FDAFDA · Food and drugs·Recall number D-0371-2022
Norepinephrine Bitartrate Injection USP 4 mg/4 mL (1 mg/mL), 4 mL Single-Dose Vials, 10 vials per carton, Rx Only, Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0703-1153-03.
Published January 19, 2022 · Recall initiated: December 31, 2021
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
Lack of Assurance of Sterility
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Teva Pharmaceuticals USA
- Distributor
- Methylprednisolone, TN Norepinephrine BItartrate - MS, OH
- Lot
- Lot # 100020800, exp 07/2022
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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