GenoGenix recalls all EDTA injection products due to lack of sterility assurance. This could lead to infections if used improperly. Contact the manufacturer for details.
Lack of Assurance of Sterility
GenoGenix is recalling all EDTA injection products because they may not be sterile. Using these products could cause infections if they are not properly sterilized.
The product may not be sterile, which means it could cause infections if used in medical procedures. This is a serious concern for any medical injection.
People who have received EDTA injections from this manufacturer are affected. Healthcare providers and patients using these products are at risk.
Check for the product name 'EDTA for Injection' and the manufacturer 'GenoGenix LLC'. All lots within the expiry date are included in this recall.
Look for the product name 'EDTA for Injection' and the manufacturer 'GenoGenix LLC' on the label.
The recall states there is a lack of sterility assurance, so it may not be safe to use. Contact the manufacturer for more details.
The recall does not specify a remedy, so contact GenoGenix LLC for guidance on next steps.
Yes, the recall includes all strengths and presentations of EDTA injections from GenoGenix LLC.
We’ve drafted a message you can send GenoGenix to request your refund or repair — edit it as you like.
Subject: Recall D-0073-2026 — GenoGenix GenoGenix Hello, I own a GenoGenix that is covered by recall D-0073-2026 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.
