FDA Adverse Event Malfunction Summary report: N

ADVANTAGE SERIES 26

MDR report key: 2090964 · Received May 11, 2011

Report

Report Number
1831750-2011-04534
Event Type
Malfunction
Date Received
May 11, 2011
Date of Event
April 13, 2011
Report Date
April 13, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL COULD NOT BE LATCHED UP. IT IS UNK IF THERE WAS PT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ADVANTAGE SERIES 26 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1001 NA

Patients

Seq Age Sex Outcome Treatment
1