FDA Adverse Event
Malfunction
Summary report: N
SM204 M-SERIES W/BIG WHEEL
MDR report key: 1853044
·
Received September 21, 2010
Report
- Report Number
- 1831750-2010-02469
- Event Type
- Malfunction
- Date Received
- September 21, 2010
- Date of Event
- August 24, 2010
- Report Date
- August 24, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIV
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IN, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
GAS SPRING TRIP.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE FOWLER CANNOT BE RAISED USING THE YELLOW ACTIVATION HANDLES. THERE WAS NO PT INVOLVEMENT. NO ADVERSE CONSEQUENCES WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SM204 M-SERIES W/BIG WHEEL | HOSPITAL WHEELED STRETCHER | FPO | STRYKER CORP., MEDICAL DIV | 1015 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |