Recall notification - MaxPlus Clear Needleless Connector

May 2, 2019

BD is conducting a voluntary medical device recall of one lot of the MaxPlus Clear Needleless Connector (catalog and lot number referenced in the table above). The recall is being conducted due to a lot specific defect, where after disconnection of a luer, the valve of the connector remains recessed; not fully closing, either temporarily or permanently. The risks of blood loss and air embolism exist if the valve remains permanently open and goes undetected, especially in the neonate population.

If you require further assistance, please contact Regional Customer Quality at 888-237-2762 Opt 3, Opt 2 Monday - Friday between 8AM and 5PM (CT).


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