FDA Adverse Event
Other
Summary report: N
SYNTHES HEXAGONAL SCREWDRIVER
MDR report key: 55175
·
Received December 6, 1996
Report
- Report Number
- 2530088-1996-00006
- Event Type
- Other
- Date Received
- December 6, 1996
- Report Date
- December 5, 1996
- Manufacturer
- SYNTHES USA
- Product Code
- HXX
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AZ, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
TIP OF SCREWDRIVER BROKE INSIDE OF END CAP (IMPLANT SEE D-10), AND REMAINS IN PT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SYNTHES HEXAGONAL SCREWDRIVER | SCREWDRIVER | HXX | SYNTHES USA | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 26 YR | Other | END CAP (IMPLANT)-459.012 |