GenoGenix recalls all Ultra Burn for Injection products due to lack of sterility assurance. This could lead to infections if used improperly. Consumers should contact the company for details.
Lack of Assurance of Sterility
GenoGenix is recalling all Ultra Burn for Injection products because they may not be sterile. This could cause infections if the product is used.
The product may not be sterile, which means it could cause infections if injected. This is a serious risk for medical use.
People who have purchased Ultra Burn for Injection products from any source are affected. Those using the product for medical purposes are at higher risk.
Check the product label for the brand name 'GenoGenix' and product name 'Ultra Burn for Injection'. All lots within the expiry date are included in this recall.
Reach out to GenoGenix LLC at 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692 for recall details.
The recall states there is a lack of sterility assurance, which could lead to infections. 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.
The recall includes all lots within the expiry date, but specific lot numbers are not mentioned in the record.
We’ve drafted a message you can send GenoGenix to request your refund or repair — edit it as you like.
Subject: Recall D-0068-2026 — GenoGenix GenoGenix Hello, I own a GenoGenix that is covered by recall D-0068-2026 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.
