FDA Adverse Event
Injury
Summary report: N
TOTALCARE BED
MDR report key: 2782058
·
Received September 28, 2012
Report
- Report Number
- 1824206-2012-05954
- Event Type
- Injury
- Date Received
- September 28, 2012
- Date of Event
- September 11, 2012
- Report Date
- September 12, 2012
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE HILL-ROM TECHNICIAN FOUND THAT THE HYDRAULIC MANIFOLD WAS CONTAMINATED. HE FOUND THAT SOMETIMES THE HEAD UP FUNCTION WORKED AND OTHER TIMES IT DID NOT WORK. HE REPLACED THE HYDRAULIC MANIFOLD AND THE BED FUNCTIONED TO DESIGN SPECIFICATIONS.
Description of Event or Problem · 1
INFO RECEIVED INDICATED THE HEAD SECTION WAS OPERATING INTERMITTENTLY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE BED | AC-POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM, INC. | 1900 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |