FDA Adverse Event Death Summary report: N

C-QUR MESH

MDR report key: 17347715 · Received July 18, 2023

Report

Report Number
3011175548-2023-00152
Event Type
Death
Date Received
July 18, 2023
Report Date
July 17, 2023
Manufacturer
ATRIUM MEDICAL CORPORATION
Product Code
FTL
PMA / PMN Number
K050311
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

WE ARE UNABLE TO FULLY INVESTIGATE THIS EVENT AS NO PRODUCT CODE, LOT NUMBER, OR SAMPLE WAS PROVIDED. THIS REPORT IS BASED UPON ALLEGATIONS MADE IN A LAWSUIT IN WHICH ATRIUM MEDICAL IS NAMED AS A DEFENDANT. THIS REPORT SHALL NOT BE CONSIDERED AS AN ADMISSION BY ATRIUM MEDICAL THAT THE PRODUCT DESCRIBED IN THE LAWSUIT CLAIM AND DESCRIBED HEREIN IS OR WAS DEFECTIVE, OR THAT IT HAD ANY CAUSAL RELATIONSHIP TO ANY INJURIES ALLEGEDLY SUFFERED BY THE PLAINTIFF. H3 OTHER TEXT : NOT RETURNED.

Description of Event or Problem · 0

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 RECURRENT INCARCERATED VENTRAL HERNIA AND ADHESIONS REQUIRING REPAIR, DURING REPAIR PLAINTIFF SUFFERED A CARDIAC EVENT AND AS PRONOUNCED DECEASED IN THE OPERATIVE ROOM. 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
41792 C-QUR MESH MESH, SURGICAL, POLYMERIC FTL ATRIUM MEDICAL CORPORATION

Patients

Seq Age Sex Outcome Treatment
1 Female Death