Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Contrave (naltrexone HCl and bupropion HCl) Extended-Release Tablets Recalled by Orexigen Therapeutics, Inc. Due to Defective Container: Customer complaints of punctures in the...
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 Orexigen Therapeutics, Inc. directly.
Affected Products
Contrave (naltrexone HCl and bupropion HCl) Extended-Release Tablets, 8 mg/90 mg, 120-count bottle, Rx only, Distributed by Orexigen therapeutics, Inc., La Jolla, CA 92037, NDC 51267-890-99.
Quantity: 95,296 bottles
Why Was This Recalled?
Defective Container: Customer complaints of punctures in the bottle.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Orexigen Therapeutics, Inc.
Orexigen Therapeutics, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report