FDA Adverse Event Injury Summary report: N

URETEX SUP URETHRAL SUPPORT SYSTEM

MDR report key: 3203738 · Received March 26, 2013

Report

Report Number
1018233-2013-00918
Event Type
Injury
Date Received
March 26, 2013
Report Date
February 25, 2013
Manufacturer
SOFRADIM PRODUCTION
Product Code
OTN
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
MO, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

THE PT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADDITIONAL INFO HAS BEEN REQUESTED, BUT NOT YET RECEIVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
125411 URETEX SUP URETHRAL SUPPORT SYSTEM OTN SOFRADIM PRODUCTION NA SGF00060

Patients

Seq Age Sex Outcome Treatment
1 44 YR Required Intervention