FDA Adverse Event Injury Summary report: N

PELVICOL 2X4 CM

MDR report key: 3231923 · Received July 11, 2013

Report

Report Number
9617613-2013-00487
Event Type
Injury
Date Received
July 11, 2013
Date of Event
February 18, 2002
Report Date
May 27, 2018
Manufacturer
COVIDIEN
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

TRACKING NUMBER: (B)(4).

Description of Event or Problem · 1

PROCEDURE: STRESS URINARY INCONTINENCE. ACCORDING TO THE REPORTER: THE PATIENT ALLEGED INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
321243 PELVICOL 2X4 CM PELVICOL MESH FTL COVIDIEN 01A06

Patients

Seq Age Sex Outcome Treatment
1 24 YR Female Other