FDA Adverse Event
Malfunction
Summary report: N
ATLAS
MDR report key: 1890428
·
Received October 27, 2010
Report
- Report Number
- 1831750-2010-03305
- Event Type
- Malfunction
- Date Received
- October 27, 2010
- Date of Event
- September 30, 2010
- Report Date
- September 30, 2010
- Manufacturer
- STRYKER CORP, MEDICAL DIVISION
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MI, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
IT IS REPORTED THAT THE FOWLER WOULD NOT GO UP. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ATLAS | HOSPITAL WHEELED STRETCHER | FPO | STRYKER CORP, MEDICAL DIVISION | 0660 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |