FDA Adverse Event Injury Summary report: N

PELVICOL 2CM X 7CM 1.0MM

MDR report key: 3220989 · Received July 3, 2013

Report

Report Number
9617613-2013-00465
Event Type
Injury
Date Received
July 3, 2013
Date of Event
November 14, 2008
Report Date
June 10, 2013
Manufacturer
COVIDIEN, FORMERLY TISSUE
Product Code
FTL
PMA / PMN Number
K992556
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

PROCEDURE: UROGYNECOLOGICAL. ACCORDING TO THE REPORTER: THE PATIENT ALLEGED INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
305710 PELVICOL 2CM X 7CM 1.0MM PELVICOL MESH FTL COVIDIEN, FORMERLY TISSUE 08B01-9

Patients

Seq Age Sex Outcome Treatment
1 40 YR Female Other