Nephron recalls Neostigmine Methylsulfate injections due to potential lack of sterility. This could cause infections if used. Patients should contact their healthcare provider for guidance.
Lack of Assurance of Sterility
Nephron is recalling Neostigmine Methylsulfate injections that may not be sterile. Using these injections could lead to infections, especially in medical treatments.
The injections may not be sterile, which could lead to infections if used. This is a risk for patients receiving the medication for medical conditions like myasthenia gravis.
Patients prescribed Neostigmine Methylsulfate injections by a healthcare provider. Those with the specific lot numbers and expiration dates listed are most at risk.
Check for the product name 'Neostigmine Methylsulfate Injection, USP, 3 mg/3 mL (1 mg/mL) syringe' in 5 x 3 mL Pre-Filled Syringes per carton. Look for lot numbers NE2002A through NE2012D with specific expiration dates.
Talk to your doctor or pharmacist about the recalled product and possible alternatives.
The recall states there is a lack of assurance of sterility, which could lead to infections. Do not use the product without consulting your healthcare provider.
Lot numbers NE2002A, NE2003A, NE2006A, NE2007A, NE2008A, NE2009A, and NE2012D with specific expiration dates.
Check the product label for the lot numbers and expiration dates listed in the recall notice.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1270-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1270-2022 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.