Akorn recalls 150mg Rifampin Capsules due to impurities exceeding safety limits. This medication is prescription-only and may pose health risks if used.
Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).
Akorn is recalling 150 mg Rifampin Capsules (30-count bottles) because they contain impurities that exceed safe levels. This could lead to health risks for people taking the medication as prescribed.
The capsules contain impurities that exceed the 5 ppm interim safety limit for 1-Methyl-4-Nitrosopoperazine (MNP). This could potentially cause health issues if the medication is taken as prescribed.
Prescription patients using the recalled Rifampin Capsules. Those with specific medical conditions requiring this medication are at higher risk.
Check for the 150 mg Rifampin Capsules (30-count) with NDC 61748-015-30. Lot numbers 3192818 (exp 10/31/2022), 3199700 (exp 03/31/2023), or 3203853 (exp 02/29/2024).
Look for the NDC code 61748-015-30 and specific lot numbers listed in the recall notice.
The recall states the capsules contain impurities exceeding safety limits, so they are not safe to use as recalled.
Check for the NDC code 61748-015-30 and lot numbers 3192818, 3199700, or 3203853.
The recall does not specify a remedy, so contact your healthcare provider for guidance.
We’ve drafted a message you can send Akorn to request your refund or repair — edit it as you like.
Subject: Recall D-1547-2022 — Akorn Akorn Hello, I own a Akorn that is covered by recall D-1547-2022 from Akorn. 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.
