FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE
MDR report key: 1163300
·
Received September 9, 2008
Report
- Report Number
- 1824206-2008-03343
- Event Type
- Malfunction
- Date Received
- September 9, 2008
- Date of Event
- September 3, 2008
- Report Date
- September 3, 2008
- Manufacturer
- HILL-ROM RITTER
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AZ, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
NO INJURY BEING REPORTED, REP STATED THAT THIS BED HAD NO FUNCTION. REP REPLACED THE F5 FUSE TO REPAIR THIS BED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE | AC POWERED HOSPITAL BED | FNL | HILL-ROM RITTER | 1900 | PR1900HK000027 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |