FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE BED
MDR report key: 3033173
·
Received March 1, 2013
Report
- Report Number
- 1824206-2013-01190
- Event Type
- Malfunction
- Date Received
- March 1, 2013
- Date of Event
- February 4, 2013
- Report Date
- February 4, 2013
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN FOUND THE POSITION OF THE MATTRESS WAS CAUSING THE SIDERAIL TO NOT LATCH. THE MATTRESS WAS REPOSITIONED TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
THE TECHNICIAN ALLEGED THE SIDERAIL WOULD NOT LATCH. NO INJURY REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 90289 | TOTALCARE BED | A/C POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM, INC. | 1900 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |