Darmerica Quinacrine Dihydrochloride (98.25%), bulk API product recall — FDA D-0125-2020
Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after testing, identified as Artemisinin.
Overview of recall records associated with Darmerica, LLC, including dates, categories and classifications where available.
Classification mix: Class I: 1.
Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after testing, identified as Artemisinin.
This page summarizes recall records in which the official source identifies Darmerica, LLC 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.