Zydus Pharmaceuticals recalls Micafungin 100mg vials due to cross contamination risk. This affects prescription-only injectable medication manufactured in India and distributed in the US. No specific remedy is listed in the recall notice.
Cross contamination with other products
Zydus Pharmaceuticals is recalling Micafungin for injection (100 mg/vial) because of cross contamination with other products. This recall affects prescription-only medication that could pose a risk to patients using the product.
Cross contamination with other products during manufacturing could introduce harmful substances into the medication. This may lead to adverse reactions or infections in patients receiving the injection.
Prescription patients using Micafungin for injection, 100 mg/vial, single-dose vials. Patients who have received this medication from the recalled lot numbers are most at risk.
Check for the NDC 70710-1725-01 (vial) or NDC 70710-1725-06 (outer box) on the product. The lot number L300220 with expiration date 05/31/2025 is affected.
Look for NDC 70710-1725-01 (vial) or NDC 70710-1725-06 (outer box) and lot number L300220 on the product.
The recall notice states there is a risk of cross contamination, but no specific remedy is provided. Patients should check if they have the recalled lot number.
The recall notice does not specify any action steps. Check the product details to see if it matches the recalled items.
Check for NDC 70710-1725-01 (vial) or NDC 70710-1725-06 (outer box) and lot number L300220 on the product.
We’ve drafted a message you can send Zydus Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0595-2024 — Zydus Pharmaceuticals Zydus Pharmaceuticals Hello, I own a Zydus Pharmaceuticals that is covered by recall D-0595-2024 from Zydus 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.
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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.
