GenoGenix recalls all Pentosan 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 strengths and presentations of Pentosan for Injection because the product may not be sterile. This could lead to infections if the medication is used.
The product may not be sterile, which can lead to infections if injected. This is a serious concern for medical use as infections can cause severe complications.
Patients who have been prescribed Pentosan for Injection are affected. Those using the medication without proper sterility checks are at higher risk.
Check for the product name 'Pentosan for Injection' from GenoGenix LLC. All lots within expiry are included in this recall.
Identify if you have Pentosan for Injection from GenoGenix LLC.
The recall states there is a lack of sterility assurance, so it is not safe to use without the remedy.
The recall does not specify a remedy, so no action is required beyond checking if you have the product.
The recall does not provide specific instructions, so contact GenoGenix LLC for further guidance.
We’ve drafted a message you can send GenoGenix to request your refund or repair — edit it as you like.
Subject: Recall D-0078-2026 — GenoGenix GenoGenix Hello, I own a GenoGenix that is covered by recall D-0078-2026 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.
