FDA Adverse Event Malfunction Summary report: N

GO BED PLUS

MDR report key: 2110450 · Received April 25, 2011

Report

Report Number
1831750-2011-03953
Event Type
Malfunction
Date Received
April 25, 2011
Date of Event
March 29, 2011
Report Date
March 29, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

BENT AND BROKEN SIDE CONTROL PEDAL.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BED HAS A BROKEN SIDE CONTROL PEDAL. IT IS UNK IF THERE WAS PT INVOLVEMENT OR 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