FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE BARIATRIC PLUS BED
MDR report key: 2941626
·
Received January 2, 2013
Report
- Report Number
- 1824206-2013-00024
- Event Type
- Malfunction
- Date Received
- January 2, 2013
- Date of Event
- December 17, 2012
- Report Date
- December 17, 2012
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN COULD NOT FIND AN ISSUE WITH THE BED, THE BED FUNCTIONED AS DESIGNED.
Description of Event or Problem · 1
THE ACCOUNT ALLEGED THAT THE HEAD SECTION WILL NOT RAISE. NO PT IMPACT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1450 | TOTALCARE BARIATRIC PLUS BED | AC POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM, INC. | 1840 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |