FDA Adverse Event Injury Summary report: N

MESH SLING

MDR report key: 3944463 · Received July 14, 2014

Report

Report Number
MW5037273
Event Type
Injury
Date Received
July 14, 2014
Date of Event
July 12, 2007
Report Date
July 13, 2014
Manufacturer
UNK
Product Code
OTN
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
OR, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

I HAVE A BLADDER MESH SLING FOR "UC". I HAVE EXTREME PAIN IN PELVIC AREA THAT DOCTORS WON'T HELP WITH. HAD THIS DONE IN 2007. HELP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
409905 MESH SLING MESH SLING OTN UNK

Patients

Seq Age Sex Outcome Treatment
1 41 YR Hospitalization