FDA Adverse Event
Malfunction
Summary report: N
TRANSTAR STRETCHER
MDR report key: 1112087
·
Received August 6, 2008
Report
- Report Number
- 1824206-2008-03038
- Event Type
- Malfunction
- Date Received
- August 6, 2008
- Date of Event
- August 5, 2008
- Report Date
- August 5, 2008
- Manufacturer
- HILL-ROM RITTER
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- LA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE BRAKES NOT HOLDING/WORKING COULD LEAD TO UNINTENTIONAL MOVEMENT OF THE STRETCHER WHICH HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN REPLACED THE CASTERS AND HEX ROD IN ORDER TO RESOLVE THE PROBLEM.
Description of Event or Problem · 1
THE BRAKES ON THIS STRETCHER WOULD NOT OPERATE PROPERLY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TRANSTAR STRETCHER | WHEELED STRETCHER | FPO | HILL-ROM RITTER | P8000 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |