Class II

Drug Recall: Amlodipine and Olmesartan Medoxomil Tablets, 10 mg/20 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC., Parsnippany, NJ 07

Ascend Laboratories, LLC · July 8, 2026

Reason for Recall

Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications

Product Description

Amlodipine and Olmesartan Medoxomil Tablets, 10 mg/20 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC., Parsnippany, NJ 07054. NDC: 67877-500-30

Distribution

Nationwide in the USA

States Affected

NATIONWIDE

Quantity Affected

6,192 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0712-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.