FDA Adverse Event Death Summary report: N

SECURE 3 MED/SURG BED

MDR report key: 1644342 · Received March 26, 2010

Report

Report Number
1831750-2010-00616
Event Type
Death
Date Received
March 26, 2010
Date of Event
March 16, 2010
Report Date
March 16, 2010
Manufacturer
STRYKER CORP., MEDICAL DIV.
Product Code
FNL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE FACILITY REPORTED TO THE SALES REPRESENTATIVE THE PT'S DAUGHTER WAS FOUND TO BE CONTINUALLY TURNING OFF THE BED EXIT SYSTEM.

Description of Event or Problem · 1

IT WAS REPORTED THAT AN ELDERLY FEMALE PT BECAME STUCK BETWEEN THE MATTRESS, AND THE SIDE RAILS AND PASSED AWAY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SECURE 3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 3002S3 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK Death