FDA Adverse Event Malfunction Summary report: N

GO BED PLUS

MDR report key: 2021498 · Received February 16, 2011

Report

Report Number
1831750-2011-01491
Event Type
Malfunction
Date Received
February 16, 2011
Date of Event
January 21, 2011
Report Date
January 21, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL LOCKOUT LIGHTS ARE NOT WORKING ON THE FOOTBOARD. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GO BED PLUS A/C HOSPITAL BED FNL STRYKER MEDICAL 2501 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK