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
Reported: October 2, 2019 Initiated: September 6, 2019 #D-0125-2020
Product Description
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
Reason for Recall
Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after testing, identified as Artemisinin.
Details
- Recalling Firm
- Darmerica, LLC
- Units Affected
- 1.8 kilograms
- Distribution
- U.S.A. Nationwide
- Location
- Casselberry, FL
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Darmerica, LLC. Units affected: 1.8 kilograms.
Why was this product recalled? ▼
Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after testing, identified as Artemisinin.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 2, 2019. Severity: Critical. Recall number: D-0125-2020.
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