Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Vaseretic (enalapril maleate/hydrochlorothiazide) 10/25 mg Tablets Recalled by Valeant Pharmaceuticals North America LLC Due to Labeling: Incorrect or Missing Package Insert: Product is...
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 Valeant Pharmaceuticals North America LLC directly.
Affected Products
Vaseretic (enalapril maleate/hydrochlorothiazide) 10/25 mg Tablets, NDC 0187-0146-01, 100 ct. bottles manufactured at Valeant Pharmaceuticals International, Inc., Steinbach, MD R5G 1Z7 Canada
Quantity: 205,853 bottles
Why Was This Recalled?
Labeling: Incorrect or Missing Package Insert: Product is packaged with the incorrect version of the package outset
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Valeant Pharmaceuticals North America LLC
Valeant Pharmaceuticals North America LLC has 25 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report