FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE SPORT
MDR report key: 2943503
·
Received January 9, 2013
Report
- Report Number
- 1824206-2013-00219
- Event Type
- Malfunction
- Date Received
- January 9, 2013
- Date of Event
- December 26, 2012
- Report Date
- December 26, 2012
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE HILL-ROM TECHNICIAN FOUND THAT THERE WAS SOME DRIED FLUID BUILT UP ON THE SIDERAIL LATCH COMPONENTS KEEPING THE SIDERAIL FROM LATCHING. HE CLEANED THE SIDERAIL LATCHING COMPONENTS TO REPAIR THE BED.
Description of Event or Problem · 1
INFO RECEIVED INDICATED THE LEFT SIDERAIL WOULD NOT LATCH.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 12872 | TOTALCARE SPORT | AC POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM, INC. | 1900 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |