FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE BARIATRIC PLUS BED
MDR report key: 3173471
·
Received June 11, 2013
Report
- Report Number
- 1824206-2013-03025
- Event Type
- Malfunction
- Date Received
- June 11, 2013
- Date of Event
- May 15, 2013
- Report Date
- May 15, 2013
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN TRIED TO REPAIR THIS BED THE FAMILY OF THE PATIENT WOULD NOT ALLOW THE TECHNICIAN TO REPAIR THE BED. NO FURTHER INFO IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.
Description of Event or Problem · 1
THE ACCOUNT ALLEGED THAT THE RIGHT SIDE RAIL WOULD NOT RISE. NO PATIENT IMPACT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 264163 | TOTALCARE BARIATRIC PLUS BED | A/C POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM, INC. | 1840 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |