FDA Adverse Event
Injury
Summary report: N
PERIGEE MESH
MDR report key: 2932581
·
Received January 25, 2013
Report
- Report Number
- MW5028747
- Event Type
- Injury
- Date Received
- January 25, 2013
- Date of Event
- July 26, 2012
- Report Date
- January 14, 2013
- Manufacturer
- *
- Product Code
- OTP
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- MI, US
- Reporter Occupation
- PHYSICIAN ASSISTANT
Narratives
Description of Event or Problem · 1
PT HAD VAGINAL DISCHARGE, PAIN, URGENCY, AND RECURRENT UTIS BY ADVANTAGE FIT RETROPUBIC MIDURETERAL SLING, AND PERIGEE MESH.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 36200 | PERIGEE MESH | MESH | OTP | * | * | * | |
| 36201 | ADVANTAGE FIT | MIDURETHRAL SLING | FTL | * | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 60 YR | Hospitalization |