FDA Adverse Event
Malfunction
Summary report: N
THOR MONOLITHIC SCREWDRIVER SHAFT
MDR report key: 2801286
·
Received October 17, 2012
Report
- Report Number
- 9617544-2012-00445
- Event Type
- Malfunction
- Date Received
- October 17, 2012
- Date of Event
- September 20, 2012
- Report Date
- September 20, 2012
- Manufacturer
- STRYKER SPINE BORDEAUX
- Product Code
- HXX
- PMA / PMN Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
ADDITIONAL INFORMATION HAS BEEN REQUESTED AND IF MADE AVAILABLE WILL BE REPORTED IN A SUPPLEMENTAL. METHOD, RESULT, AND CONCLUSION CODES WILL BE MADE AVAILABLE FOLLOWING AN ENGINEERING EVALUATION.
Description of Event or Problem · 1
IT WAS REPORTED THAT, "DR PUTTING IN SCREW, THE SCREWDRIVER STRIPPED THE SCREW. HE THEN TRIED THE UNIVERSAL SCREWDRIVER, ITS STRIPPED AND SPLIT IN HALF. THEY THEN BROUGHT IN A UNIVERSAL SCREW REMOVAL SET TO TRY AND FINISH LOCKING THE SCREW BUT COULD NOT FIAL TIGHTEN OR REMOVE 2 SCREWS."
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | THOR MONOLITHIC SCREWDRIVER SHAFT | INSTRUMENT | HXX | STRYKER SPINE BORDEAUX | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |