FDASeptember 16, 2016device

BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required of 10-6.

What to do

FDA enforcement status: Terminated

Brands named

becton dickinsonbectonbecton dickinson

UPCs

606174620210260829822021026089821202103611785820210461178632021046117889202104611789120210461469622021046173697202105617376720210661737792021066208614202107

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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