Nephron recalls phenylephrine injections with potential sterility issues. Affected lots expire by 2023; check your NDC number for recall.
Lack of Assurance of Sterility
Nephron is recalling phenylephrine injections that may not be sterile. This could lead to infections if used improperly. Consumers should stop using these products immediately.
The injections lack assurance of sterility, meaning they could contain harmful bacteria or other contaminants. Using these products might cause infections, especially in medical settings where sterility is critical.
Patients prescribed phenylephrine injections by healthcare providers. Those with the specific lot numbers and expiration dates listed are most at risk.
Check the NDC number on the packaging: 69374-957-10. Look for lot numbers PE2004A through PE2019C with expiration dates up to April 2023.
Discard the product if you have the recalled lot numbers and expiration dates listed in the recall notice.
No, the product lacks assurance of sterility and could cause infections. Do not use.
Lot numbers PE2004A through PE2019C with specific expiration dates listed in the recall notice.
Check the NDC number on the packaging (69374-957-10) and verify the lot number and expiration date against the list provided in the recall.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1276-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1276-2022 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.
