FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE BED
MDR report key: 2843603
·
Received October 24, 2012
Report
- Report Number
- 1824206-2012-06802
- Event Type
- Malfunction
- Date Received
- October 24, 2012
- Date of Event
- October 5, 2012
- Report Date
- October 5, 2012
- Manufacturer
- HILL-ROM INC
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NC, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN FOUND THE BATTERY WAS WEAK AND WOULD FAIL ONCE A FUNCTION WAS ACTIVATED AND THE BATTERY DID NOT RETAIN A CHARGE. THE TECHNICIAN REPLACED THE BATTERY TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
THE TECHNICIAN ALLEGED THAT WHEN THE BED WAS UNPLUGGED THE BATTERY LIGHT WAS ILLUMINATED. THE LIGHT WOULD GO OUT AFTER A SHORT PERIOD OF TIME OR IF A FUNCTION ACTIVATED. NO INJURY REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE BED | A/C POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM INC | 1900 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |