FDA Adverse Event Malfunction Summary report: N

POWER PRO AMBULANCE COT

MDR report key: 2031801 · Received February 25, 2011

Report

Report Number
1831750-2011-01915
Event Type
Malfunction
Date Received
February 25, 2011
Date of Event
January 28, 2011
Report Date
January 30, 2011
Manufacturer
STRYKER MEDICAL
Product Code
INK
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE STRYKER MX PRO WOULD NOT LOCK INTO PLACE AND THE COT WENT FROM LOAD POSITION TO THE GROUND. THERE WAS REPORTED PATIENT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

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