FDA Adverse Event Malfunction Summary report: N

POWER PRO AMBULANCE COT

MDR report key: 2883840 · Received November 15, 2012

Report

Report Number
1831750-2012-11958
Event Type
Malfunction
Date Received
November 15, 2012
Date of Event
October 19, 2012
Report Date
October 19, 2012
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

WHEEL.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE WHEEL WAS WORN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1