FDAFDA · Food and drugs·Recall number D-1094-2017
Voriconazole Tablets, 200 mg, 20-count cartons (4 x 5) Unit Dose, Rx only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 50268-804-12
Published August 23, 2017 · Recall initiated: July 19, 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
Failed impurities/degradation specifications: Out of specification for a related compound C.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- AVKARE Inc.
- Distributor
- Nationwide
- Lot
- Lot #: 16933, Exp 07/2018; 17054, Exp 08/2018
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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