Methylprednisolone Acetate Injectable Suspension USP, 40 mg/mL, 10 mL Multiple Dose Vial, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0703-0045-01
Reported: May 26, 2021 Initiated: April 26, 2021 #D-0376-2021
Product Description
Methylprednisolone Acetate Injectable Suspension USP, 40 mg/mL, 10 mL Multiple Dose Vial, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0703-0045-01
Reason for Recall
Lack of Assurance of Sterility
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 7,564/1 multiple dose vial per carton
- Distribution
- Product was distributed nationwide.
- Location
- Parsippany, NJ
Frequently Asked Questions
What product was recalled? ▼
Methylprednisolone Acetate Injectable Suspension USP, 40 mg/mL, 10 mL Multiple Dose Vial, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0703-0045-01. Recalled by Teva Pharmaceuticals USA. Units affected: 7,564/1 multiple dose vial per carton.
Why was this product recalled? ▼
Lack of Assurance of Sterility
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 26, 2021. Severity: Moderate. Recall number: D-0376-2021.
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