FDA Adverse Event Malfunction Summary report: N

BD

MDR report key: 2072933 · Received April 1, 2011

Report

Report Number
1213809-2011-00001
Event Type
Malfunction
Date Received
April 1, 2011
Date of Event
February 8, 2011
Report Date
April 1, 2011
Manufacturer
BECTON DICKINSON DIVISION
Product Code
FMF
PMA / PMN Number
PRE-AMD
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

CRACKED SYRINGE BARREL RESULTING IN LOSS OF MEDICATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BD 10ML LUER LOK DISPOSABLE SYRINGE FMF BECTON DICKINSON DIVISION 10L10J

Patients

Seq Age Sex Outcome Treatment
1