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Moderate riskFDA DrugClass II

Teva metoprolol succinate tablets recalled for failed dissolution

Teva Pharmaceuticals is recalling specific lots of metoprolol succinate extended-release 200 mg tablets because they failed to meet dissolution specifications—meaning the tablets may not break down and release the medication properly in your body. This could affect how well the blood pressure medication works. No injuries have been reported.

From the FDA notice · Read the official notice ↗ · All Teva recalls

What to do

  1. Check if your metoprolol succinate 200 mg bottle matches lot numbers 0686H251, 0687H251, or 10688H251 with expiration 02/2027 (NDC 45963-678-11)
  2. If you have an affected bottle, contact your pharmacy or doctor before stopping the medication
  3. Do not stop taking your blood pressure medication without medical guidance
  4. Return the recalled bottle to your pharmacy
Official notice ↗

Is yours affected?

Compare your label or packaging with the recalled product.

Product
Metoprolol Succinate Extended-Release Tablets, 200 mg, 100 tablets bottles, Rx Only, Teva Pharmaceuticals, Parsippany, NJ 07054, NDC: 45963-678-11
Sold in
Nationwide
Made for
Adults (0 months and older)

This recall covers 4 products — see all of them.

Details

Units affected
19,056 bottles
Illnesses reported
None reported
Manufactured in
400 Interpace Pkwy Bldg A, N/A, Parsippany, NJ, United States
Classification
Class II
Recall number
D-0357-2026

In the FDA's words

Description
Metoprolol Succinate Extended-Release Tablets, 200 mg, 100 tablets bottles, Rx Only, Teva Pharmaceuticals, Parsippany, NJ 07054, NDC: 45963-678-11 Failed Dissolution Specifications Lot#: a) 0686H251, 0687H251, 10688H251, Exp.: 02/2027. . Distribution: Nationwide Affected quantity: 19,056 bottles
Hazard
Failed Dissolution Specifications

4 products in this recall

Teva metoprolol succinate tablets recalled for dissolution failure

Teva is recalling four strengths of metoprolol succinate extended-release tablets (25 mg, 50 mg, 100 mg and 200 mg), sold in 100- and 1,000-tablet bottles. The tablets did not meet the required dissolution specification, which means they may not release the medicine at the expected rate. No injuries have been reported.

The agency lists each product separately. Check every one you might have.

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