Teva Pharmaceuticals is recalling 18,780 bottles of Metoprolol Succinate Extended-Release Tablets, 25 mg, distributed nationwide. The recall is due to failed dissolution specifications that could affect dosing. Patients should stop using affected bottles and contact Teva or their healthcare provider for guidance.
Failed Dissolution Specifications
Consumers and healthcare providers should stop using this product immediately. Contact Teva Pharmaceuticals USA, Inc or your healthcare provider for guidance. Notification method: Letter
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Product: Metoprolol Succinate Extended-Release Tablets, 25 mg. NDCs: 45963-709-11 (100-tablet bottles) and 45963-709-96 (1000-tablet bottles). Quantity recalled: 18,780 bottles. Manufacturer: Teva Pharmaceuticals USA, Parsippany, NJ 07054. Sold nationwide as Rx-only.
The product failed dissolution specifications. This can cause inconsistent drug release and suboptimal blood pressure and heart rate control.
1. Stop using the product. 2. Contact Teva Pharmaceuticals USA, Inc or your healthcare provider for guidance.
Official recall page: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0354-2026. Additional contact details were not provided in the notice.
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