FDA Adverse Event
Malfunction
Summary report: N
ESACARE BED
MDR report key: 2942230
·
Received January 4, 2013
Report
- Report Number
- 1824206-2013-00103
- Event Type
- Malfunction
- Date Received
- January 4, 2013
- Date of Event
- December 19, 2012
- Report Date
- December 19, 2012
- Manufacturer
- HILL-ROM INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NC, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN CALIBRATED THE POWER CONTROL BOARD TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
THE TECHNICIAN ALLEGED THE BED WOULD NOT PLACE A NURSE CALL. NO PT IMPACT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 5704 | ESACARE BED | AC POWERED ADJUSTALBE HOSPITAL BED | FNL | HILL-ROM INC. | 3200 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |