FDA Adverse Event Injury Summary report: N

BD BECTON DICKINSON ECLIPSE NEEDLE

MDR report key: 2792445 · Received October 10, 2012

Report

Report Number
MW5027232
Event Type
Injury
Date Received
October 10, 2012
Date of Event
October 9, 2012
Report Date
October 10, 2012
Manufacturer
BECTON DICKINSON
Product Code
FMI
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
NM, US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

I AM A PHARMACIST WHO HAS BEEN GIVING FLU SHOTS USING BECTON DICKINSON ECLIPSE INJECTION NEEDLES PRODUCT (B)(4), NDC #(B)(4). TWICE IN THE LAST YEAR I HAVE HAD THE PROTECTIVE NEEDLE COVER BREAK OFF AFTER GIVING AN INJECTION. THE COVER IS SUPPOSED TO SWING UP AND COVER THE TOP BUT TWICE I HAVE HAD THIS COVER BREAK OFF LEAVING MY FINGER MOVING TOWARD AN EXPOSED NEEDLE. THIS IS SUPPOSED TO BE PROTECTING HEALTHCARE PROVIDERS FROM NEEDLE STICKS BUT IT ACTUALLY MAKES YOU MORE PRONE AS YOU SWING YOUR FINGER TOWARD AN EXPOSED NEEDLE THAT HAS JUST BEEN USED FOR AN INJECTION. I SENT BD THE BROKEN DEVICE LAST YEAR WHEN THIS OCCURRED AND THEY BASICALLY SAID THAT THEY HAD NO OTHER PROBLEMS WITH THIS DEVICE AS IF IT WERE AN ISOLATED INCIDENT. SINCE IT HAS HAPPENED TO ME TWICE I DOUBT THAT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BD BECTON DICKINSON ECLIPSE NEEDLE ECLIPSE INJECTION NEEDLE .5MM X 25 MM FMI BECTON DICKINSON 0169750

Patients

Seq Age Sex Outcome Treatment
1 49 YR Life Threatening