FDA Adverse Event
Malfunction
Summary report: N
POWER PRO AMBULANCE COT
MDR report key: 1833963
·
Received September 9, 2010
Report
- Report Number
- 1831750-2010-02155
- Event Type
- Malfunction
- Date Received
- September 9, 2010
- Date of Event
- August 16, 2010
- Report Date
- August 16, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIV.
- Product Code
- INK
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
HYDRAULIC LEAK.
Description of Event or Problem · 1
IT HAS BEEN REPORTED BY THE CUSTOMER THAT THE COT IS LEAKING HYDRAULIC FLUID. THE COT WAS STILL FULLY FUNCTIONING IN MANUAL AND POWER MODE. NO ADVERSE CONSEQUENCES OR INJURIES HAVE BEEN REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | POWER PRO AMBULANCE COT | STRETCHER WHEELED | INK | STRYKER CORP., MEDICAL DIV. | 6500 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |