Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
D-10 Dual Program Recalled by Bio-Rad Laboratories, Inc. Due to D-10 A1c Dual Program Floppy was programmed incorrectly...
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 Bio-Rad Laboratories, Inc. directly.
Affected Products
D-10 Dual Program, which contains Update Kit D-10 A1c program diskette. United States; Bio-Rad Laboratories, Hercules, CA 94547 The Bio-Rad D-10 Hemoglobin Testing System provides an integrated method for the separation and determination of the relative percent of specific hemoglobins (e.g., A2, F, Ale} in whole blood. The separation is based on the principles of high performance liquid chromatography.
Quantity: 2906 kits (318 Kits in US; 2588 kits internationally)
Why Was This Recalled?
D-10 A1c Dual Program Floppy was programmed incorrectly and cartridge injections counts are not being updated correctly when switching between the D-10 Dual Short Program and Extended Program on the D-10 Hemoglobin Testing System.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bio-Rad Laboratories, Inc.
Bio-Rad Laboratories, Inc. has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report