Class II Recall

Teva Pharmaceuticals USA

Product
Adenosine Injection, USP, 60mg/20mL (3 mg/mL), 20 mL single-dose vial, Rx only, Manufactured by: Teva Pharmaceuticals USA Inc. Parsippany, NJ 07054, NDC 0703-8776-01
Reason
Lack of Assurance of Sterility
Classification
Class II
Status
Terminated
Lot
Lot #: 100022400, exp. date 04/2023
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
Teva Pharmaceuticals USA — Class II Recall | MedicineWatch US