Alerts and Notices


Medical device recall for BD PosiFlush™ Heparin Lock Flush Syringes and BD™ Pre-Filled Normal Saline Syringes

Out of an abundance of caution and in the interest of public health, BD is voluntarily recalling certain lots of BD PosiFlush™ Heparin Lock Flush and BD™ Pre-Filled Normal Saline Flush syringes due to a potential for contamination with Serratia marcescens bacterium. BD was notified by the U.S. Food and Drug Administration (FDA) and Centers for Disease Control and Prevention (CDC) about a potential epidemiological link between catheter related blood stream infections and the S. marcescens bacterium. To date, there is no evidence of BD flush product testing positive for this bacterium.

Resources

Customer letter
Full list of affected lot numbers

Search by Catalog/Lot Information

You may enter multiple Lot Numbers to determine if the lots are being recalled, or you may enter a Catalog No. to see all lots being recalled under that Catalog No. Please enter either a six digit catalog number or a seven alphanumeric lot number below.