FDA Adverse Event Injury Summary report: N

PELVICOL 6 X 8 CM

MDR report key: 3212788 · Received July 1, 2013

Report

Report Number
9617613-2013-00420
Event Type
Injury
Date Received
July 1, 2013
Date of Event
November 9, 2009
Report Date
June 10, 2013
Manufacturer
COVIDIEN, FORMERLY TISSUE SCIENCE
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 PT ALLEGED INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
299518 PELVICOL 6 X 8 CM PELVICOL MESH FTL COVIDIEN, FORMERLY TISSUE SCIENCE 08B04-1

Patients

Seq Age Sex Outcome Treatment
1 Female Other