Eugia US LLC has recalled 36,816 vials of Testosterone Cypionate Injection, USP (200mg per mL) because users reported that crystals in the liquid would not dissolve even after warming and shaking the vials. This recall affects 1mL single-dose vials manufactured by Eugia Specialties Limited and distributed across the United States. If you use this medication, check your vial to see if it is part of the affected lot.
Injecting a solution containing undissolved crystals can cause physical irritation, inflammation, or damage to blood vessels and tissue at the injection site or elsewhere in the body.
You have 2 options:
Recall #: D-0363-2025; Manufactured by Eugia Specialties Limited, Telangana State, India.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.