Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Desoximetasone Gel USP Recalled by Akorn, Inc. Due to Failed impurities/degradation specifications: product was out of specification...
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 Akorn, Inc. directly.
Affected Products
Desoximetasone Gel USP, 0.05%, packaged in 60 gram aluminum tubes, Rx only, Marketed by: VersaPharm Incorporated Marietta, GA 30062, Manufactured by: Ei LLC Kannapolis, NC 28083, NDC 61748-205-60.
Quantity: 4,045 units
Why Was This Recalled?
Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Akorn, Inc.
Akorn, Inc. has 176 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report