PlainRecalls
FDA Drug Moderate Class II Ongoing

Atorvastatin Calcium Tablets USP, 80 mg, Rx Only, a). 90-count(NDC 67877-514-90), b). 500-count(NDC 67877-514-05), Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054

Reported: October 22, 2025 Initiated: September 19, 2025 #D-0020-2026

Product Description

Atorvastatin Calcium Tablets USP, 80 mg, Rx Only, a). 90-count(NDC 67877-514-90), b). 500-count(NDC 67877-514-05), Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054

Reason for Recall

Failed Dissolution Specifications

Details

Recalling Firm
Ascend Laboratories, LLC
Distribution
U.S. Nationwide
Location
Bedminster, NJ

Frequently Asked Questions

What product was recalled?
Atorvastatin Calcium Tablets USP, 80 mg, Rx Only, a). 90-count(NDC 67877-514-90), b). 500-count(NDC 67877-514-05), Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. Recalled by Ascend Laboratories, LLC.
Why was this product recalled?
Failed Dissolution Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on October 22, 2025. Severity: Moderate. Recall number: D-0020-2026.