FDA Adverse Event
Malfunction
Summary report: N
VERSACARE BED
MDR report key: 2841715
·
Received October 22, 2012
Report
- Report Number
- 1824206-2012-06700
- Event Type
- Malfunction
- Date Received
- October 22, 2012
- Date of Event
- October 3, 2012
- Report Date
- October 3, 2012
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NJ, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN FOUND THE CASTERS WERE WORN. HE REPLACED THE CASTERS TO REPAIR THE BED.
Description of Event or Problem · 1
INFORMATION RECEIVED INDICATES THE CASTES CONTINUE TO RATCHET WHEN IN BRAKE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VERSACARE BED | AC-POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM, INC. | 3200 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |