Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bexarotene Capsules Recalled by Upsher Smith Laboratories, Inc. Due to Failed Dissolution Specifications
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 Upsher Smith Laboratories, Inc. directly.
Affected Products
Bexarotene Capsules, 75 mg, 100 capsules per bottle, Rx Only, Manufactured for: Upsher-Smith Laboratories, LLC, Maple Grove, MN 55369. NDC: 0832-0285-00
Quantity: 166 bottles
Why Was This Recalled?
Failed Dissolution Specifications
Where Was This Sold?
This product was distributed to 4 states: KY, LA, NJ, OH
About Upsher Smith Laboratories, Inc.
Upsher Smith Laboratories, Inc. has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report