Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Flanax (aluminum hydroxide Recalled by Belmora LLC Due to Defective Container: Product lacks tamper evident breakaway band...
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 Belmora LLC directly.
Affected Products
Flanax (aluminum hydroxide, magnesium hydroxide, and simethicone) Fast Acting Antacid, 200 mg/200 mg/20 mg, 12 fl oz (355 mL) bottles, Distributed by: Belmora LLC, PO Box 3063, Arlington, VA 22203, UPC 8 53030 00209 0, NDC 27854.101.01.
Quantity: 17,996 bottles
Why Was This Recalled?
Defective Container: Product lacks tamper evident breakaway band on cap.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Belmora LLC
Belmora LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report