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Becton Dickinson Infusion Therapy Systems Inc. recalls BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1 x 25 mm) 61 mL/min (3660 mL/hr)
Recalled November 9, 2022 · FDA recall Z-0174-2023 · Becton Dickinson Infusion Therapy Systems
Hazard
During needle withdrawal, the tip shield may prematurely separate from the catheter adapter and preventing the needle tip from being in the safely shielded (leaving the needle tip exposed). · FDA Class II
Units
56,080 units
Sold at
U.S.: New York, Florida, Maryland, North Carolina, Virginia, Georgia, Rhode Island, New Jersey, Pennsylvania, Illinois, South Carolina, Maine, and Massachusetts. O.U.S.: N/A
Description
During needle withdrawal, the tip shield may prematurely separate from the catheter adapter and preventing the needle tip from being in the safely shielded (leaving the needle tip exposed).
Product
BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1 x 25 mm) 61 mL/min (3660 mL/hr)
Manufacturer(s)
Becton Dickinson Infusion Therapy Systems Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →