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Becton Dickinson & Company recalls BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson Infus
Recalled April 1, 2015 · FDA recall Z-1317-2015 · Becton Dickinson &
Hazard
Becton Dickinson received an elevated number of complaints for blood or infusate/medication leakage due to tearing of the silicone septum. · FDA Class II
Units
315,800 units
Sold at
Distributed to the states of CA, CT, FL, IL, MA, ND, NY, OH and PA.
Description
Becton Dickinson received an elevated number of complaints for blood or infusate/medication leakage due to tearing of the silicone septum.
Product
BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson Infusion Therapy Systems Inc. An accessory to an intravascular administration set that permits injection, gravity flow or withdrawal of fluids.
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →