FDA Adverse Event
Malfunction
Summary report: N
EYE SURGERY STRETCHER
MDR report key: 1972317
·
Received December 30, 2010
Report
- Report Number
- 1831750-2010-05413
- Event Type
- Malfunction
- Date Received
- December 30, 2010
- Date of Event
- December 2, 2010
- Report Date
- December 2, 2010
- Manufacturer
- STRYKER CORP., MED DIV
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MI, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE BRAKE CONTROLS ARE NOT WORKING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | EYE SURGERY STRETCHER | HOSPITAL WHEELED STRETCHER | FPO | STRYKER CORP., MED DIV | 1079 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |