Advance Dx 100 Blood Collection Card Quantity 25 REF CMT01 Advance Dx 100 Blood Collection recall — FDA Z-2237-2021
Due to high glucose test results when using the blood collection cards.
Overview of recall records associated with Advance Dx, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Due to high glucose test results when using the blood collection cards.
This page summarizes recall records in which the official source identifies Advance Dx, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.