Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
SECONAL SODIUM (secobarbital sodium) Capsules Recalled by Valeant Pharmaceuticals North America LLC Due to Labeling: Incorrect or Missing Package Insert: Package insert...
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
SECONAL SODIUM (secobarbital sodium) Capsules, USP, 100 mg, 100 Ct. Bottles, Rx Only. Distributed by: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ 08807. NDC: 0187-4220-10.
Quantity: 958 Bottles
Why Was This Recalled?
Labeling: Incorrect or Missing Package Insert: Package insert is missing warning regarding anaphylaxis.
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