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Yeshiva World News · Nov 3, 2026

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A New Jersey drug maker is recalling 3,744 bottles of a combination blood pressure medication after the tablets failed an FDA dissolution test. The Class II recall covers certain lots of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide tablets expiring May 31, 2027; the FDA says the risk of serious harm is remote.

A New Jersey drug maker is recalling 3,744 bottles of a combination blood pressure medication after the tablets failed an FDA dissolution test. The Class II recall covers certain lots of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide tablets expiring May 31, 2027; the FDA says the risk of serious harm is remote.

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