FDAFDA · Food and drugs·Recall number D-0596-2024
Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Zydus Lifesciences Ltd., Vadodara, India, NDC 16714-301-01 (vial), NDC 16714-301-10 (outer box).
Published July 17, 2024 · Recall initiated: July 2, 2024
Status when published: Completed — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Cross contamination with other products
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Zydus Pharmaceuticals (USA) Inc
- Distributor
- Nationwide in the USA and Puerto Rico
- Lot
- Lot #: L300217, Exp. 04/31/2025.
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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