FDA Adverse Event
Malfunction
Summary report: N
MX-PRO R-3 AMBULANCE COT
MDR report key: 2142754
·
Received June 20, 2011
Report
- Report Number
- 1831750-2011-06168
- Event Type
- Malfunction
- Date Received
- June 20, 2011
- Date of Event
- August 5, 2010
- Report Date
- August 5, 2010
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
HEIGHT ADJUSTMENT RACK.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE COT WOULD NOT RAISE OR LOWER PROPERLY AND THE RACK ASSEMBLY WAS BENT. IT IS UNK IF THERE WAS PT INVOLVEMENT OR ADVERSE CONSEQUENCES REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MX-PRO R-3 AMBULANCE COT | STRETCHER, WHEELED | FPO | STRYKER MEDICAL | 6082 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |