Nephron recalls specific norepinephrine injections due to lack of sterility assurance. Affected lots expire by 2023-07-27. Contact for details.
Lack of Assurance of Sterility
Nephron Sterile Compounding Center is recalling norepinephrine injections that may not be sterile. This could lead to infections if used improperly. Patients should not use these products.
The injections lack assurance of sterility, meaning they could contain harmful bacteria or other contaminants. If used, this could cause serious infections or other health issues.
Healthcare professionals and patients who have the specific norepinephrine injection lots listed in the recall. Those using the product for medical treatment are most at risk.
Check the product label for the Nephron brand and the specific lot numbers: NB2018A through NB2068A. The expiration dates range from February 2023 to September 2023.
Immediately discard the recalled norepinephrine injection products if you have them.
Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection, USP, 16 mg/250 mL (64 mcg/mL*), 250 mL Single-Dose.
Lots: NB2018A, NB2022A, NB2028A, NB2032A, NB2036A, NB2043A, NB2046A, NB2049A, NB2052A, NB2062A, NB2068A.
Check the product label for the Nephron brand and the specific lot numbers listed 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-0358-2023 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0358-2023 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.