FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE
MDR report key: 1232132
·
Received November 4, 2008
Report
- Report Number
- 1824206-2008-04023
- Event Type
- Malfunction
- Date Received
- November 4, 2008
- Date of Event
- October 7, 2008
- Report Date
- October 7, 2008
- Manufacturer
- HILL-ROM RITTER
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECH REPLACED THE HEAD HI/LOW SOLENOID VALVE TO REPAIR THE BED.
Description of Event or Problem · 1
INFO RECEIVED INDICATES THE BED DRIFTS INTO THE TRENDELENBURG POSITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE | AC POWERED HOSP BED | FNL | HILL-ROM RITTER | 1800 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |