FDA Adverse Event
Injury
Summary report: N
SLING WITH MESH
MDR report key: 3934335
·
Received July 10, 2014
Report
- Report Number
- MW5037239
- Event Type
- Injury
- Date Received
- July 10, 2014
- Date of Event
- May 16, 2014
- Report Date
- July 9, 2014
- Product Code
- OTN
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
PAIN AT LEVEL OF THE SLING WITH MESH EROSION AT THE MIDPORTION OF THE URETHRA, SHE DESIRED SURGICAL REMOVAL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 402520 | SLING WITH MESH | SLING WITH MESH | OTN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 29 YR | Hospitalization |