Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Kiestra" Isolate Suspension Cuvette Array Recalled by Becton Dickinson & Co. Due to The 2D barcodes on these cuvettes contain formatting...
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 Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
Quantity: 29,760 units
Why Was This Recalled?
The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state and the cuvettes cannot be used.
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