Nephron recalls phenylephrine HCl injection due to lack of sterility assurance. This product poses a risk of infection if used. Affected lots: PS2008A, expiring 03/07/2023.
Lack of Assurance of Sterility
Nephron is recalling phenylephrine HCl injection because it may not be sterile. Using this product could lead to infections, especially in medical settings where sterile solutions are critical.
The injection may not be sterile, which can cause infections if used in medical procedures. This is a risk in settings where sterile solutions are critical, such as hospitals or clinics.
Healthcare professionals and patients who have been prescribed this injection. Those using it for medical purposes are most at risk due to potential infection.
Check for the Nephron brand, 50 mg/250 mL phenylephrine HCl injection, and the lot number PS2008A. The expiration date is 03/07/2023.
Look for the lot number PS2008A and expiration date 03/07/2023 on the bottle.
The product may not be sterile, which could lead to infections. Do not use it without confirming it's safe.
Check the lot number and expiration date. If it matches PS2008A and expires 03/07/2023, contact Nephron for guidance.
Check the lot number on the bottle. The recalled product has lot number PS2008A and expires 03/07/2023.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0362-2023 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0362-2023 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.
