FDASeptember 16, 2016device

BD 10mL Syringe Luer-Lok Tip Catalog number 301997 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.

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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BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection — Recall Details · AllClear