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All product recalls associated with Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical.
Total Recalls
1000
Past Year
567
Class I (Serious)
25
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
CGMP Deviations: Presence of NDMA impurity detected in product.