Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD BACTEC Plus Aerobic/F Culture Vials Recalled by Becton Dickinson & Co. Due to Certain vials of the BD BACTEC" Plus Aerobic/F...
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 & Co. directly.
Affected Products
BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023
Quantity: 781,600 vials
Why Was This Recalled?
Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling issue where duplicate barcode sequence numbers have been identified on more than one vial.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Becton Dickinson & Co.
Becton Dickinson & Co. has 183 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report