Nephron recalls phenylephrine injections due to lack of sterility assurance. Affected lots expire through 2022. Consumers should contact Nephron for details.
Lack of Assurance of Sterility
Nephron is recalling phenylephrine injections that may not be sterile. This could cause infections if used improperly. The product is only available by prescription.
The injections lack proper sterility assurance, meaning they could contain harmful bacteria. Using non-sterile injections can lead to infections, especially in medical settings.
Prescription patients who received this specific phenylephrine injection from Nephron. Those with medical conditions requiring injections are most at risk.
Check for Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172. Look for lots PE2001A through PE2014A with expiration dates through October 2022.
Identify the lot number and expiration date on the syringe packaging.
Reach out to Nephron Sterile Compounding Center LLC for specific recall instructions.
The recall indicates a lack of sterility assurance, so it is not safe to use. Contact Nephron for details.
Check for Nephron 503B facility, lots PE2001A through PE2014A, and expiration dates through October 2022.
Contact Nephron Sterile Compounding Center LLC for specific instructions on handling the product.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1274-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1274-2022 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.
