FDA Adverse Event
Malfunction
Summary report: N
VERSACARE BED
MDR report key: 2974642
·
Received January 29, 2013
Report
- Report Number
- 1824206-2013-00754
- Event Type
- Malfunction
- Date Received
- January 29, 2013
- Date of Event
- January 20, 2013
- Report Date
- January 20, 2013
- 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 BED HAD A NEW UPPER CONTROL BOARD ON WHICH THE NURSE CALL FEATURE DID NOT ARRIVE AS ACTIVATED. TECHNICAL SUPPORT ASSISTED THE ACCOUNT IN ENABLING THE NURSE CALL FEATURE TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
THE TECHNICIAN ALLEGED THE NURSE CALL WAS DISABLED AND HAD TO BE MANUALLY ENABLED. NO PT IMPACT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 39777 | VERSACARE BED | A/C POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM, INC. | 3200 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |