FDA Adverse Event
Malfunction
Summary report: N
FLUOROSCOPY STRETCHER
MDR report key: 1853035
·
Received September 21, 2010
Report
- Report Number
- 1831750-2010-02485
- Event Type
- Malfunction
- Date Received
- September 21, 2010
- Date of Event
- August 18, 2010
- Report Date
- August 26, 2010
- Manufacturer
- STRYKER CORP, MEDICAL DIV.
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT BOTH JACKS RAISE BUT DECLINE 4 INCHES AFTER 15 MINUTES USE. IT IS FURTHER REPORTED THAT THE HYDRAULIC FLUID WAS FOUND AT THE BASE OF THE JACKS. THERE WAS NO PT INVOLVEMENT. NO ADVERSE CONSEQUENCES WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | FLUOROSCOPY STRETCHER | HOSPITAL WHEELED STRETCHER | FPO | STRYKER CORP, MEDICAL DIV. | 1080 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |