FDA Adverse Event
Malfunction
Summary report: N
RENAISSANCE 26 STRETCHER
MDR report key: 1882835
·
Received October 21, 2010
Report
- Report Number
- 1831750-2010-03120
- Event Type
- Malfunction
- Date Received
- October 21, 2010
- Date of Event
- September 23, 2010
- Report Date
- September 23, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIVISION
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END JACK WILL NOT RISE UP. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | RENAISSANCE 26 STRETCHER | HOSPITAL WHEELED STRETCHER | FPO | STRYKER CORP., MEDICAL DIVISION | 1211 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |