# FDA recall Z-0174-2023

> **Becton Dickinson Infusion Therapy Systems Inc.** · Class II · device recall initiated 2022-10-12.

## 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)

## 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).

## Distribution

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

## Key facts

- **Recall number:** Z-0174-2023
- **Recalling firm:** Becton Dickinson Infusion Therapy Systems Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-10-12
- **Report date:** 2022-11-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sandy, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0174-2023

## Citation

> AI Analytics. FDA recall Z-0174-2023. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-0174-2023. Source: US FDA. Licensed CC0.

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