FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE
MDR report key: 1112733
·
Received August 11, 2008
Report
- Report Number
- 1824206-2008-03032
- Event Type
- Malfunction
- Date Received
- August 11, 2008
- Date of Event
- July 9, 2008
- Report Date
- July 9, 2008
- Manufacturer
- HILL-ROM RITTER
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OR, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IN 2008, REP STATED THE BED HAS NO FUNCTIONS. HE SAID NOBODY WAS HURT. TWO DAYS LATER, REP CALLED IN STATING BED IS BACK IN SERVICE. HE REPLACED THE F1 FUSE AND THIS TOOK CARE OF PROBLEM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE | AC POWERED HOSPITAL BED | FNL | HILL-ROM RITTER | 1900 | P1900D004731 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |