FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE
MDR report key: 2031734
·
Received March 21, 2011
Report
- Report Number
- 1824206-2011-01728
- Event Type
- Malfunction
- Date Received
- March 21, 2011
- Date of Event
- February 24, 2011
- Report Date
- February 24, 2011
- Manufacturer
- HILL-ROM INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NH, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN FOUND THE BED WAS IN REVERSE TRENDELENBURG BY 9 DEGREES AND WHEN HE OPERATED THE BED, HE FOUND THE FOOT HI/LOW DRIFTED WHEN OPERATING FROM HIGH TO LOW. THIS WAS CAUSED BY THE FOOT HI/LOW DOWN VALVE STICKING OPEN. HE REPLACED FOOT HI/LOW DOWN VALVE S-14 TO REPAIR THE BED.
Description of Event or Problem · 1
THE ACCOUNT ALLEGED A BED IN THE MAINTENANCE SHOP HAS THE FOOT HI/LOW DRIFTING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE | AC-POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM INC. | 1900 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |