FDA Adverse Event
Malfunction
Summary report: N
VERSACARE BED
MDR report key: 2842694
·
Received November 13, 2012
Report
- Report Number
- 1824206-2012-07343
- Event Type
- Malfunction
- Date Received
- November 13, 2012
- Date of Event
- October 22, 2012
- Report Date
- October 22, 2012
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN REPLACED THE COILED CABLE TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
THE TECHNICIAN ALLEGED THAT THE BED IS NOT INFLATING AND THE BRAKE CASTER RUBBED THE INSULATION FROM THE COILED CABLE AND BARE WIRES ARE SHOWING. NO PT IMPACT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VERSACARE BED | A/C POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM, INC. | 3200 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |