FDA Adverse Event Injury Summary report: N

URETEX SUP URETHRAL SUPPORT SYSTEM

MDR report key: 3172325 · Received April 12, 2013

Report

Report Number
1018233-2013-01301
Event Type
Injury
Date Received
April 12, 2013
Report Date
March 13, 2013
Manufacturer
SOFRADIM PRODUCTIONS
Product Code
OTN
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
FL, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

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

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
159830 URETEX SUP URETHRAL SUPPORT SYSTEM OTN SOFRADIM PRODUCTIONS NA SGJ00478

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention