Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Testosterone Cypionate + Progesterone Recalled by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical Due to CGMP Deviations
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 Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical directly.
Affected Products
Testosterone Cypionate + Progesterone, 200 mg/ 2.5 mg/mL ,10 mL amber glass vials, Rx Only, Compounded by AXIA Pharmaceutical, Los Angeles, CA 90025
Quantity: 120 vials
Why Was This Recalled?
CGMP Deviations
Where Was This Sold?
There were only one customer in California
About Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical
Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical has 64 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report