FDA Adverse Event
Malfunction
Summary report: N
CENTRA BED
MDR report key: 1874469
·
Received October 12, 2010
Report
- Report Number
- 1824206-2010-10435
- Event Type
- Malfunction
- Date Received
- October 12, 2010
- Date of Event
- September 18, 2010
- Report Date
- September 18, 2010
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IN, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN FOUND THE CPR ENGAGEMENT ON THE HEAD DRIVE SCREW WOULD NOT RE-ENGAGE AND THE CPR WAS ENGAGED SLIGHTLY ENOUGH THAT THE HEAD WOULD NOT STAY UP. THE TECHNICIAN REPLACED THE HEAD DRIVE ASSEMBLY TO REPAIR THE BED.
Description of Event or Problem · 1
INFORMATION RECEIVED INDICATES THE HEAD OF THE BED SLOWLY LOWERED ON ITS OWN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CENTRA BED | AC POWERED HOSPITAL BED | FNL | HILL-ROM, INC. | 850 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |