FDA Adverse Event Malfunction Summary report: N

SECURE II MED/SURG BED

MDR report key: 2033379 · Received March 22, 2011

Report

Report Number
1831750-2011-02644
Event Type
Malfunction
Date Received
March 22, 2011
Date of Event
February 23, 2011
Report Date
February 23, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WV, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RESULT: LOAD CELL.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BED SCALE DID NOT WORK. THERE WAS PT INVOLVEMENT, HOWEVER, NO 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 BED FNL STRYKER MEDICAL 3002 EX NA

Patients

Seq Age Sex Outcome Treatment
1