FDA Adverse Event Malfunction Summary report: N

SECURE II MED/SURG BED

MDR report key: 2231205 · Received July 18, 2011

Report

Report Number
1831750-2011-07163
Event Type
Malfunction
Date Received
July 18, 2011
Date of Event
June 19, 2011
Report Date
June 19, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RESULT: FAULTY BRAKE CRANK ASSEMBLY.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BED HAD A BRAKE FORCE DEFICIENCY. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1