FDA Adverse Event Malfunction Summary report: N

POWER PRO AMBULANCE COT

MDR report key: 2222472 · Received July 13, 2011

Report

Report Number
1831750-2011-07019
Event Type
Malfunction
Date Received
July 13, 2011
Date of Event
June 15, 2011
Report Date
June 15, 2011
Manufacturer
STRYKER MEDICAL
Product Code
INK
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE RETAINING POST WAS LOOSE. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE 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