Ascend Laboratories, LLC: Drug Recall

Recall #D-0019-2026 · 09/19/2025

Class II: Risk

Recall Details

Recall Number
D-0019-2026
Classification
Class II
Product Type
Drug
Recalling Firm
Ascend Laboratories, LLC
Status
Ongoing
Date Initiated
09/19/2025
Location
Bedminster, NJ, United States
Voluntary/Mandated
Voluntary: Firm initiated

Reason for Recall

Failed Dissolution Specifications

Product Description

Atorvastatin Calcium Tablets USP, 20 mg, Rx Only, a). 90-count(NDC 67877-512-90), b). 500-count (NDC 67877-512-05), c). 1000-count(NDC 67877-512-10),Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054.

Distribution Pattern

U.S. Nationwide

Other Recalls by Ascend Laboratories, LLC

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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.