FDA Adverse Event
Malfunction
Summary report: N
SM104 MSERIES W5TH WHL
MDR report key: 1813231
·
Received August 18, 2010
Report
- Report Number
- 1831750-2010-01868
- Event Type
- Malfunction
- Date Received
- August 18, 2010
- Date of Event
- July 27, 2010
- Report Date
- July 27, 2010
- Manufacturer
- STRYKER CORP, MEDICAL DIV
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NL
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT THE SIDERAIL IS NOT LATCHING UP.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SM104 MSERIES W5TH WHL | HOSPITAL WHEELED STRETCHER | FPO | STRYKER CORP, MEDICAL DIV | 1005 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |