FDA Adverse Event
Malfunction
Summary report: N
TOTALCARE
MDR report key: 1121969
·
Received August 13, 2008
Report
- Report Number
- 1824206-2008-03074
- Event Type
- Malfunction
- Date Received
- August 13, 2008
- Date of Event
- April 25, 2008
- Report Date
- April 25, 2008
- Manufacturer
- HILL-ROM RITTER
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IN 2008- CUSTOMER STATED THAT HEAD SECTION WAS DAMAGED. I FOUND THAT THE HEAD SECTION WELDMENT WAS BENT AND TORN FROM PIVOT SLIDE SLOTS ALSO DAMAGING WEIGH FRAME WELDMENT. IN 2008 - CUSTOMER STATED THAT HE IS NOT SURE WHAT CAUSED THE HEAD SECTION TO BECOME DAMAGED. NO INJURIES REPORTED AT THIS TIME. BED WAS TRADED IN FOR NEW BED, AND BROUGHT BACK TO HILL-ROM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTALCARE | AC POWERED HOSPITAL BED | FNL | HILL-ROM RITTER | 1900 | PR1900B000010 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |