FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE
MDR report key: 1823311
·
Received August 30, 2010
Report
- Report Number
- 1824206-2010-09640
- Event Type
- Malfunction
- Date Received
- August 30, 2010
- Date of Event
- August 5, 2010
- Report Date
- August 5, 2010
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE ACCOUNT FOUND THE F5 FUSE WAS OUT. THE TECHNICIAN REPLACED THE FUSE TO REPAIR THE BED.
Description of Event or Problem · 1
THE ACCOUNT ALLEGED THE BED HAS NO FUNCTIONS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE | AC POWERED HOSPITAL BED | FNL | HILL-ROM, INC. | 1900 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |