FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE BARIATRIC PLUS BED
MDR report key: 2942238
·
Received January 4, 2013
Report
- Report Number
- 1824206-2013-00109
- Event Type
- Malfunction
- Date Received
- January 4, 2013
- Date of Event
- May 24, 2011
- Report Date
- December 18, 2012
- Manufacturer
- HILL-ROM INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN REPLACED THE TRENDELENBERG VALVE TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
THE TECHNICIAN ALLEGED THAT THE BED HAD NO TRENDELENBURG FUNCTION. NO PT IMPACT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 4884 | TOTALCARE BARIATRIC PLUS BED | AC POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM INC. | 1840 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |