Advance Dx, Inc. recalls Advance Dx 100 Blood Collection Card Quantity 25 REF CMT01 Advance Dx 100 Blood Collection Card and Foil Bags Quanti

Recalled August 18, 2021 · FDA recall Z-2237-2021 · Advance Dx

Hazard

Due to high glucose test results when using the blood collection cards. · FDA Class II

Units

179,750 cards

Sold at

U.S. Nationwide distribution in the states of MD and NC.

Description

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

Product

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

Manufacturer(s)

Advance Dx, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →