Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Methylprednisolone acetate Injectable Suspension Recalled by Eugia US LLC 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 Eugia US LLC directly.
Affected Products
Methylprednisolone acetate Injectable Suspension, USP, 400mg per 5mL (80mg/mL, 5mL Multiple-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, NDC 55150-314-01
Quantity: 10,080 vials
Why Was This Recalled?
Failed Dissolution Specifications
Where Was This Sold?
This product was distributed to 4 states: LA, MS, OH, TN
About Eugia US LLC
Eugia US LLC has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report