Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Famotidine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed Tablet/Capsule Specification; out of specification for tablet...
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 Teva Pharmaceuticals USA directly.
Affected Products
Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60
Quantity: 28,188 bottles
Why Was This Recalled?
Failed Tablet/Capsule Specification; out of specification for tablet weight
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teva Pharmaceuticals USA
Teva Pharmaceuticals USA has 196 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report