GenoGenix recalls all L-Arginine 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 L-Arginine for Injection products because they may not be sterile. Using these products could lead to infections if they are not properly sterilized.
The product lacks assurance of sterility, meaning it might contain harmful bacteria or other contaminants. This could cause infections if the product is used without proper sterilization.
Patients receiving L-Arginine injections for medical treatment. Those with compromised immune systems are at higher risk of infection.
Check for the product name 'L-Arginine for Injection' from GenoGenix LLC. All lots within the expiry date are affected.
Identify the product name and manufacturer to confirm if it is recalled.
The recall indicates a lack of sterility assurance, so it is not safe to use without proper sterilization.
Look for the product name 'L-Arginine for Injection' from GenoGenix LLC. All lots within the expiry date are affected.
The recall does not specify a remedy, so contact GenoGenix for further instructions.
We’ve drafted a message you can send GenoGenix to request your refund or repair — edit it as you like.
Subject: Recall D-0055-2026 — GenoGenix GenoGenix Hello, I own a GenoGenix that is covered by recall D-0055-2026 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.
