FDA Enforcement Class II Terminated

BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G x 1 1/2 (1.2mm x 40mm) Catalog #309580 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection

Recall: Z-2750-2017 · Reported July 26, 2017

Enforcement

Recall Number
Z-2750-2017
Event ID
77513
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Becton Dickinson & Company
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 26, 2017
Initiation Date
September 16, 2016
Classification Date
July 19, 2017
Termination Date
March 20, 2018
Address
1 Becton Dr, N/A, Franklin Lakes, NJ, 07417-1815, United States

Description

BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G x 1 1/2 (1.2mm x 40mm) Catalog #309580 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection

Reason

BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required.

Code Info

6090832 2021-03 6176715 2021-06

Distribution

Nationwide Distribution

Quantity

340,000 units