# FDA recall Z-1496-2026

> **Becton Dickinson & Company** · Class II · device recall initiated 2026-01-27.

## Product

10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.

## Reason for recall

During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.

## Distribution

US Nationwide distribution in the states of California and Texas.

## Key facts

- **Recall number:** Z-1496-2026
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-27
- **Report date:** 2026-03-18

- **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-1496-2026

## Citation

> AI Analytics. FDA recall Z-1496-2026. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1496-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*