FDA Adverse Event Malfunction Summary report: N

SECURE 3 MED/SURG BED

MDR report key: 2223154 · Received August 16, 2011

Report

Report Number
1831750-2011-08689
Event Type
Malfunction
Date Received
August 16, 2011
Date of Event
July 19, 2011
Report Date
July 19, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE CPU BOARD WAS BAD.

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