FDA Adverse Event
Malfunction
Summary report: N
CENTRA BED
MDR report key: 1954040
·
Received December 16, 2010
Report
- Report Number
- 1824206-2010-11640
- Event Type
- Malfunction
- Date Received
- December 16, 2010
- Date of Event
- November 29, 2010
- Report Date
- November 29, 2010
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECH FOUND THE BED EXIT TAPE SWITCH IS THE CAUSE OF THE BED EXIT NOT ALARMING. TECH REPLACED THE TAPE SWITCH TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
TECH ALLEGED THAT THE BED EXIT IS NOT ALARMING. NO PT IMPACT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CENTRA BED | A/C POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM, INC. | 850 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |