Nephron recalls phenylephrine injection vials due to lack of sterility assurance. This could lead to infections if used improperly. Check your product details to see if you have affected items.
Lack of Assurance of Sterility
Nephron is recalling phenylephrine injection vials that may not be sterile, which could cause infections if used. This is a serious safety issue for medical users who need the medication.
The injection vials lack assurance of sterility, meaning they might contain harmful bacteria. If used without proper sterilization, this could lead to infections or other health issues.
Medical professionals and patients prescribed this injection are affected. Those using the product without proper sterility checks are at highest risk.
Check for the product name: Phenylephrine HCl Injection, USP, 0.4 mg/10 mL (40 mcg/mL), 10 mL Single-Dose Vial. Look for lot numbers PE2028 with expiration date 06/15/2023.
Immediately stop using the recalled phenylephrine injection vials as they may not be sterile.
No, the product lacks sterility assurance and should not be used.
Check for lot number PE2028 with expiration date 06/15/2023 on the vial packaging.
Stop using it immediately and contact Nephron Sterile Compounding Center LLC for further instructions.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0360-2023 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0360-2023 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.
