Lupin Pharmaceuticals recalls 300mg Rifampin Capsules USP 30-count bottles due to subpotent drug content. This may not provide intended treatment. Contact for details.
Subpotent Drug
Lupin Pharmaceuticals is recalling 300mg Rifampin Capsules USP 30-count bottles because they contain less active drug than intended. This could lead to treatment failure if used as prescribed.
The capsules contain less active drug than labeled, meaning they may not provide the intended treatment effect. This could lead to treatment failure for conditions requiring Rifampin, such as tuberculosis. The risk is not immediate harm but potential ineffective treatment.
Prescription patients who have received this specific bottle of Rifampin Capsules USP 300mg 30-count. Patients using the medication for infections like tuberculosis are most at risk.
Check for the product name 'Rifampin Capsules USP', strength 300mg, 30-count bottles, and the lot number A201064 with expiration date March 2024. The product is prescription-only and manufactured by Lupin Pharmaceuticals Inc.
Verify the product name, strength, count, and lot number to confirm if it matches the recalled items.
The capsules contain less active drug than intended, which could lead to treatment failure for conditions like tuberculosis.
No serious injury risk is described; the hazard is treatment failure due to subpotent drug content.
The recall record does not specify a remedy, so check with your healthcare provider or contact Lupin Pharmaceuticals for guidance.
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0437-2024 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-0437-2024 from Lupin Pharmaceuticals. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
