FDA Adverse Event Malfunction Summary report: N

CUB PEDIATRIC CRIB - HYD BASE

MDR report key: 2933497 · Received December 21, 2012

Report

Report Number
1831750-2012-13228
Event Type
Malfunction
Date Received
December 21, 2012
Date of Event
November 27, 2012
Report Date
November 27, 2012
Manufacturer
STRYKER MEDICAL
Product Code
FMS
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL WOULD DROP QUICKLY DUE TO A BROKEN SIDE RAIL ASSIST CABLE; SIDE RAIL COULD NOT BE LATCHED IN THE RAISED POSITION. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CUB PEDIATRIC CRIB - HYD BASE PEDIATRIC OPEN HOSPITAL BED FMS STRYKER MEDICAL FL19H NA

Patients

Seq Age Sex Outcome Treatment
1