FDA Adverse Event Malfunction Summary report: N

CUB PEDIATRIC CRIB- HYD BASE

MDR report key: 2150213 · Received June 10, 2011

Report

Report Number
1831750-2011-05811
Event Type
Malfunction
Date Received
June 10, 2011
Date of Event
May 16, 2011
Report Date
May 16, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FMS
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

BROKEN OUTER SPRING IN HANDLE ASSEMBLY.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE RIGHT SIDE RAIL RELEASE HANDLE WAS BROKEN. 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 STRYKER MEDICAL FL19H NA

Patients

Seq Age Sex Outcome Treatment
1 UNK