Sun Pharmaceutical recalls Amphotericin B Liposome injections due to subpotent drug levels. This may reduce effectiveness for serious fungal infections. Patients with prescribed treatment should contact their doctor.
Subpotent drug
Sun Pharmaceutical is recalling Amphotericin B Liposome injections because they may be subpotent, meaning they don't contain enough active drug to treat fungal infections effectively. This could lead to treatment failure if the medication isn't strong enough.
The drug may be subpotent, meaning it contains less active ingredient than intended. This could result in the medication not working well enough to treat serious fungal infections, potentially leading to treatment failure.
Patients prescribed Amphotericin B Liposome injections for serious fungal infections. Those with the specific lot numbers BAD0089A (expiring Jan 2025) or BAD0330A (expiring July 2025) are most at risk.
Check the product label for the NDC code 62756-0233-01. Look for lot numbers BAD0089A (expiring Jan 2025) or BAD0330A (expiring July 2025).
Look for the NDC code 62756-0233-01 and lot numbers BAD0089A or BAD0330A on the product label.
The product may be subpotent, meaning it could be less effective than intended. Patients should not use it without consulting their doctor.
Check the product label for the NDC code 62756-0233-01 and lot numbers BAD0089A or BAD0330A. If you have these, contact your doctor for guidance.
The product expires in January 2025 for lot BAD0089A and July 2025 for lot BAD0330A.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-0891-2023 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-0891-2023 from Sun Pharmaceutical. 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.
