FDA Adverse Event
Summary report: N
POWER PRO AMBULANCE COT
MDR report key: 1121424
·
Received August 11, 2008
Report
- Report Number
- 1831750-2008-00110
- Date Received
- August 11, 2008
- Date of Event
- July 18, 2008
- Report Date
- July 18, 2008
- Manufacturer
- STRYKER CORP. - MEDICAL DIV.
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE REPORTED INCIDENT WAS LIKELY CAUSED BY NOT REMOVING THE COT FROM THE AMBULANCE IN ACCORDANCE WITH USER MANUAL. THE SAFETY HOOK WAS ALLEGEDLY MISSED WHEN THE COT WAS REMOVED ON AN ANGLE FROM THE AMBULANCE.
Description of Event or Problem · 1
IT WAS REPORTED THAT A COT DROPPED. NO PT OR USER INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | POWER PRO AMBULANCE COT | AMBULANCE COT | FPO | STRYKER CORP. - MEDICAL DIV. | 6500000000 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |