FDA Adverse Event Malfunction Summary report: N

SECURE II MED/SURG BED

MDR report key: 2000113 · Received February 18, 2011

Report

Report Number
1831750-2011-01551
Event Type
Malfunction
Date Received
February 18, 2011
Date of Event
January 20, 2011
Report Date
January 20, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RESULT: DAMAGED FOWLER BALL SCREW, FOWLER WELDMENT LINK AND FOWLER LINK BRACKET.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER WAS STUCK AT 35 DEGREES AND COULD NOT BE LOWERED TO A FLAT POSITION. 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