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Darmerica Recalls

1 recall on record · October 2, 2019 to October 2, 2019 · Drugs

October 2, 2019DrugsFDA

Darmerica, LLC recalls Quinacrine Dihydrochloride (98.25%), bulk API product, packaged in a) 500 g NDC# 71052-530-05; b) 50 g NDC# 71052-530-55

Hazard: Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after testing, identified as Artemisinin.

Darmerica Recalls | RecallWatchUSA