FDA Adverse Event
Malfunction
Summary report: N
P850 CENTRA BED
MDR report key: 1190650
·
Received October 3, 2008
Report
- Report Number
- 1824206-2008-03704
- Event Type
- Malfunction
- Date Received
- October 3, 2008
- Date of Event
- September 10, 2008
- Report Date
- September 10, 2008
- Manufacturer
- HILL-ROM RITTER.
- Product Code
- FNL
- Report Source
- Manufacturer report
- Reporter Location
- HI, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE HI-LOW DRIFTING IS UNINTENTIONAL MOVEMENT OF THE BED WHICH HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN CLEANED AND LUBRICATED THE HI-LOW DRIVE IN ORDER TO RESOLVE THE PROBLEM. ALL BED DRIVES ARE REQUIRED TO BE INSPECTED, CLEANED, AND LUBRICATED AT LEAST ONCE A YEAR IN ACCORDANCE WITH THE PRODUCT SERVICE MANUAL.
Description of Event or Problem · 1
A TECHNICIAN DISCOVERED THAT THIS BED WOULD DRIFT DOWN FROM THE UP POSITION. THERE WAS NO PATIENT IN THE BED AT THAT TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | P850 CENTRA BED | AC POWERED HOSPTIAL BED | FNL | HILL-ROM RITTER. | P850 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |