FDAJuly 6, 2021device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Due to high glucose test results when using the blood collection cards.

What to do

FDA enforcement status: Terminated

Brands named

advance dxadvance

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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 — Recall Details · AllClear