FDA Adverse Event Malfunction Summary report: N

CUB PEDIATRIC CRIB - HYD BASE

MDR report key: 2113561 · Received May 24, 2011

Report

Report Number
1831750-2011-05008
Event Type
Malfunction
Date Received
May 24, 2011
Date of Event
April 26, 2011
Report Date
April 26, 2011
Manufacturer
FLEXTRONICS EMS CANADA
Product Code
FMS
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UT, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

BRAKE RING ON WHEELS AND BRAKE PEDAL NOT COMPLETELY UNLOCKING BRAKES.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BRAKE AND STEER FUNCTIONS WERE NOT WORKING PROPERLY. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CUB PEDIATRIC CRIB - HYD BASE BED, PEDIATRIC OPEN HOSPITAL FMS FLEXTRONICS EMS CANADA FL19H NA

Patients

Seq Age Sex Outcome Treatment
1 UNK