FDA recall D-0596-2024

Product

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

Distribution

Nationwide in the USA and Puerto Rico

Key facts

Status

Completed

Initiation date

2024-07-02

Report date

2024-07-17

Voluntary/Mandated

Voluntary: Firm initiated

Location

Pennington, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0596-2024