FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE
MDR report key: 1132424
·
Received August 22, 2008
Report
- Report Number
- 1824206-2008-03177
- Event Type
- Malfunction
- Date Received
- August 22, 2008
- Date of Event
- August 12, 2008
- Report Date
- August 12, 2008
- Manufacturer
- HILL-ROM RITTER
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
REP ALLEGED THE HI/LOW UP HAD UNINTENTIONAL MOVEMENT. NO INJURY REPORTED. UNIT MOVING ERRATICALLY CAUSE - U.C.M. DAMAGED BY FLUID BUILD UP, RESOLVE - REPLACED U.C.M.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE | AC POWERED HOSPITAL BED | FNL | HILL-ROM RITTER | 1900 | P1900F005565 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |