FDA expands Class II recall of blood-pressure tablets to two more lots

Macleods Pharma USA recalls over 3,700 bottles of blood pressure pills

Newsday • 03 Nov 19:23

The FDA classified the recall as Class II after a quality test showed the generic Olmesartan-Amlodipine-Hydrochlorothiazide tablets failed dissolution specifications.

FDA issues Class II recall of two lots of blood pressure tablets

WSB-TV • 03 Nov 15:43

The FDA has classified a recall of two lots of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide tablets as a Class II recall after dissolution failures were identified.

FDA issues nationwide recall of blood pressure medication bottles

WGAL • 03 Nov 10:35

The U.S. Food and Drug Administration has recalled over 3,700 bottles of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide tablets after quality testing showed they did not dissolve properly.

FDA issues nationwide recall of blood pressure medication bottles

WCVB • 03 Nov 10:12

The U.S. Food and Drug Administration has recalled over 3,700 bottles of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide tablets after quality testing showed they did not dissolve properly.

FDA issues nationwide recall of blood pressure medication bottles

WMUR • 03 Nov 10:12

The U.S. Food and Drug Administration has recalled over 3,700 bottles of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide tablets after quality testing showed they did not dissolve properly.

Macleods Pharma USA Recalls Thousands of Blood Pressure Medication Bottles Nationwide

Fox Business • 02 Nov 23:25

Macleods Pharma USA is recalling over 3,700 bottles of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide tablets after the FDA found they failed dissolution testing.

FDA issues Class II recall of thousands of generic blood pressure tablets

USA Today • 02 Nov 18:37

The Food and Drug Administration has classified a recall of over 3,700 bottles of generic blood-pressure medication as Class II, citing failed dissolution specifications that could reduce effectiveness.

FDA Issues Nationwide Recall of Telmisartan and Amlodipine Blood Pressure Pills

Yahoo • 27 Oct 15:10

The U.S. Food and Drug Administration has announced a voluntary Class III recall of more than 21,000 bottles of telmisartan and amlodipine tablets due to potency concerns.

FDA Issues Nationwide Recall of Telmisartan and Amlodipine Bottles

EatingWell • 27 Oct 15:10

The U.S. Food and Drug Administration has announced a voluntary Class III recall of more than 21,000 bottles of telmisartan and amlodipine due to dosage potency issues.