Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ibuprofen and Famotidine Tablets 800mg/26.6mg Recalled by Ascend Laboratories, LLC Due to Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate...
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 Ascend Laboratories, LLC directly.
Affected Products
Ibuprofen and Famotidine Tablets 800mg/26.6mg, Rx Only, 90 Tablets per Bottle, manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC., Parsippany, NJ 07054, NDC 67877-626-90
Quantity: 3,288 bottles
Why Was This Recalled?
Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet was discovered in an unopened bottle of Ibuprofen and Famotidine.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ascend Laboratories, LLC
Ascend Laboratories, LLC has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report