FDAFDA · Food and drugs·Recall number D-0124-2018
Fluconazole Injection, USP, 2 mg/mL, a) 50 mL (NDC 336000-261-10) and b) 100 mL (NDC 33600-002-10), Rx Only, Manufactured for: Claris LifeSciences, Inc. North Brunswick, NJ 08902 By: Claris Injectables Ltd., Gujarat, India
Published December 27, 2017 · Recall initiated: November 11, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Superpotent
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Renaissance Lakewood, LLC
- Distributor
- Nationwide
- Lot
- a) A060174 01/13/2018, A060257 02/28/2018, A060692 05/31/2018, A061165 09/30/2018, A0A0143 01/31/2019, A0A0347 03/31/2019, and A0A0424 04/30/2019 ; b) A060027 12/31/2017
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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