Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL Laboratories) Due to Failed Impurities/Degradation Specifications: out of specification result for...
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 Mylan Institutional, Inc. (d.b.a. UDL Laboratories) directly.
Affected Products
Clonazepam Tablets, USP, 0.5 mg, 100-count carton, Rx only, Manufactured by Mylan Pharmaceuticals Inc., Morgantown, WV, 26505, NDC:51079-881-21
Quantity: 868 unit cartons (86,800 tablets)
Why Was This Recalled?
Failed Impurities/Degradation Specifications: out of specification result for known impurity at 6 month timepoint.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mylan Institutional, Inc. (d.b.a. UDL Laboratories)
Mylan Institutional, Inc. (d.b.a. UDL Laboratories) has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report