FDA Adverse Event Injury Summary report: N

URETEX TO URETHRAL SUPPORT SYSTEM

MDR report key: 3142353 · Received May 15, 2013

Report

Report Number
1018233-2013-01970
Event Type
Injury
Date Received
May 15, 2013
Report Date
April 15, 2013
Manufacturer
SOFRADIM PRODUCTION
Product Code
OTN
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
IL, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

(B)(4). THE PT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADD'L INFO HAS BEEN REQUESTED, BUT NOT YET RECEIVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
215961 URETEX TO URETHRAL SUPPORT SYSTEM OTN SOFRADIM PRODUCTION NA UNK

Patients

Seq Age Sex Outcome Treatment
1 43 YR Required Intervention