FDA Adverse Event Malfunction Summary report: N

ADVANTAGE SERIES 26 OBS

MDR report key: 2031533 · Received March 21, 2011

Report

Report Number
1831750-2011-02608
Event Type
Malfunction
Date Received
March 21, 2011
Date of Event
February 24, 2011
Report Date
February 24, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE LEFT SIDERAIL WILL NOT LATCH. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1