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

Blood pressure medication recalled: Check your pills

Newsday • 03 nov. 19h23

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

Popular blood pressure tablets face class II recall

WSB-TV • 03 nov. 15h43

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 recalls thousands of blood pressure bottles after it failed quality tests

WGAL • 03 nov. 10h35

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 recalls thousands of blood pressure bottles after it failed quality tests

WCVB • 03 nov. 10h12

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 recalls thousands of blood pressure bottles after it failed quality tests

WMUR • 03 nov. 10h12

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.

Blood pressure medicine recall: Thousands of bottles pulled nationwide

Fox Business • 02 nov. 23h25

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

Thousands of blood pressure medication bottles recalled. See list

USA Today • 02 nov. 18h37

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.

Over 20,000 Bottles of Blood Pressure Medication Recalled Nationwide

Yahoo • 27 oct. 15h10

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.

Over 20,000 Bottles of Blood Pressure Medication Recalled Nationwide

EatingWell • 27 oct. 15h10

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.