Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

CLONAZEPAM ORALLY DISINTERGRATING Tablets Recalled by Teva Pharmaceuticals USA, Inc. Due to Failed Content Uniformity Specifications: Recall is being carried...

Date: February 7, 2013
Company: Teva Pharmaceuticals USA, Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Teva Pharmaceuticals USA, Inc. directly.

Affected Products

CLONAZEPAM ORALLY DISINTERGRATING Tablets, USP, 0.5 mg, 60 tablets (10 blister cards of 6 tablets each), TEVA PHARMACEUTICALS USA, Sellersville PA 18960, NDC #0555-0096-96

Quantity: 3 boxes

Why Was This Recalled?

Failed Content Uniformity Specifications: Recall is being carried out due to an out-of-specification result for content uniformity.

Where Was This Sold?

This product was distributed to 1 state: NC

Affected (1 state)Not affected

About Teva Pharmaceuticals USA, Inc.

Teva Pharmaceuticals USA, Inc. has 33 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report