COMPOSIX MESH
Report
- Report Number
- 1213643-2008-00424
- Event Type
- Injury
- Date Received
- September 5, 2008
- Date of Event
- January 18, 2008
- Report Date
- August 6, 2008
- Manufacturer
- DAVOL INC., SUB. C.R. BARD, INC.
- Product Code
- FTL
- PMA / PMN Number
- K971745
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- RI, US
- Reporter Occupation
- ATTORNEY
Narratives
CURRENTLY, IT IS UNK WHETHER OR NOT THE DEVICE MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT AS NO PROD HAS BEEN RETURNED. WHILE RECURRENCE AND ADHESIONS ARE KNOWN ADVERSE EVENTS THAT ARE LISTED IN THE IFU, NO CONCLUSION CAN BE DRAWN AT THIS TIME. WE WILL SUBMIT A F/U REPORT WHEN/IF PROD IS RETURNED FOR EVAL OR ADD'L INFO BECOMES AVAILABLE. SEE MEDWATCH 1213643-2008-00425 FOR INFO RELATED TO THE OTHER MESH IMPLANTED IN 2002.
ATTY REPORTED: IN 2002 -- THE PT WAS IMPLANTED WITH TWO DAVOL COMPOSIX DUAL MESHES, TO REPAIR A POSTOPERATIVE VENTRAL HERNIA. AFTER IMPLANTATION, PT'S TRANSVERSE COLON ADHERED TO THE UPPER MIDLINE COMPOSIX MESH AND HERNIA DEFECTS RECURRED AROUND THE EDGES OF THE MESHES. IN 2007 -- PT'S ATTENDING SURGEON DECLINED TO EXPLANT THE ADHERENT MESH BECAUSE THE ADHESIONS WERE TOO GREAT TO EXCISE, FOR FEAR OF OPENING THE COLON. INSTEAD OF EXPLANTING, THE SURGEON WAS FORCED TO INSERT TWO ADD'L PROLENE MESHES TO COMPENSATED FOR THE FAILURE OF THE COMPOSIX MESHES. ON THE PT'S INFO AND BELIEF, THE COMPOSIX MESHES "DELAMINATED AND/OR HARDENED CAUSING ADHESIONS TO THE COLON AND CAUSING RECURRENT HERNIAS".
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | COMPOSIX MESH | FTL | DAVOL INC., SUB. C.R. BARD, INC. | NA | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |