Becton Dickinson & Company recalls BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use, Hypodermic Syringe is intended for use by health care p…

Recall date

September 16, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2753-2017

FDA classification

Class II

Brand / firm

Becton Dickinson & Company

Sold / distributed

Nationwide Distribution

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection