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

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

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On November 3, the U. S. Food and Drug Administration classified a recall of two lots of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide tablets as Class II after dissolution failures were identified, WSB-TV reported.

The recall covers the same generic blood-pressure medication previously withdrawn. The agency had earlier, on October 26, issued a Class II recall of more than 3,700 bottles of the same three-component tablets after quality testing showed they did not dissolve properly, according to USA Today and WMUR. A separate voluntary Class III recall of over 21,000 bottles of telmisartan-amlodipine tablets was announced because of potency concerns, Yahoo reported.

अभिनेताओं

U.S. Food and Drug Administration Mylan Pharmaceuticals

स्थान

United States

लेख

03 नवंबर 2026
5 कुल
Blood pressure medication recalled: Check your pills
Blood pressure medication recalled: Check your pills

Newsday • 03 नवं 19:23

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

विश्वसनीयता 92% हेरफेर 5% मध्यस्थ
Popular blood pressure tablets face class II recall
Popular blood pressure tablets face class II recall

WSB-TV • 03 नवं 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.

विश्वसनीयता 88% हेरफेर 5% मध्यस्थ
FDA recalls thousands of blood pressure bottles after it failed quality tests
FDA recalls thousands of blood pressure bottles after it failed quality tests

WGAL • 03 नवं 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.

विश्वसनीयता 92% हेरफेर 5% मध्यस्थ
FDA recalls thousands of blood pressure bottles after it failed quality tests
FDA recalls thousands of blood pressure bottles after it failed quality tests

WCVB • 03 नवं 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.

विश्वसनीयता 92% हेरफेर 5% मध्यस्थ
FDA recalls thousands of blood pressure bottles after it failed quality tests
FDA recalls thousands of blood pressure bottles after it failed quality tests

WMUR • 03 नवं 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.

विश्वसनीयता 92% हेरफेर 5% मध्यस्थ
02 नवंबर 2026
2 कुल
Blood pressure medicine recall: Thousands of bottles pulled nationwide
Blood pressure medicine recall: Thousands of bottles pulled nationwide

Fox Business • 02 नवं 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.

विश्वसनीयता 92% हेरफेर 8% मध्यस्थ
Thousands of blood pressure medication bottles recalled. See list
Thousands of blood pressure medication bottles recalled. See list

USA Today • 02 नवं 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.

विश्वसनीयता 92% हेरफेर 5% मध्यस्थ
27 अक्टूबर 2026
2 कुल
Over 20,000 Bottles of Blood Pressure Medication Recalled Nationwide
Over 20,000 Bottles of Blood Pressure Medication Recalled Nationwide

Yahoo • 27 अक्टू 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.

विश्वसनीयता 78% हेरफेर 8% मध्यस्थ
Over 20,000 Bottles of Blood Pressure Medication Recalled Nationwide
Over 20,000 Bottles of Blood Pressure Medication Recalled Nationwide

EatingWell • 27 अक्टू 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.

विश्वसनीयता 72% हेरफेर 8% मध्यस्थ

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