Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due to Nonsterile syringe potentially exposing the patient to pathogenic...
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
BD Ultra-Fine Insulin Syringe 1mL, 12.7mm, 29G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326719
Quantity: 80,500 units
Why Was This Recalled?
Nonsterile syringe potentially exposing the patient to pathogenic microorganisms and a risk of local infection.
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