FDA Adverse Event
Malfunction
Summary report: N
CENTRA 850 BED
MDR report key: 1111973
·
Received August 12, 2008
Report
- Report Number
- 1824206-2008-03093
- Event Type
- Malfunction
- Date Received
- August 12, 2008
- Date of Event
- October 11, 2007
- Report Date
- October 11, 2007
- Manufacturer
- HILL-ROM RITTER
- Product Code
- FNL
- Report Source
- Manufacturer report
- Reporter Location
- MI, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE BRAKES NOT HOLDING COULD LEAD TO UNINTENTIONAL MOVEMENT OF THE BED WHICH HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN REPLACED THE CASTERS IN ORDER TO RESOLVE THE PROBLEM.
Description of Event or Problem · 1
THE BRAKES WOULD NOT HOLD ON THIS BED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CENTRA 850 BED | AC POWERED HOSPITAL BED | FNL | HILL-ROM RITTER | P850 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |