Nephron recalls phenylephrine injections due to lack of sterility assurance. Products may cause infections if used improperly. Check NDC 69374-301-10 and lot numbers PE2029.
Lack of Assurance of Sterility
Nephron is recalling phenylephrine injections that may not be sterile, posing infection risks. This affects medical users who need the medication for specific treatments.
The injections lack proper sterility assurance, meaning they could contain harmful bacteria. If used, this might lead to infections, especially in sensitive medical procedures.
Healthcare professionals and patients prescribed this injection for medical use. Those with compromised immune systems face higher infection risks.
Check for NDC 69374-301-10 on the packaging. Lot number PE2029 with expiration 06/17/2023. Products are sold in 30 vial packs per carton.
Look for NDC 69374-301-10 and lot number PE2029 on the packaging.
The recall states there is a lack of sterility assurance, so it may not be safe. Do not use until the remedy is confirmed.
Check for NDC 69374-301-10 and lot number PE2029 on the packaging. Products are sold in 30 vial packs per carton.
The recall does not specify a remedy, so contact Nephron directly for guidance.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0361-2023 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0361-2023 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.
