Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Clonazepam Tablets Recalled by Actavis Elizabeth LLC Due to Subpotent Drug: During routine stability testing one tablet...
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 Actavis Elizabeth LLC directly.
Affected Products
Clonazepam Tablets, USP 2 mg 100 tablets Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue, Elizabeth, NJ 0737 USA NDC 0228-3005-11 packaged in White/Round HDPE 75 CC with white/round plastic 33 mm CRC closure shipped in corrugated 75 cc carton (24 bottles/carton)
Quantity: 13,608 bottles
Why Was This Recalled?
Subpotent Drug: During routine stability testing one tablet was found with tablet weight below specification.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Actavis Elizabeth LLC
Actavis Elizabeth LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report