FDA Adverse Event Malfunction Summary report: N

SECURE II MED/SURG BED

MDR report key: 2841529 · Received October 22, 2012

Report

Report Number
1831750-2012-11028
Event Type
Malfunction
Date Received
October 22, 2012
Date of Event
September 26, 2012
Report Date
September 26, 2012
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

RESULT: FOWLER MOTOR.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER WOULD NOT STAY IN THE UP POSITION WITH WEIGHT. NO PATIENT 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 BED FNL STRYKER MEDICAL 3002 NA

Patients

Seq Age Sex Outcome Treatment
1