Nephron recalls 1000mL Cardioplegia Solution IV bags with potential contamination. These are prescription-only products used in cardiac surgery. Contact Nephron for details on affected lots and remedies.
Lack of Assurance of Sterility
Nephron is recalling certain Cardioplegia Solution IV bags due to a lack of sterility assurance. This could lead to infections if used in cardiac surgery. Patients and healthcare providers should not use these products.
The solution may not be sterile, which could cause infections during cardiac surgery. This is a serious risk because the product is used in critical medical procedures.
Healthcare providers and patients who have prescription-only Cardioplegia Solution 1000mL IV bags from Nephron. Those using the recalled products for cardiac surgery are most at risk.
Check for the NDC code 69374-984-10 on the packaging. The affected lots are NC2031A through NC2035A with expiration dates between July 7, 2022 and July 19, 2022.
Immediately stop using the recalled Cardioplegia Solution IV bags if you have them.
The NDC code is 69374-984-10.
Lots NC2031A, NC2033A, NC2034A, and NC2035A.
Expiration dates range from July 7, 2022 to July 19, 2022.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1269-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1269-2022 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.
