FDA Adverse Event
Malfunction
Summary report: N
HLL-ROM 100 LOW BED
MDR report key: 1794987
·
Received August 9, 2010
Report
- Report Number
- 1824206-2010-09214
- Event Type
- Malfunction
- Date Received
- August 9, 2010
- Date of Event
- July 12, 2010
- Report Date
- July 12, 2010
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- LA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN REPLACED THE MAIN CONTROLLER TO REPAIR THE BED.
Description of Event or Problem · 1
INFORMATION RECEIVED INDICATES THE BED HAS NO FUNCTIONS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HLL-ROM 100 LOW BED | AC POWERED HOSPITAL BED | FNL | HILL-ROM, INC. | 3930 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |