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).
Reported: July 17, 2024 Initiated: July 2, 2024 #D-0596-2024
Product Description
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).
Reason for Recall
Cross contamination with other products
Details
- Recalling Firm
- Zydus Pharmaceuticals (USA) Inc
- Units Affected
- n/a
- Distribution
- Nationwide in the USA and Puerto Rico
- Location
- Pennington, NJ
Frequently Asked Questions
What product 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).. Recalled by Zydus Pharmaceuticals (USA) Inc. Units affected: n/a.
Why was this product recalled? ▼
Cross contamination with other products
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 17, 2024. Severity: Low. Recall number: D-0596-2024.
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