GenoGenix recalls all Biotin for Injection products due to lack of sterility assurance. This could pose infection risks if used improperly.
Lack of Assurance of Sterility
GenoGenix is recalling all Biotin for Injection products because they may not be sterile. This could lead to infections if the product is used.
The product lacks sterility assurance, meaning it might not be safe for injection. This could cause infections if used improperly.
People who have purchased Biotin for Injection from GenoGenix. Those using the product for medical purposes are most at risk.
Check for GenoGenix Biotin for Injection products with any lot number. All strengths and presentations are affected.
Look for the product name and lot number on the packaging.
The recall states there is a lack of sterility assurance, so it may not be safe for injection.
The recall record does not mention any remedy or replacement options.
The recall record does not specify any action steps for affected products.
We’ve drafted a message you can send GenoGenix to request your refund or repair — edit it as you like.
Subject: Recall D-0048-2026 — GenoGenix GenoGenix Hello, I own a GenoGenix that is covered by recall D-0048-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
