FDA Adverse Event
Malfunction
Summary report: N
CENTRA 850 BED
MDR report key: 1190634
·
Received October 3, 2008
Report
- Report Number
- 1824206-2008-03703
- 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
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WI, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
UPON COMPLAINT REVIEW, IT WAS DETERMINED THAT THE BRAKES NOT HOLDING/WORKING COULD LEAD TO UNINTENTIONAL MOVEMENT OF THE BED WHICH HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN ADJUSTED THE BRAKE CASTERS IN ORDER TO RESOLVE THE PROBLEM.
Description of Event or Problem · 1
THE BRAKES ON THIS BED WOULD NOT HOLD CORRECTLY.
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 |