FDA Adverse Event
Injury
Summary report: N
ATLAS STRETCHER
MDR report key: 732752
·
Received July 7, 2006
Report
- Report Number
- 1831750-2006-00047
- Event Type
- Injury
- Date Received
- July 7, 2006
- Date of Event
- June 5, 2006
- Report Date
- June 7, 2006
- Manufacturer
- STRYKER CORP., MED DIV
- Product Code
- FPO
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WI, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT WHILE A PATIENT ORDERLY WAS TRANSPORTING A PATIENT UP A RAMP, THE STRETVHER ALLEGEDLY SLIPPED OUT OF GEAR AND THE ZOOM DRIVE STOPPED FUNCTIONING. REPORTEDLY, THE STRETCHER WITH 4 IV POLES STARTED TO SLIDE DOWN THE RAMP. THE ORDERLY HAS REPORTD PAIN IN HER BACK, HIPS AND LEG(S). SHE ALLEGEDLY WAS GIVEN PRESCIPTION PAIN MEDICATION AND IS BEING SEEN BY A CHIROPRACTOR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ATLAS STRETCHER | WHEELED HOSPITAL STRETCHER | FPO | STRYKER CORP., MED DIV | 0660 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Required Intervention |