Nephron recalls Neostigmine Methylsulfate injections due to lack of sterility assurance. This affects specific lots and expiration dates. Patients should contact their healthcare provider for guidance.
Lack of Assurance of Sterility
Nephron is recalling Neostigmine Methylsulfate injections because they may not be sterile. This could lead to infections if used improperly. Patients should not use these products and contact their doctor for alternatives.
The injections may not be sterile, which can cause infections if used. This is a serious risk for patients who need the medication for medical conditions.
Patients prescribed Neostigmine Methylsulfate injections by a healthcare provider. Those with specific lot numbers and expiration dates listed in the recall are most at risk.
Check the product label for the lot numbers NE2004A, NE2010A, or NE2013A with expiration dates 7/26/2022, 9/5/2022, or 10/20/2022. The product is only available by prescription.
Discard the recalled injections if you have them.
The recall states there is a lack of sterility assurance, so it is not safe to use.
Discard the product and contact your healthcare provider for alternatives.
Check the lot numbers NE2004A, NE2010A, or NE2013A with specific expiration dates 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-1271-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1271-2022 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.