FDA Adverse Event Malfunction Summary report: N

ADVANTAGE SERIES 26

MDR report key: 2870579 · Received November 14, 2012

Report

Report Number
1831750-2012-11914
Event Type
Malfunction
Date Received
November 14, 2012
Date of Event
October 17, 2012
Report Date
October 17, 2012
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Removal / Correction Number
Z-227-08
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

BRAKE CAM.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BRAKES WOULD NOT REMAIN ENGAGED. THE CUSTOMER REPORTED THAT THEY DID NOT KNOWN IF THERE WAS PATIENT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ADVANTAGE SERIES 26 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1009 NA

Patients

Seq Age Sex Outcome Treatment
1