FDA Adverse Event Injury Summary report: N

PELVICOL 6 X 8 CM

MDR report key: 3131395 · Received May 13, 2013

Report

Report Number
9617613-2013-00227
Event Type
Injury
Date Received
May 13, 2013
Date of Event
January 3, 2008
Report Date
April 15, 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

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

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

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
211892 PELVICOL 6 X 8 CM PELVICOL MESH FTL COVIDIEN, FORMERLY TISSUE SCIENCE 06B14-9

Patients

Seq Age Sex Outcome Treatment
1 74 YR