FDA Adverse Event
Malfunction
Summary report: N
CENTRA BED
MDR report key: 2061953
·
Received March 18, 2011
Report
- Report Number
- 1824206-2011-01700
- Event Type
- Malfunction
- Date Received
- March 18, 2011
- Date of Event
- February 23, 2011
- Report Date
- February 23, 2011
- Manufacturer
- HILL-ROM INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- HI, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN ADJUSTED THE SIDERAIL LATCH TO REPAIR THE BED.
Description of Event or Problem · 1
INFORMATION RECEIVED INDICATES THE SIDERAIL WILL LATCH, BUT IF SHAKEN, THE SIDERAIL WOULD UNLATCH.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CENTRA BED | AC-POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM INC. | 850 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |