FDA Adverse Event Summary report: N

CUB CRIB

MDR report key: 1911551 · Received November 22, 2010

Report

Report Number
9680128-2010-00322
Date Received
November 22, 2010
Date of Event
October 15, 2010
Report Date
October 15, 2010
Manufacturer
STRYKER MEDICAL QUEBEC, LP
Product Code
FMS
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT A CUB CRIB WITH BRAKES NOT WORKING. NO INJURY REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 UNK