Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Advance Dx 100 Blood Collection Card Quantity 25 REF CMT01 Recalled by Advance Dx, Inc. Due to Due to high glucose test results when using...
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 Advance Dx, Inc. directly.
Affected Products
Advance Dx 100 Blood Collection Card Quantity 25 REF CMT01 Advance Dx 100 Blood Collection Card and Foil Bags Quantity 500 Cards and Foil Bags REF CMT01/F02 IFU: Advance Dx 100 SSE(Serum Separating Extraction) Technology BLOOD COLLECTION INSTRUCTIONS
Quantity: 179,750 cards
Why Was This Recalled?
Due to high glucose test results when using the blood collection cards.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Advance Dx, Inc.
Advance Dx, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report