FDA Adverse Event Injury Summary report: N

PELVICOL ACELLULAR COLLAGEN MATRIC 4X7CM

MDR report key: 3131445 · Received May 10, 2013

Report

Report Number
9617613-2013-00230
Event Type
Injury
Date Received
May 10, 2013
Date of Event
February 9, 2004
Report Date
April 15, 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 PT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. PRODUCT WAS USED FOR THERAPEUTIC TREATMENT. SPARC SLING SYSTEM WITH TENSIONING SUTURE WAS REPORTED TO BE USED/IMPLANTED DURING THIS PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
209327 PELVICOL ACELLULAR COLLAGEN MATRIC 4X7CM PELVICOL MESH FTL COVIDIEN, FORMERLY TISSUE 03B14-B

Patients

Seq Age Sex Outcome Treatment
1 Other