Nephron recalls Oxytocin 30 Units/500 mL IV bags due to lack of sterility assurance. Affected lots expire 7/9/2022. Contact for return instructions.
Lack of Assurance of Sterility
Nephron is recalling Oxytocin IV bags that may not be sterile. This could lead to infections if used in medical treatments. Patients should not use these bags without contacting their healthcare provider.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. If used in medical procedures, this could cause infections or other health issues.
Healthcare providers and patients who have received this specific Oxytocin IV bag from the recalled lots. Those using the product for medical treatments are most at risk.
Check for the NDC code 69374-543-50 on the packaging. The product was sold in lots OX2013C and OX2013E, expiring 7/9/2022. It was packaged in 10 x 1 IV bags per case.
Look for the NDC code 69374-543-50 and lots OX2013C or OX2013E on the packaging.
The product lacks assurance of sterility, so it should not be used without contacting your healthcare provider.
Check for NDC code 69374-543-50 and lots OX2013C or OX2013E on the packaging.
Contact your healthcare provider for guidance on safe disposal or alternative options.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1273-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1273-2022 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.
