FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE BARIATRIC
MDR report key: 1163379
·
Received September 10, 2008
Report
- Report Number
- 1824206-2008-03374
- Event Type
- Malfunction
- Date Received
- September 10, 2008
- Date of Event
- September 8, 2008
- Report Date
- September 8, 2008
- Manufacturer
- HILL-ROM RITTER
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- LA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
REPORTER STATED THAT THE RIGHT INTERMEDIATE SIDERAIL WILL NOT STAY UP. NO INJURY, SHE CALLED BACK TO SAY, THE ENG DEPT SPAYED THE SIDERAIL LATCH WITH WD-40 AND THIS CORRECTED THE PROBLEM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE BARIATRIC | AC POWERED HOSPITAL BED | FNL | HILL-ROM RITTER | 1840 | P1840ACA000009 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |