MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 16714-090-01, packaged in cartons.
Reported: January 19, 2022 Initiated: December 31, 2021 #D-0370-2022
Product Description
MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 16714-090-01, packaged in cartons.
Reason for Recall
Lack of Assurance of Sterility
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 7,400 cartons
- Distribution
- Methylprednisolone, TN Norepinephrine BItartrate - MS, OH
- Location
- Parsippany, NJ
Frequently Asked Questions
What product was recalled? ▼
MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 16714-090-01, packaged in cartons.. Recalled by Teva Pharmaceuticals USA. Units affected: 7,400 cartons.
Why was this product recalled? ▼
Lack of Assurance of Sterility
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 19, 2022. Severity: Moderate. Recall number: D-0370-2022.
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