FDA Adverse Event Malfunction Summary report: N

POWER PRO AMBULANCE COT

MDR report key: 2182046 · Received June 22, 2011

Report

Report Number
1831750-2011-06338
Event Type
Malfunction
Date Received
June 22, 2011
Date of Event
June 10, 2011
Report Date
June 10, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

HYDRAULIC SUB-ASSEMBLY CYLINDER.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE HYDRAULIC SUB-ASSEMBLY CYLINDER IS LEAKING ON THE COT. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1