FDA Adverse Event Injury Summary report: N

URETEX TO2 URETHRAL SUPPORT SYSTEM

MDR report key: 3221121 · Received May 10, 2013

Report

Report Number
1018233-2013-01884
Event Type
Injury
Date Received
May 10, 2013
Report Date
April 10, 2013
Manufacturer
SOFRADIM PRODUCTION
Product Code
OTN
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
TX, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

THE PT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. PER ADD'L INFO RECEIVED, THE PT HAS EXPERIENCED LYSIS OF ADHESIONS, AND UTEROSACRAL LIGAMENT SUSPENSION, TOTAL LAPAROSCOPIC HYSTERECTOMY, BILATERAL SALPINGO-OOPHORECTOMY, TRANSOBTURATOR TAPE PLACEMENT, CYSTOSCOPY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
209457 URETEX TO2 URETHRAL SUPPORT SYSTEM OTN SOFRADIM PRODUCTION NA SGI00088

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention