GenoGenix recalls all Epithalon 20mg injections due to lack of sterility assurance. This could lead to infections if used. Consumers should contact the manufacturer for details.
Lack of Assurance of Sterility
GenoGenix is recalling all Epithalon 20mg injections because they may not be sterile. Using these products could cause infections if they are contaminated.
The product may not be sterile, which means it could contain harmful bacteria. If injected, this could lead to infections or other health issues.
People who have purchased Epithalon 20mg injections from GenoGenix. Those with medical conditions requiring injections are most at risk.
Check for the product name 'Epithalon for Injection, 20mg' and the lot number GG053025-002. The product was manufactured by GenoGenix LLC.
Reach out to GenoGenix LLC at 2840 NW 2nd Ave Ste 204, Boca Raton, FL 33431-6692 for specific instructions.
The recall states there is a lack of sterility assurance, so it may not be safe. Do not use the product until contacted by GenoGenix.
Contact GenoGenix LLC at 2840 NW 2nd Ave Ste 204, Boca Raton, FL 33431-6692 for instructions on what to do with the product.
Yes, the lot number GG053025-002 is associated with this recall.
We’ve drafted a message you can send GenoGenix to request your refund or repair — edit it as you like.
Subject: Recall D-0089-2026 — GenoGenix GenoGenix Hello, I own a GenoGenix that is covered by recall D-0089-2026 from GenoGenix. 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.
