Nephron recalls 5x5mL Neostigmine injections due to potential contamination risks. Products with lots NE2001A or NE2009B may be unsafe. Check your NDC code for affected items.
Lack of Assurance of Sterility
Nephron is recalling certain Neostigmine injections because they may not be sterile, which could lead to infections. This is serious for patients using the medication.
The injections lack proper sterility assurance, meaning they could contain harmful bacteria or other contaminants. This poses a risk of infection or serious health complications if used.
Patients prescribed Neostigmine injections by a doctor. Those using the recalled product without medical supervision are at highest risk.
Check for NDC code 69374-902-05 on the packaging. Look for lots NE2001A (expiring 6/30/2022) or NE2009B (expiring 8/27/2022).
Immediately discard any recalled Neostigmine injections with lots NE2001A or NE2009B.
No, the recalled injections lack sterility assurance and could cause infections. Do not use.
The NDC code is 69374-902-05.
Check the NDC code on the packaging. If it's 69374-902-05 and the lot number is NE2001A or NE2009B, it's affected.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0963-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0963-2022 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.
