Ascent Pharmaceuticals, Inc.: Drug Recall
Recall #D-0276-2022 · 11/19/2021
Class II: Risk
Recall Details
- Recall Number
- D-0276-2022
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Ascent Pharmaceuticals, Inc.
- Status
- Terminated
- Date Initiated
- 11/19/2021
- Location
- Central Islip, NY, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9744 bottles
Reason for Recall
Product Mix-up
Product Description
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.
Distribution Pattern
USA Nationwide
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.