Zydus Pharmaceuticals recalls Micafungin 100mg vials due to cross contamination risk. This affects specific lots manufactured for Northstar Rx LLC in Memphis, TN. Patients should contact their healthcare provider for guidance.
Cross contamination with other products
Zydus Pharmaceuticals is recalling Micafungin for injection vials that may have been cross contaminated with other products. This recall affects patients using these specific vials for medical treatment, as cross contamination could lead to unintended medication reactions.
Cross contamination with other products during manufacturing could introduce unintended substances into the medication. This might cause adverse reactions in patients receiving the injection, though the risk is not severe enough to cause serious injury in normal use.
Patients prescribed Micafungin for injection by a healthcare provider in the United States. Those using the specific vial lot numbers mentioned in the recall are most at risk.
Check for the NDC numbers 16714-301-01 (vial) and 16714-301-10 (outer box). The lot number L300217 with expiration date 04/31/2025 is affected. This product was manufactured for Northstar Rx LLC in Memphis, TN.
Patients should contact their healthcare provider to discuss whether they have the recalled vials and what steps to take next.
The recall indicates a potential cross contamination risk, but the product is not considered unsafe for use until the recall is addressed. Patients should follow the recommended actions.
The affected lot number is L300217 with an expiration date of 04/31/2025.
Check the NDC numbers 16714-301-01 (vial) and 16714-301-10 (outer box) on the product packaging. The lot number L300217 is affected.
We’ve drafted a message you can send Zydus Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0596-2024 — Zydus Pharmaceuticals Zydus Pharmaceuticals Hello, I own a Zydus Pharmaceuticals that is covered by recall D-0596-2024 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.
