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 Product Mix-up
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/325 mg, 100-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc., Central Islip, NY 11722, NDC 31722-997-01.
Quantity: 9744 bottles
Why Was This Recalled?
Product Mix-up
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