Nephron recalls phenylephrine injections with possible contamination. Products may cause infection if used. Check lot numbers on packaging for affected batches.
Lack of Assurance of Sterility
Nephron is recalling phenylephrine HCl injection vials that may not be sterile. Using these could lead to infections if the medication is contaminated. This is a serious safety issue for patients needing this drug.
The injections may not be sterile, meaning they could contain harmful bacteria or other contaminants. If injected, this could cause serious infections or other health issues.
Patients prescribed phenylephrine injections by a healthcare provider. Those using the recalled vials for medical treatment are at risk of infection.
Check the product label for lot numbers PE2025 through PE2035. The expiration dates range from May 28, 2023 to September 11, 2023. The product is sold by prescription only.
Immediately discard any recalled vials if you have them.
The product may not be sterile, which could lead to infections if used.
Lots PE2025 through PE2035 with expiration dates from May 28, 2023 to September 11, 2023.
Check the product label for lot numbers PE2025 through PE2035 with expiration dates from May 28, 2023 to September 11, 2023.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0359-2023 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0359-2023 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.
