FDA Adverse Event
Malfunction
Summary report: N
VERSACARE
MDR report key: 1190645
·
Received October 3, 2008
Report
- Report Number
- 1824206-2008-03692
- Event Type
- Malfunction
- Date Received
- October 3, 2008
- Date of Event
- September 29, 2008
- Report Date
- September 29, 2008
- Manufacturer
- HILL-ROM RITTER
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- DC, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
TECH REPLACED THE SIDECOM BOARD, AND NURSE CALL FUNCTIONED PROPERLY.
Description of Event or Problem · 1
HILL-ROM TECHNICIAN REPORTED THAT THE NURSE MANAGER TOLD HIM THAT THIS BED WOULD NOT PLACE A NURSE CALL. HE REPORTED THAT THERE WERE NO INJURIES REPORTED. HE SAID THAT THE PT WAS USING A PENDANT TO CALL THE NURSE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VERSACARE | AC POWERED HOSPTIAL BED | FNL | HILL-ROM RITTER | P3200 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |