FDA Adverse Event
Malfunction
Summary report: N
STRETCHER
MDR report key: 1893768
·
Received November 2, 2010
Report
- Report Number
- 1831750-2010-03487
- Event Type
- Malfunction
- Date Received
- November 2, 2010
- Date of Event
- October 13, 2010
- Report Date
- October 13, 2010
- Manufacturer
- STRYKER CORP, MEDICAL DIVISION
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE BRAKES ARE NOT WORKING. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | STRETCHER | HOSPITAL WHEELED STRETCHER | FPO | STRYKER CORP, MEDICAL DIVISION | 1010 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |