Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BBL DrySlide Oxidase Kit Recalled by Becton Dickinson & Co. Due to In-vitro diagnostic agents were placed into incorrect packaging...
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
BBL DrySlide Oxidase Kit, catalog number 231746 Product Usage: Presumptive diagnostic aid for gram-negative bacteria.
Quantity: 610 total test kits (PYR and Oxidase)
Why Was This Recalled?
In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories.
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