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

Recalled October 2, 2019 · FDA recall D-0125-2020 · Darmerica

Hazard

Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after testing, identified as Artemisinin. · FDA Class I

Units

1.8 kilograms

Sold at

U.S.A. Nationwide

Description

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

Product

Quinacrine Dihydrochloride (98.25%), bulk API product, packaged in a) 500 g NDC# 71052-530-05; b) 50 g NDC# 71052-530-55, c) 25g NDC# 71052-530-25, Darmerica LLC 198 Wilshire Blvd Casselberry, FL 32707

Manufacturer(s)

Darmerica, LLC

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