Nephron recalls phenylephrine injections due to lack of sterility assurance. Products may cause infections if used improperly. Check NDC numbers and expiration dates for affected lots.
Lack of Assurance of Sterility
Nephron is recalling phenylephrine injections that may not be sterile, posing infection risks. This recall affects specific lots with expiration dates up to August 2022. Users should check their product details to confirm if they have recalled items.
The injections lack proper sterility assurance, meaning they could become contaminated and cause infections if used. This risk is particularly concerning for medical procedures where sterile conditions are critical.
People who have received phenylephrine injections from Nephron's specific lots (PE1108A, PE2006A, PE2010A) with expiration dates up to August 2022. Healthcare providers and patients using these injections are most at risk.
Check the NDC number 69374-955-10 on the product label. Look for expiration dates: PE1108A (exp. 5/27/2022), PE2006A (exp. 8/3/2022), or PE2010A (exp. 8/12/2022).
Verify the NDC number 69374-955-10 and expiration dates to confirm if your product is affected.
Phenylephrine HCl Injection, USP, 0.4 mg/10 mL (40 mcg/mL), 10 mL Pre-Filled Syringes, 5 x 10 mL Pre-Filled Syringes, 6 x 5 Syringe Carton.
Check the NDC number 69374-955-10 and expiration dates: PE1108A (exp. 5/27/2022), PE2006A (exp. 8/3/2022), or PE2010A (exp. 8/12/2022).
The recall does not specify a remedy, so 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-0965-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0965-2022 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.
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.
