POLYFORM SYNTHETIC MESH
Report
- Report Number
- 3004859928-2013-00024
- Event Type
- Injury
- Date Received
- April 23, 2013
- Date of Event
- March 29, 2007
- Report Date
- April 22, 2013
- Manufacturer
- PROXY BIOMEDICAL LTD.
- Product Code
- FTL
- PMA / PMN Number
- K051245
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- NOT APPLICABLE
Narratives
THE DEVICE IS A SYNTHETIC DEVICE MADE FROM POLYPROPYLENE. INJURIES SUCH AS PAIN, MESH EROSION, INFECTION, INCONTINENCE, FISTULA FORMATION AND DYSPAREUNIA ARE DOCUMENTED RISKS ASSOCIATED WITH THE POLYFORM DEVICE - REFERENCE DESIGN FMEA AND POLYFORM PRODUCT INSERT (INSTRUCTIONS FOR USE).
PROXY BIOMEDICAL WAS NOTIFIED ON (B)(4) 2013 VIA EMAIL BY THE POLYFORM DISTRIBUTOR ((B)(4)) THAT THEY HAVE RECEIVED A COMPLAINT ON THE (B)(4) 2013 REGARDING A POLYFORM PRODUCT FROM A PATIENT'S LEGAL REPRESENTATIVE. THE COMPLAINT STATES THAT AS A RESULT OF THE POLYFORM IMPLANT (DATE OF IMPLANTATION IS ON (B)(6) 2007), A PATIENT INJURY OCCURRED. THE PATIENT IS IDENTIFIED AS "(B)(6)". HER DATE OF BIRTH IS UNKNOWN; HER WEIGHT AND HEIGHT DETAILS ARE UNKNOWN. THE HOSPITAL WHERE THE IMPLANTATION PROCEDURE TOOK PLACE IS THE (B)(6) USA. AN ADDITIONAL DEVICE WAS REPORTED TO HAVE BEEN IMPLANTED HOWEVER NO INFORMATION IS AVAILABLE REGARDING THIS DEVICE. THE PHYSICIAN WHO TREATED THE PATIENT IS DR (B)(6). THE POLYFORM PART NUMBER AND LOT NUMBER HAVE NOT BEEN PROVIDED. NO OTHER INFORMATION REGARDING THE PRODUCT OR THE PATIENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 173978 | POLYFORM SYNTHETIC MESH | MESH SURGICAL, POLYMERIC (FTL) | FTL | PROXY BIOMEDICAL LTD. | 840-240 OR 840-241 | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Other |