FDA Adverse Event Injury Summary report: N

PELVICOL ACELLULAR COLLAGEN MATRIX 4X7CM

MDR report key: 3014205 · Received March 5, 2013

Report

Report Number
9617613-2013-00076
Event Type
Injury
Date Received
March 5, 2013
Date of Event
February 2, 2007
Report Date
February 8, 2013
Manufacturer
COVIDIEN, FORMERLY TISSUE
Product Code
FTL
PMA / PMN Number
K992556
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

PROCEDURE TYPE: UROGYNECOLOGICAL. ACCORDING TO THE REPORTER: THE PATIENT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. PRODUCT WAS USED FOR THERAPEUTIC TREATMENT. ADDITIONAL INFORMATION FROM THE IMPORTER REPORT: ADDITIONAL INFORMATION HAS BEEN REQUESTED, BUT NOT YET RECEIVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
94920 PELVICOL ACELLULAR COLLAGEN MATRIX 4X7CM PELVICOL MESH FTL COVIDIEN, FORMERLY TISSUE NA 06B16-1

Patients

Seq Age Sex Outcome Treatment
1 Other| R