# FDA recall Z-1710-2019

> **Becton Dickinson & Company** · Class II · device recall initiated 2019-03-01.

## Product

BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system   Catalog Number: 383536

## Reason for recall

Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.

## Distribution

US distribution to one distributor in VA.

## Key facts

- **Recall number:** Z-1710-2019
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-01
- **Report date:** 2019-06-12
- **Termination date:** 2020-05-21

- **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-1710-2019

## Citation

> AI Analytics. FDA recall Z-1710-2019. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1710-2019. Source: US FDA. Licensed CC0.

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