Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Famotidine USP 20 mg Recalled by PD-Rx Pharmaceuticals, Inc. 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 PD-Rx Pharmaceuticals, Inc. directly.
Affected Products
Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30
Quantity: 100 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 PD-Rx Pharmaceuticals, Inc.
PD-Rx Pharmaceuticals, Inc. has 25 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report