SMALL HEXAGONAL SCREWDRIVER LONG
Report
- Report Number
- 8030965-2013-02188
- Event Type
- Malfunction
- Date Received
- May 15, 2013
- Date of Event
- April 16, 2013
- Report Date
- April 16, 2013
- Manufacturer
- SYNTHES GMBH
- Product Code
- HXX
- PMA / PMN Number
- EXEMPT
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IA
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. DEVICE IS AN INSTRUMENT AND IS NOT IMPLANTED/EXPLANTED. A PRODUCT DEVELOPMENT EVENT EVALUATION WAS CONDUCTED AND THE REPORT INDICATES THE RETURNED SMALL HEXAGONAL SCREWDRIVER LONG WAS MANUFACTURED IN DECEMBER 2010 AND IS OVER 2 YEARS OLD. THE SHAFT COMPONENT WAS MANUFACTURED FROM (B)(4), WHICH IS A TYPICAL MATERIAL USED TO MAKE HEXAGONAL SCREWDRIVER SHAFTS. THE DESIGN IS ADEQUATE FOR ITS INTENDED USE AND DID NOT CONTRIBUTE TO THIS COMPLAINT CONDITION. THE RETURNED SCREW WAS MANUFACTURED FROM (B)(4), WHICH IS A TYPICAL MATERIAL USED TO MAKE IMPLANT SCREWS. THE LOW PROFILE PELVIC PLATE SYSTEM RISK ANALYSIS ADEQUATELY ASSESSES THE RISK ASSOCIATED WITH THIS COMPLAINT CONDITION. THE SCREW WAS RETURNED WITH FRACTURED THREADED TIP, THE TIP FRAGMENT WAS NOT RETURNED FOR EVALUATION. THE SCREW SHAFT IS BENT AND THE SCREW HEAD IS NO LONGER PERPENDICULAR THE SHAFT. THE BENT SCREW INFERS THAT AN OFF AXIS FORCE WAS APPLIED DURING INSERTION CAUSING THE SCREW TO BEND AND BREAK AND ULTIMATELY CAUSING THE SCREWDRIVER TIP TO BREAK. THE MANUFACTURING DOCUMENTS WERE REVIEWED AND NO COMPLAINT RELATED ISSUES WERE FOUND.
THE SALES CONSULTANT REPORTED AN ISSUE WITH THE SCREWDRIVER THAT OCCURRED DURING OPEN REDUCTION INTERNAL FIXATION SURGERY (ORIF) OF TIBIA. THE SCREWDRIVER BROKE OFF IN THE HEAD OF THE SCREW ON (B)(6) 2013. CONCURRENTLY, THE HEAD OF THE SCREW AND APPROXIMATELY 1/2 OF THE SCREW SHAFT ALSO BROKE OFF DURING SURGERY. THE BALANCE OF THE SCREW SHAFT REMAINS IMPLANTED. THE SURGEON COMPLETED THE PROCEDURE WITH NO FURTHER PROBLEM. THE TIP OF THE DRIVER WAS DISCARDED BY THE FACILITY. THIS IS 2 OF 2 DEVICES FOR THIS EVENT REPORTED ON (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 215373 | SMALL HEXAGONAL SCREWDRIVER LONG | HXX | SYNTHES GMBH | 3577727 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 34 YR |