Becton Dickinson & Company recalls Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose flu…

Recall date

March 25, 2016

Source

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

Recall number

Z-1936-2016

FDA classification

Class II

Brand / firm

Becton Dickinson & Company

Sold / distributed

Nationwide Distribution to NY only

Why it was recalled

BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm x 25 mm) and Henry Schein 10 mL Single Use Syringe Luer-Lock are being recalled due to possible adulteration and non-conforming manufacturing practices.

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

What was recalled

Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection