GRAPHIC CASE FOR VEPTR II ROD INSTRUMENTS
Report
- Report Number
- 3003787298-2013-10057
- Event Type
- Malfunction
- Date Received
- March 27, 2013
- Date of Event
- April 23, 2012
- Report Date
- April 23, 2012
- Manufacturer
- SYNTHES JENNERSVILLE
- Product Code
- LXH
- PMA / PMN Number
- EXEMPT
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- OTHER
Narratives
SYNTHES IS SUBMITTING THIS REPORT AS A RESULT OF REMEDIATION ACTIVITIES RELATED TO FDA WARNING LETTER DATED FEBRUARY 2012. DEVICE(S) LISTED IN THIS REPORT IS (ARE) USED FOR TREATMENT, NOT DIAGNOSIS. ANY ADDITIONAL INFORMATION RECEIVED REGARDING THIS EVENT AFTER FILING THIS REPORT SHALL BE FILED ON A SUPPLEMENTAL MDR. A REVIEW OF THE DEVICE HISTORY RECORDS WAS PERFORMED AND NO COMPLAINT RELATED ISSUES WERE FOUND. THE INVESTIGATION COULD NOT BE COMPLETED AND NO CONCLUSION COULD BE DRAWN AS NO PRODUCT WAS RECEIVED FOR EVALUATION. PLACEHOLDER.
SYNTHES IS SUBMITTING THIS REPORT AS A RESULT OF REMEDIATION ACTIVITIES RELATED TO FDA WARNING LETTER DATED FEBRUARY 2012. DEVICE(S) LISTED IN THIS REPORT IS (ARE) USED FOR TREATMENT, NOT DIAGNOSIS. ANY ADDITIONAL INFORMATION RECEIVED REGARDING THIS EVENT AFTER FILING THIS REPORT SHALL BE FILED ON A SUPPLEMENTAL MDR.
IT WAS REPORTED THAT THE CUSTOMER WAS CONCERNED THAT THE INSTRUMENTS IN THE VEPTR II GRAPHIC CASES COULD NOT BE PROPERLY STERILIZED BECAUSE THE PLASTIC COATING WAS PEELING OFF THE METAL. ACCOUNT WAS CONCERNED THAT DEBRIS COULD GET IN THE CREVICES BETWEEN THE PLASTIC AND METAL, CONTAMINATING THE INSTRUMENTS. THIS IS REPORT 5 OF 6 FOR THIS EVENT.
THIS IS REPORT 5 OF 6 FOR THIS COMPLAINT (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 125593 | GRAPHIC CASE FOR VEPTR II ROD INSTRUMENTS | LXH | SYNTHES JENNERSVILLE | 6451783 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |