# FDA recall Z-0125-2021

> **Becton Dickinson & Company** · Class II · device recall initiated 2020-09-14.

## Product

BD Nexiva Closed IV Catheter System   Dual Port (20 GA 1.75 IN)  Catalog (Ref) No. 383538    BD Nexiva closed IV catheter systems are intended to be inserted into a patient s vascular system for short term use to sample blood, monitor blood pressure, or administer fluids.

## Reason for recall

Dull/blunt needles within the IV Catheter System may lead to missed insertion attempts and delay in diagnosis or treatment until a new needle is  inserted

## Distribution

US: Nationwide Distribution: AK, AR, AZ, CA, IL, KS, MO, NY, OH, UT, VA; and International to: Canada and Mexico.

## Key facts

- **Recall number:** Z-0125-2021
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-09-14
- **Report date:** 2020-10-28
- **Termination date:** 2021-09-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Franklin Lakes, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0125-2021

## Citation

> AI Analytics. FDA recall Z-0125-2021. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-0125-2021. Source: US FDA. Licensed CC0.

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