Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. Recalled by Becton Dickinson & Company Due to During the bulk packaging process, some Luer Slip...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Becton Dickinson & Company directly.
Affected Products
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
Quantity: 204,000 units
Why Was This Recalled?
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Becton Dickinson & Company
Becton Dickinson & Company has 169 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report