Nephron Sterile Compounding Center recalls norepinephrine injection with potential lack of sterility. Affected lots expire through March 2024. Consumers should contact manufacturer for details.
Lack of Assurance of Sterility
Nephron Sterile Compounding Center is recalling a specific norepinephrine injection product due to a lack of assurance of sterility. This could lead to infections if the medication is used without proper sterility.
The injection product lacks assurance of sterility, meaning it may contain harmful bacteria or other contaminants. If used in medical treatments, this could cause serious infections or other health complications.
Healthcare professionals and patients who have been prescribed this specific norepinephrine injection. Those using the product for medical treatments are at risk of infection.
Check the product label for the Nephron brand, 4 mg/250 mL norepinephrine bitartrate in 0.9% sodium chloride injection. Look for lot numbers NB2017A through NB2071A with expiration dates through March 2024.
Reach out to Nephron Sterile Compounding Center at 4500 12th St. Extension, West Columbia, SC 29172 for specific product details and instructions.
The recall states there is a lack of assurance of sterility, so the product may not be safe for medical use. Do not use without contacting the manufacturer.
Contact Nephron Sterile Compounding Center directly for instructions on what to do with the product.
Check the product label for lot numbers NB2017A through NB2071A with expiration dates through March 2024.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0357-2023 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0357-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
