FDA Adverse Event
Malfunction
Summary report: N
ELECTRIC STRETCHER 12/09
MDR report key: 2925622
·
Received January 22, 2013
Report
- Report Number
- 0001831750-2013-00279
- Event Type
- Malfunction
- Date Received
- January 22, 2013
- Date of Event
- January 3, 2013
- Report Date
- January 3, 2013
- Manufacturer
- STRYKER MEDICAL-KALAMAZOO
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD END JACK COULD NOT BE PUMPED UP.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 31086 | ELECTRIC STRETCHER 12/09 | STRETCHER, WHEELED | FPO | STRYKER MEDICAL-KALAMAZOO | 1550 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |