FDA Adverse Event Injury Summary report: N

URETEX TO URETHRAL SUPPORT SYSTEM

MDR report key: 3213444 · Received April 5, 2013

Report

Report Number
1018233-2013-01191
Event Type
Injury
Date Received
April 5, 2013
Report Date
March 6, 2013
Manufacturer
SOFRADIM PRODUCTION
Product Code
OTN
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
GA, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

THE PT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADD'L INFO HAS BEEN REQUESTED, BUT NOT YET REC'D.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
142319 URETEX TO URETHRAL SUPPORT SYSTEM OTN SOFRADIM PRODUCTION NA SFBC0019

Patients

Seq Age Sex Outcome Treatment
1 63 YR Required Intervention