FDA Adverse Event Malfunction Summary report: N

GOBED II

MDR report key: 2092325 · Received May 3, 2011

Report

Report Number
1831750-2011-04274
Event Type
Malfunction
Date Received
May 3, 2011
Date of Event
April 6, 2011
Report Date
April 6, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

FAILED ACTUATOR NUT IN LIFT MOTOR.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE SCALE WILL NOT STAY ZEROED ON THE BED AND THE BED DRIFTS DOWN WHEN RAISED. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GOBED II A/C HOSPITAL BED FNL STRYKER MEDICAL FL28EX NA

Patients

Seq Age Sex Outcome Treatment
1 UNK