Eugia recalls 200mg testosterone vials due to crystals not redissolving after warming. This affects patients using the injection for medical treatment. Contact Eugia for details.
cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
Eugia is recalling testosterone injections that may have crystals not dissolving after warming. This could affect medical treatment if the injection isn't properly prepared.
The vials may contain crystals that don't redissolve when warmed and shaken. This could lead to improper injection preparation if the crystals aren't dissolved before use.
Patients using the recalled testosterone injections for medical treatment. Those who have the specific vial with NDC 55150-277-01 and lot number 1TC24075A are most at risk.
Check for the vial labeled 'Testosterone Cypionate Injection, USP, CIII, 200mg per mL, Rx only, 1mL Single-Dose Vial' with NDC 55150-277-01 and lot number 1TC24075A.
Look for the NDC code 55150-277-01 and lot number 1TC24075A on the vial.
The recall is due to potential crystals not redissolving after warming, which could affect injection preparation. Patients should check the label and contact Eugia for guidance.
The recall does not specify a remedy, so contact Eugia US LLC directly for instructions.
Check the vial label for NDC 55150-277-01 and lot number 1TC24075A.
We’ve drafted a message you can send Eugia to request your refund or repair — edit it as you like.
Subject: Recall D-0363-2025 — Eugia Eugia Hello, I own a Eugia that is covered by recall D-0363-2025 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.