FDA Adverse Event Injury Summary report: N

BD 60 ML LUER-LOC SYRINGE

MDR report key: 7013449 · Received November 9, 2017

Report

Report Number
MW5073189
Event Type
Injury
Date Received
November 9, 2017
Date of Event
November 7, 2017
Report Date
November 7, 2017
Manufacturer
BD
Product Code
FMF
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

WHILE IN THE COMPOUNDING ROOM I WENT TO GRAB A BD 60 ML. SYRINGE WITH LUER-LOC TIP. WHEN I PICKED ONE OUT OF THE BIN. I NOTICED THE INSIDE OF THE SYRINGE ON THE PLUNGER HAB A GREEN/BLACK RESIDUE. THE SYRINGE WAS STILL IN THE PACKAGING SO I SET IT ASIDE AND REPORTED IT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
792196 BD 60 ML LUER-LOC SYRINGE BD 60 ML LUER-LOC SYRINGE FMF BD 7086804

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention