Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Voriconazole Tablets Recalled by AVKARE Inc. Due to Failed impurities/degradation specifications: Out of specification for a...
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
Voriconazole Tablets, 200 mg, 20-count cartons (4 x 5) Unit Dose, Rx only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 50268-804-12
Quantity: 1172 cartons (23440 tablets)
Why Was This Recalled?
Failed impurities/degradation specifications: Out of specification for a related compound C.
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