Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Dutasteride Capsules Recalled by AVKARE Inc. Due to Failed Impurities/Degradation Specifications: High out of specification results...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact AVKARE Inc. directly.
Affected Products
Dutasteride Capsules, 0.5 mg, 30 Capsules (6 X 5) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-282-13.
Quantity: 3,989 cartons
Why Was This Recalled?
Failed Impurities/Degradation Specifications: High out of specification results for related compounds.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About AVKARE Inc.
AVKARE Inc. has 33 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report