FDA Adverse Event Malfunction Summary report: N

SECURE II MED/SURG BED

MDR report key: 2000117 · Received February 18, 2011

Report

Report Number
1831750-2011-01547
Event Type
Malfunction
Date Received
February 18, 2011
Date of Event
January 24, 2011
Report Date
January 24, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RESULTS: TIMING LINK, SIDERAIL PANEL.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD LEFT SIDERAIL COULD NOT BE LOCKED IN THE TOP POSITION. IT WAS FURTHER REPORTED, THERE WERE DAMAGED SIDERAIL PANELS. IT IS UNK IF THERE WAS PT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SECURE II MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002 NA

Patients

Seq Age Sex Outcome Treatment
1