FDA Adverse Event Injury Summary report: N

URETEX TO2 URETHRAL SUPPORT SYSTEM

MDR report key: 3221168 · Received May 22, 2013

Report

Report Number
1018233-2013-02151
Event Type
Injury
Date Received
May 22, 2013
Report Date
April 22, 2013
Manufacturer
SOFRADIM PRODUCTION
Product Code
OTN
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
CA, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

(B)(4). THE PATIENT'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
226831 URETEX TO2 URETHRAL SUPPORT SYSTEM OTN SOFRADIM PRODUCTION NA SFE00087

Patients

Seq Age Sex Outcome Treatment
1 43 YR Required Intervention