FDA Adverse Event
Other
Summary report: N
THE ROSE BED
MDR report key: 1918107
·
Received November 30, 2010
Report
- Report Number
- 9680128-2010-00354
- Event Type
- Other
- Date Received
- November 30, 2010
- Date of Event
- November 4, 2010
- Report Date
- November 16, 2010
- Manufacturer
- STRYKER MEDICAL QUEBEC LP
- Product Code
- FNL
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT DURING THE COURSE OF CARE, A PATIENT WAS TURNED ON HER SIDE. REPORTEDLY, THE SIDE RAIL GAVE WAY AND THE PT FELL ONTO THE FLOOR. THE REPORT STATED THAT THE RESIDENT WAS TRANSFERRED TO THE HOSPITAL AND WAS DIAGNOSED WITH A BROKEN FINGER, HEAD LACERATION, AND RIGHT HIP FRACTURE. IT WAS REPORTED THAT BEING ON PALLIATIVE CARE AND DNR/DNI STATUS, THE RESIDENT WAS NOT A SURGICAL CANDIDATE AND AS RETURNED TO THE (B)(6) CENTER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | THE ROSE BED | HOSPITAL BED, A-C POWERED, ADJUSTABLE | FNL | STRYKER MEDICAL QUEBEC LP | FL14E1 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK | Hospitalization| O |