POLYFORM SYNTHETIC MESH
Report
- Report Number
- 3004859928-2013-00043
- Event Type
- Injury
- Date Received
- May 28, 2013
- Date of Event
- February 20, 2007
- Report Date
- May 13, 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
DEVICE WAS NOT RETURNED FOR EVAL. 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)(6) 2013 VIA EMAIL BY THE POLYFORM DISTRIBUTOR (BOSTON SCIENTIFIC) THAT THEY HAVE RECEIVED A COMPLAINT ON THE (B)(6) 2013 REGARDING A POLYFORM PRODUCT FROM A PT'S LEGAL REP. THE COMPLAINT STATES THAT AS A RESULT OF THE POLYFORM IMPLANT (DATE OF IMPLANTATION IS (B)(6) 2007), A PT INJURY OCCURRED. THE PT IS IDENTIFIED AS "(B)(6)". HER DATE OF BIRTH IS UNK; HER WEIGHT AND HEIGHT DETAILS ARE UNK. THE HOSPITAL WHERE THE IMPLANTATION PROCEDURE TOOK PLACE IS (B)(6). THE PHYSICIAN WHO TREATED THE PT IS UNK; BOTH DR (B)(6) WERE LISTED IN THE COMPLAINT, HOWEVER IT IS UNK WHICH PHYSICIAN PERFORMED THE PROCEDURE. THE POLYFORM PART NUMBER AND LOT NUMBER HAVE NOT BEEN PROVIDED. NO OTHER INFO REGARDING THE PRODUCT OR THE PT IS AVAILABLE AT THIS TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 232990 | POLYFORM SYNTHETIC MESH | MESH SURGICAL, POLYMERIC (FTL) | FTL | PROXY BIOMEDICAL LTD. | 10X15CM OR 15X20CM | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK | Other |