Zydus Pharmaceuticals (USA) Inc 2024-07-17 Health moderate FDA
Health · FDA · Recall #FDA-D-0595-2024
Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured by:… Recall
Issued July 17, 2024 · Zydus Pharmaceuticals (USA) Inc
In July 2024, Zydus Pharmaceuticals (USA) Inc recalled the Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured by:…, a moderate health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Cross contamination with other products
What you should do
- 1 Stop using Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured by:… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Zydus Pharmaceuticals (USA) Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Zydus Pharmaceuticals (USA) Inc
- Category
- Health
- Recall date
- July 17, 2024
- Units affected
- Not reported
- Sold at
- Nationwide in the USA and Puerto Rico
- Recall number
- FDA-D-0595-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Zydus Pharmaceuticals (USA) Inc has 31 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.