RecallRadar

FDA Drug recall D-0556-2026

Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, Rx Only, 30-count bottle, Manufactured by: Alkem Laboratories Ltd., India, Distribut…

On 2026-06-10 the FDA classified a Class II recall of Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, Rx Only, 30-count bottle, Manufactured by: Alkem Laboratories Ltd., India, Distribut… by Ascend Laboratories, citing failed Dissolution Specifications: Olmesartan Medoxomil content below specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0556-2026
ClassificationClass II
Statusongoing
Initiated2026-05-05
Published2026-06-10
Last updated2026-09-13 11:52 UTC
CompanyAscend Laboratories
DistributionUS

Product

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.

Reason

Failed Dissolution Specifications: Olmesartan Medoxomil content below specifications

Identifiers

ndc67877-499-30
ndc67877-499-90
ndc67877-500-30
ndc67877-500-90
ndc67877-501-30
ndc67877-501-90
ndc67877-502-30
ndc67877-502-90
code_infoLot: 24123460, Expires: October 31, 2027.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0556-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.