Nephron recalls sterile amino acid injection bags (NDC 69374-988-10) due to lack of sterility assurance. Patients may face infection risks from contaminated products.
Lack of Assurance of Sterility
Nephron Sterile Compounding Center is recalling amino acid injection bags that may not be sterile. This could lead to infections if used improperly.
The bags lack proper sterility assurance, meaning they could be contaminated with bacteria or other pathogens. If used without proper sterilization, this could cause infections in patients.
Healthcare providers and patients who received these specific amino acid injection bags for medical use. Those with compromised immune systems are at higher risk.
Check for the NDC code 69374-988-10 on the bag. The product was manufactured by Nephron Sterile Compounding Center LLC in West Columbia, SC, with lots AA2012A and expiration 07/04/2022.
Look for the NDC code 69374-988-10 on the bag label.
The recall states there is a lack of sterility assurance, so these bags may not be safe for medical use. Do not use without confirming the recall.
The recall record does not specify a replacement process or remedy.
The recalled product expires on 07/04/2022.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1245-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1245-2022 from Nephron. 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.
