PELVISOFT ACELLULAR COLLAGEN BIOMESH
Report
- Report Number
- 1018233-2013-00487
- Event Type
- Injury
- Date Received
- February 21, 2013
- Report Date
- October 29, 2015
- Manufacturer
- TISSUE SCIENCE LABORATORIES
- Product Code
- FTM
- PMA / PMN Number
- K031332
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- ATTORNEY
- Health Professional
- N
Narratives
THE SAMPLE WAS NOT RETURNED. THE FINISHED PRODUCT MET ALL SPECIFICATIONS PRIOR TO BEING RELEASED FOR GENERAL DISTRIBUTION. THE INSTRUCTIONS FOR USE WHICH ACCOMPANIES ALL DEVICES CURRENTLY ADDRESSES POTENTIAL RISKS ASSOCIATED WITH SURGICALLY IMPLANTED MATERIALS. THE INSTRUCTIONS FOR USE STATE IN THE PRECAUTIONS: "PELVISOFT BIOMESH IS FOR SINGLE-PATIENT USE ONLY AND IS TO BE IMPLANTED SURGICALLY. IF EITHER THE OUTER POLYESTER/POLYETHYLENE POUCH OR THE INNER FOIL POUCH HAS BEEN PERFORATED OR TORN IN SHIPMENT OR STORAGE, THEN THE ENCLOSED PELVISOFT BIOMESH SHOULD NOT BE USED. PELVISOFT BIOMESH SHOULD BE HYDRATED OR MOIST WHEN THE PACKAGE IS OPENED. DEHYDRATED OR DRY TISSUE SHOULD NOT BE IMPLANTED." (B)(4).
THE PATIENT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADDITIONAL INFORMATION HAS BEEN REQUESTED, BUT NOT YET RECEIVED. ASSOCIATED MDR: 1018233-2013-00484, 1018233-2013-00485, 1018233-2013-00486,1018233-2013-00488, AND 1018233-2013-00489.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 75097 | PELVISOFT ACELLULAR COLLAGEN BIOMESH | Mesh, surgical | FTM | TISSUE SCIENCE LABORATORIES | NA | 07B02-1 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 64 YR | Female | Required Intervention | PELVILACE TO TRANSOBTURATOR BIOURETHRAL SUPPORT| PELVISOFT ACELLULAR COLLAGEN BIOMESH| SYSTEM| SYSTEM| PELVISOFT ACELLULAR COLLAGEN BIOMESH| PELVILACE TO TRANSOBTURATOR BIOURETHRAL SUPPORT |