FDA Adverse Event
Injury
Summary report: N
URETEX TO URETHRAL SUPPORT SYSTEM
MDR report key: 3152142
·
Received May 23, 2013
Report
- Report Number
- 1018233-2013-02171
- Event Type
- Injury
- Date Received
- May 23, 2013
- Report Date
- April 23, 2013
- Manufacturer
- SOFRADIM PRODUCTION
- Product Code
- OTN
- Adverse Event
- Yes
- Report Source
- Distributor report
- Reporter Location
- NY, US
- Reporter Occupation
- ATTORNEY
Narratives
Description of Event or Problem · 1
COMPLAINT #(B)(4). IT WAS REPORTED BY THE PT'S ATTORNEY THAT AS A RESULT OF HAVING THE PRODUCT IMPLANTED, THE PT HAS EXPERIENCED PAIN, SUFFERING, DISABILITY AND IMPAIRMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 227814 | URETEX TO URETHRAL SUPPORT SYSTEM | OTN | SOFRADIM PRODUCTION | NA | SFI00533 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |