FDA Adverse Event
Summary report: N
POWERFLEXX AMBULANCE COT
MDR report key: 3834818
·
Received May 12, 2014
Report
- Report Number
- 1523574-2014-00008
- Date Received
- May 12, 2014
- Report Date
- May 9, 2014
- Manufacturer
- FERNO-WASHINGTON, INC.
- Product Code
- FPO
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Additional Manufacturer Narrative · 1
THE DEVICE HAS BEEN EVALUATED BY THE MANUFACTURER AND THE INCIDENT COULD NOT BE DUPLICATED AND NO MALFUNCTION WAS DETECTED. WE ARE REPORTING THIS INCIDENT DUE TO THE REPORTED DELAY IN TRANSPORT.
Description of Event or Problem · 1
CUSTOMER STATED THAT WHILE ON THE SCENE OF AN AUTO ACCIDENT, THEY ATTEMPTED TO LOAD A FULL ARREST PATIENT AND EXPERIENCED DIFFICULTY LOWERING THE COT TO A LOAD POSITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 283275 | POWERFLEXX AMBULANCE COT | POWERFLEXX AMBULANCE COT | FPO | FERNO-WASHINGTON, INC. | 0115654 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 11 YR |