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

Recalled July 26, 2017 · FDA recall Z-2753-2017 · Becton Dickinson &

Hazard

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

Units

1,528,000 units

Sold at

Nationwide Distribution

Description

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

Product

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

Manufacturer(s)

Becton Dickinson & Company

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →