FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE
MDR report key: 2241353
·
Received September 2, 2011
Report
- Report Number
- 1824206-2011-04623
- Event Type
- Malfunction
- Date Received
- September 2, 2011
- Date of Event
- August 16, 2011
- Report Date
- August 16, 2011
- Manufacturer
- HILL-ROM INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN ISOLATED THE ISSUE TO THE SIDERAIL LATCH STICKING. HE LUBRICATED THE LATCH ASSEMBLY TO REPAIR THE BED.
Description of Event or Problem · 1
INFO RECEIVED INDICATES THE LEFT HEAD SIDERAIL IS NOT LATCHING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE | AC-POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM INC. | 1900 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |