BINDER.

Additional Manufacturer Narrative · 1

WE ARE UNABLE TO FULLY INVESTIGATE THIS EVENT AS NO PRODUCT CODE, LOT NUMBER, OR SAMPLE WAS PROVIDED. NOT RETURNED.

Description of Event or Problem · 1

THIS EVENT IS DEEMED REPORTABLE BASED ON THE ALLEGATIONS IN A LAWSUIT WHICH, WHILE UNSUBSTANTIATED, SUGGEST THAT A REPORTABLE EVENT MAY HAVE OCCURRED DURING USE OF ATRIUM MEDICAL¿S MESH PRODUCT. PLAINTIFF ALLEGEDLY EXPERIENCED ABDOMINAL PAIN, INFECTION, ABSCESS, CELLULITIS, RECURRENT PANNICULITIS, ANOXIC ENCEPHALOPATHY, AND DEATH. SINCE THIS IS A LEGAL MATTER, THE CASE HAS BEEN TURNED OVER TO LEGAL COUNSEL AND FURTHER INFORMATION OBTAINED THROUGH INVESTIGATION OR DISCOVERY MAY FALL UNDER THE ATTORNEY/CLIENT AND/OR WORK PRODUCT PRIVILEGE. HOWEVER, ATRIUM WILL SUPPLEMENT THIS REPORT AS APPROPRIATE IF ADDITIONAL INFORMATION COMES TO ITS ATTENTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
640647 C-QUR TACSHIELD MESH, SURGICAL, POLYMERIC FTL ATRIUM MEDICAL CORPORATION 31644 10707219

Patients

Seq Age Sex Outcome Treatment
1 Death| R