Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Ascent Pharmaceuticals, Inc. Due to Presence of Foreign Tablet/Capsule: One bottle of Hydrocodone...
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 Ascent Pharmaceuticals, Inc. directly.
Affected Products
Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc. Central Islip, NY 11722, NDC 31722-943-01
Quantity: 9768 Bottles
Why Was This Recalled?
Presence of Foreign Tablet/Capsule: One bottle of Hydrocodone Bitartrate and Acetaminophen Tablets USP 10mg/325 mg contains one Losartan Potassium Tablets, USP 100 mg.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ascent Pharmaceuticals, Inc.
Ascent Pharmaceuticals, Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report