Non-Sterile BD Luer-Lok Tip Syringe Only recalled over sterility concerns
- Recall date
- January 27, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Becton Dickinson & Company recalls 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
- Recall number
- Z-1496-2026
- FDA classification
- Class II
- Brand / firm
- Becton Dickinson & Company
- Sold / distributed
- US Nationwide distribution in the states of California and Texas.
Why it was recalled
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
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