FDA Adverse Event
Other
Summary report: N
STRYKER 5.5MM BARREL BUR, 12 FLUTE
MDR report key: 371085
·
Received January 7, 2002
Report
- Report Number
- 2648666-2001-00045
- Event Type
- Other
- Date Received
- January 7, 2002
- Date of Event
- December 6, 2001
- Report Date
- January 4, 2002
- Manufacturer
- STRYKER ENDOSCOPY
- Product Code
- HRX
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
IT WAS ALLEGED THAT THE HUB OVERHEATED CAUSING A BURN TO THE PT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | STRYKER 5.5MM BARREL BUR, 12 FLUTE | SHAVER BLADE | HRX | STRYKER ENDOSCOPY | 0275-951-012 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |