Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Furosemide Tablets USP Recalled by Roxane Laboratories, Inc. Due to Failed Tablet/Capsule Specifications: An unusually thick tablet was...
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 Roxane Laboratories, Inc. directly.
Affected Products
Furosemide Tablets USP, 20 mg, 1000 count bottles, Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216, NDC 0054-4297-31.
Quantity: 6493 bottles
Why Was This Recalled?
Failed Tablet/Capsule Specifications: An unusually thick tablet was reported through a complaint.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Roxane Laboratories, Inc.
Roxane Laboratories, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report