FDA Adverse Event
Malfunction
Summary report: N
POWER PRO AMBULANCE COT
MDR report key: 2142813
·
Received June 20, 2011
Report
- Report Number
- 1831750-2011-06185
- Event Type
- Malfunction
- Date Received
- June 20, 2011
- Date of Event
- May 23, 2011
- Report Date
- May 23, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- INK
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
RESTRAINT STRAPS.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE RESTRAINTS NEEDED TO BE REPLACED ON THE COT DUE TO WEAR. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | POWER PRO AMBULANCE COT | STRETCHER, WHEELED | INK | STRYKER MEDICAL | 6500 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |