US Drug Recall Register
Class III · Low risk Completed Initiated Jul 2, 2024 (2 years ago)

Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured for…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Cross contamination with other products

What was recalled

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).

Recalling firm
Zydus Pharmaceuticals (USA) Inc
NDC code
16714-301-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0596-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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