PDS LL PLUS ANTIBACTERIAL SUTURE
Report
- Report Number
- 2210968-2012-07046
- Event Type
- Injury
- Date Received
- November 6, 2012
- Report Date
- October 9, 2012
- Manufacturer
- ETHICON, INC.
- Product Code
- NEW
- PMA / PMN Number
- K061037
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AS
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4). CONCLUSION: THE PRODUCT UPON WHICH THIS MEDWATCH IS BASED IS ANTICIPATED. ONCE THE PRODUCT IS RECEIVED, ANY FURTHER INFORMATION DERIVED FROM THE EVALUATION WILL BE SUBMITTED IN A SUPPLEMENTAL 3500A FORM. THE ACTUAL DEVICE BATCH NUMBER ASSOCIATED WITH THIS EVENT IS NOT KNOWN. THE INTERNATIONAL AFFILIATE REPORTS THE FOLLOWING POSSIBLE BATCH NUMBERS: (B)(4) - LOT DK2267, (B)(4) - LOT EE2039, (B)(4).
(B)(4) - THE SURGEON OPINES THAT THE PATIENT DEVELOPED TISSUE NECROSIS AT THE SUBCUTANEOUS LAYER APPROXIMATELY EIGHT WEEKS POST OPERATIVE WHICH DEVELOPED INTO A SECONDARY (B)(6) INFECTION.(B)(4).
(B)(4). IN ADDITION, A REVIEW OF THE BATCH MANUFACTURING RECORDS FOR THE POSSIBLE BATCH NUMBERS WAS CONDUCTED AND THE BATCHES MET ALL FINISHED GOODS RELEASE CRITERIA. REPRESENTATIVE SAMPLES WERE RETURNED FOR EVALUATION. THEY WERE VISUALLY AND FUNCTIONALLY EVALUATED AND THEY MET THE REQUIREMENTS.
IT WAS REPORTED THAT A PATIENT UNDERWENT AN UNKNOWN PROCEDURE ON AN UNKNOWN DATE AND SUTURE WAS USED. THE PATIENT DEVELOPED AN INFECTION APPROXIMATELY SIX WEEKS POST OPERATIVE. THE WOUND WAS POSITIVE FOR A STAPH INFECTION. THE PATIENT WAS TREATED WITH CEPHALEX. ADDITIONAL INFORMATION HAS BEEN REQUESTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PDS LL PLUS ANTIBACTERIAL SUTURE | SUTURE, ABSORBABLE | NEW | ETHICON, INC. | NA | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |