FDA Drug · D-0556-2026

Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, Rx Only, 30-count bottle, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascend Laboratories, LLC., Parsippany, NJ 07054, NDC 67877-501-30.

Class II · Ongoing

Failed Dissolution Specifications: Olmesartan Medoxomil content below specifications

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Affected lots / codes — check yours against thisLot: 24123460, Expires: October 31, 2027.
Recalling firm
Ascend Laboratories, LLC, Bedminster, NJ
Classification
Class II (temporary or reversible harm possible)
Status
Ongoing
Quantity
15,696 x 30's bottles
Distribution
U.S.A. Nationwide
Recall initiated
May 5, 2026
Classified
June 2, 2026
Initiation
Voluntary: Firm initiated
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Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0556-2026%22
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Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.
Check this brand across all 8 databases →