FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE
MDR report key: 1780154
·
Received May 7, 2010
Report
- Report Number
- 1824206-2010-06976
- Event Type
- Malfunction
- Date Received
- May 7, 2010
- Date of Event
- April 12, 2010
- Report Date
- April 12, 2010
- Manufacturer
- HILL-ROM INC.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Description of Event or Problem · 1
TECHNICIAN ALLEGED SIDERAIL WOULD NOT LATCH. HE FOUND E-RINGS MISSING ON LATCH PIN. HE REPLACED MISSING PART TO RESOLVE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE | AC POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM INC. | P1900K006231 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |