Eugia US LLC recalls 400mg per 5mL Methylprednisolone acetate Injectable Suspension due to failed dissolution specifications. This medication is for prescription use only and was manufactured in India. Consumers should contact the manufacturer for details.
Failed Dissolution Specifications
Eugia US LLC is recalling a specific prescription medication because it failed dissolution tests. This means the medication may not work properly when injected, which could affect treatment effectiveness. The recall applies to certain lots manufactured in India.
The medication failed dissolution specifications, meaning it may not release the active ingredient properly when injected. This could lead to ineffective treatment if the medication does not work as intended. However, the recall does not specify a risk of injury or harm to the patient.
Prescription patients using the recalled Methylprednisolone acetate Injectable Suspension. Those with the specific lot numbers (3MA23001-3MA23003) and expiration date 3/31/2025 are most at risk.
Check the product label for the lot numbers 3MA23001, 3MA23002, or 3MA23003. The expiration date is 3/31/2025. This medication is a prescription-only injectable suspension.
Look for lot numbers 3MA23001, 3MA23002, or 3MA23003 on the vial.
The recall states the medication failed dissolution specifications, but does not indicate it is unsafe. Patients should contact Eugia US LLC for further details.
Check the product label for the lot numbers 3MA23001-3MA23003. If you have these lots, contact Eugia US LLC for instructions.
The recall does not specify any risk of injury or harm to the patient. The hazard is related to treatment effectiveness, not physical injury.
We’ve drafted a message you can send Eugia to request your refund or repair — edit it as you like.
Subject: Recall D-0366-2024 — Eugia Eugia Hello, I own a Eugia that is covered by recall D-0366-2024 from Eugia. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
