Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Fenofibrate Capsules (Micronized) 200 mg Recalled by Impax Laboratories, Inc. Due to Labeling: Incorrect or Missing Lot and/or Exp. Date
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 Impax Laboratories, Inc. directly.
Affected Products
Fenofibrate Capsules (Micronized) 200 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0533-02
Quantity: 42,239 HDPE bottles ( 21,119,500 capsules)
Why Was This Recalled?
Labeling: Incorrect or Missing Lot and/or Exp. Date
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Impax Laboratories, Inc.
Impax Laboratories, Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report