FDA Adverse Event Malfunction Summary report: N

SECURE II MED/SURG BED

MDR report key: 2841560 · Received October 22, 2012

Report

Report Number
1831750-2012-11071
Event Type
Malfunction
Date Received
October 22, 2012
Date of Event
September 24, 2012
Report Date
September 24, 2012
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

BRAKE CRANK ASSEMBLY.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BRAKES WERE NOT UNLOCKING. NO PATIENT 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 MEDICAL 3002 EX NA

Patients

Seq Age Sex Outcome Treatment
1