FDA Adverse Event
Malfunction
Summary report: N
RESIDENT BED
MDR report key: 2823562
·
Received October 8, 2012
Report
- Report Number
- 1824206-2012-06217
- Event Type
- Malfunction
- Date Received
- October 8, 2012
- Date of Event
- September 14, 2012
- Report Date
- September 14, 2012
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
NO FURTHER INFO IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.
Description of Event or Problem · 1
THE ACCOUNT ALLEGEDLY THEY HAD UNPLUGGED THE BED AND WHEN PLUGGING IT BACK IN THE HI/LOW, HEAD AND KNEE SECTIONS ALL RAN UP TO THEIR UPPER LIMITS. NO PT IMPACT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | RESIDENT BED | A/C POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM, INC. | 870 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |