FDA Adverse Event Malfunction Summary report: N

ST104 TRANSPORT

MDR report key: 1823280 · Received August 27, 2010

Report

Report Number
1831750-2010-01923
Event Type
Malfunction
Date Received
August 27, 2010
Date of Event
July 27, 2010
Report Date
August 2, 2010
Manufacturer
STRYKER CORP, MEDICAL DIVISION
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

THE CUSTOMER REPORTED VIA THE FIELD SERVICE ENGINEER THAT THE JACK HAS FAILED. IT IS FURTHER REPORTED THAT THE JACK LEAKED A LARGE AMOUNT OF CLEAR OIL ONTO THE FLOOR. THERE WERE NO ADVERSE CONSEQUENCES REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ST104 TRANSPORT HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MEDICAL DIVISION 0737 NA

Patients

Seq Age Sex Outcome Treatment
1 NA