FDA Adverse Event
Malfunction
Summary report: N
VERSACARE BED
MDR report key: 2042858
·
Received March 30, 2011
Report
- Report Number
- 1824206-2011-01948
- Event Type
- Malfunction
- Date Received
- March 30, 2011
- Date of Event
- March 9, 2011
- Report Date
- March 9, 2011
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECH FOUND THE LATCH PIN SCREW WAS SO TIGHT THAT THE PIN COULDN'T MOVE OUT TO LOCK. THE TECH LOOSENED THE SCREW TO REPAIR THE BED.
Description of Event or Problem · 1
INFO RECEIVED INDICATES THE SIDERAIL WOULDN'T LOCK IN THE UP POSITION.
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 |