Nephron recalls phenylephrine injections due to lack of sterility assurance. Products may cause infections if used improperly. Check NDC 69374-956-10 for affected lots.
Lack of Assurance of Sterility
Nephron is recalling phenylephrine injections that may not be sterile, posing a risk of infection. This affects patients receiving the medication under medical supervision.
The injections lack proper sterility assurance, meaning they could contain harmful bacteria. If used, this might lead to infections, especially in vulnerable individuals.
Patients prescribed phenylephrine injections by healthcare providers. Those using the product without medical supervision are not affected.
Check for NDC code 69374-956-10 on the packaging. Products were sold in 5-syringe cartons labeled 'Nephron 503B outsourcing facility' with expiration date 10/3/2022.
Look for NDC 69374-956-10 on the packaging or check the expiration date (10/3/2022).
No, the product lacks sterility assurance and may cause infections. Do not use without contacting your healthcare provider.
Check for NDC code 69374-956-10 on the packaging or look for the expiration date 10/3/2022.
Contact your healthcare provider for guidance on safe handling or disposal.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1275-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1275-2022 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.
