FDAFDA · Food and drugs·Recall number D-1302-2020
oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV Use, Rx only, QuVa Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 888-339-0874, NDC 70092-1068-07
Published June 17, 2020 · Recall initiated: May 28, 2020
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
Subpotent drug - Product did not contain drug.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- QuVa Pharma, Inc.
- Distributor
- USA Nationwide
- Lot
- Lot#: 30010515
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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