FDA Adverse Event Malfunction Summary report: N

SECURE 3 MED/SURG BED

MDR report key: 2110316 · Received May 20, 2011

Report

Report Number
1831750-2011-04919
Event Type
Malfunction
Date Received
May 20, 2011
Date of Event
April 27, 2011
Report Date
April 27, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

RESULT: ADHESIVE CAUSING THE BUTTON TO STICK.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD OF THE BED GOES DOWN AFTER RAISING IT. IT WAS REPORTED THAT THE CUSTOMER DOES NOT KNOW IF THERE WAS ANY PT INVOLVEMENT OR IF THERE WERE ANY ADVERSE CONSEQUENCES RELATED TO THE ALLEGED ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SECURE 3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002S3EX NA

Patients

Seq Age Sex Outcome Treatment
1