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Becton Dickinson & Company recalls CareFusion MaxPlus Clear Needleless Connector. Intended for Positive Displacement Connector for needleless access to the
Recalled October 16, 2019 · FDA recall Z-0049-2020 · Becton Dickinson &
Hazard
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. · FDA Class II
Units
115,200
Sold at
Nationwide Foreign: Canada
Description
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.
Product
CareFusion MaxPlus Clear Needleless Connector. Intended for Positive Displacement Connector for needleless access to the IV line and/or IV catheter during IV therapy Cat. No. MP1000-C
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →