SMALL HOHMANN RETRACTOR 8MM SHORT NARROW TIP 160MM
Report
- Report Number
- 8030965-2013-10550
- Event Type
- Malfunction
- Date Received
- March 20, 2013
- Report Date
- February 6, 2012
- Manufacturer
- SYNTHES GMBH
- Product Code
- GAD
- PMA / PMN Number
- EXEMPT
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
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. THE DEVICE HISTORY RECORD WAS NOT AVAILABLE AS INSTRUMENT IS NEARLY 10 YEARS OLD. THE WHOLE INSTRUMENT IS DISCOLORED. THE RETRACTOR CORRESPONDS TO THE DRAWING AND PROCESSES AT THE TIME OF MANUFACTURE. THE RETRACTOR WAS NOT CLEANED PROPERLY.
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. ACTUAL EVENT DATE IS UNKNOWN. THIS IS REPORT 3 OF 6 FOR COMPLAINT (B)(4). ORIGINAL AWARENESS DATE IS (B)(6) 2012. PLACEHOLDER.
ACCOUNT COMPLAINED TO THE SALES CONSULTANT THAT THE INSTRUMENTS ARE RUSTING AROUND THE ETCH. THIS IS 3 OF 6 REPORTS FOR THE SAME EVENT.
THIS IS REPORT 3 OF 6 FOR COMPLAINT (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 116494 | SMALL HOHMANN RETRACTOR 8MM SHORT NARROW TIP 160MM | GAD | SYNTHES GMBH | A7 LA 26 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |