Becton Dickinson Infusion Therapy Systems Inc.: Medical Device Recall in 2022 - (Recall #: Z-0174-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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)

Product Classification:

Class II

Date Initiated: October 12, 2022

Date Posted: November 9, 2022

Recall Number: Z-0174-2023

Event ID: 90972

Reason for Recall:

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).

Status: Ongoing

Product Quantity: 56,080 units

Code Information:

Catalog Number: 383516 UDI-DI Code: (01)00382903835164 Lot Number: 2168865

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated