FDA Adverse Event Malfunction Summary report: N

SECURE II MED/SURG BED

MDR report key: 1984634 · Received January 19, 2011

Report

Report Number
1831750-2011-00696
Event Type
Malfunction
Date Received
January 19, 2011
Date of Event
December 21, 2010
Report Date
December 21, 2010
Manufacturer
STRYKER CORP., MEDICAL DIV.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE SCALE DISPLAY IS NOT WORKING ON 3002 BED. NO PT INVOLVEMENT OR 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 CORP., MEDICAL DIV. 3002 NA

Patients

Seq Age Sex Outcome Treatment
1