FDA Adverse Event Injury Summary report: N

POWER PRO AMBULANCE COT

MDR report key: 2921906 · Received January 10, 2013

Report

Report Number
1831750-2013-90129
Event Type
Injury
Date Received
January 10, 2013
Date of Event
December 7, 2012
Report Date
December 10, 2012
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

OPERATOR FAILED TO ENSURE THAT THE SAFETY HOOK IN THE AMBULANCE ENGAGED WITH THE SAFETY BAR OF THE COT.

Description of Event or Problem · 1

IT HAS BEEN REPORTED THAT AN OPERATOR ALLEGEDLY INCURRED AN INJURY FROM THE COT TIPPING OVER WHILE BEING UPLOADED FROM AN AMBULANCE. IT WAS REPORTED THAT THE INJURY INVOLVED A RIGHT ARM AND SHOULDER INJURY, WHICH WAS DESCRIBED AS A STRAIN/SPRAIN, AND WHICH REPORTEDLY REQUIRED AN ER VISIT. THERE WAS NO PT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
16011 POWER PRO AMBULANCE COT WHEELED, STRETCHER FPO STRYKER MEDICAL 6500 NA

Patients

Seq Age Sex Outcome Treatment
1 Other