Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed Content Uniformity 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 Allergan Sales, LLC directly.
Affected Products
TAZORAC (tazarotene) Gel 0.05%, Rx only, For Dermatologic Use Only, Not for Ophthalmic Use, packaged in a) 30 g tubes (NDC: 0023-8335-03, UPC: 300238335036) and b)100 g tubes,(NDC: 0023-8335-10, UPC: 300238335104), Manufactured by: Allergan Inc., Irvine, CA 92512.
Quantity: 25,247 tubes (19,499 30 gram/ 5,748 100 gram)
Why Was This Recalled?
Failed Content Uniformity Specifications
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Allergan Sales, LLC
Allergan Sales, LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report