FDA Adverse Event Malfunction Summary report: N

CUB PEDIATRIC CRIB-FIXED BASE

MDR report key: 2141408 · Received June 1, 2011

Report

Report Number
1831750-2011-05366
Event Type
Malfunction
Date Received
June 1, 2011
Date of Event
May 4, 2011
Report Date
May 4, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FMS
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

BROKEN SIDERAIL ASSIST CABLE.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE RIGHT SIDERAIL WAS DIFFICULT TO MOVE. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CUB PEDIATRIC CRIB-FIXED BASE BED, PEDIATRIC OPEN HOSPITAL FMS STRYKER MEDICAL FL19F NA

Patients

Seq Age Sex Outcome Treatment
1 UNK