FDA Adverse Event Injury Summary report: N

C-QIR V-PATCH

MDR report key: 11234021 · Received January 26, 2021

Report

Report Number
3011175548-2021-00085
Event Type
Injury
Date Received
January 26, 2021
Report Date
January 26, 2021
Manufacturer
ATRIUM MEDICAL CORPORATION
Product Code
FTL
PMA / PMN Number
K090909
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 0

PLAINTIFF ALSO ALLEGEDLY EXPERIENCED ADHESIONS AND INCARCERATION. NOTE: MESH WAS SOAKED IN BACITRACIN SALINE SOLUTION OFF LABEL.

Additional Manufacturer Narrative · 1

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.

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 RECURRENT HERNIA, CHRONIC PAIN, INFLAMMATION AND FOREIGN BODY, GIANT CELL REACTION AND ADDITIONAL SURGERY. 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
129243 C-QIR V-PATCH MESH, SURGICAL, POLYMERIC FTL ATRIUM MEDICAL CORPORATION

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention