Zydus Pharmaceuticals (USA) Inc recalls Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN…
- Recall date
- July 2, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0596-2024
- FDA classification
- Class III
- Brand / firm
- Zydus Pharmaceuticals (USA) Inc
- Sold / distributed
- Nationwide in the USA and Puerto Rico
Why it was recalled
Cross contamination with other products
Class III means the product violates regulations but is not likely to cause harm.
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).
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