{"id":892035,"date":"2026-06-25T15:27:17","date_gmt":"2026-06-25T15:27:17","guid":{"rendered":"https:\/\/www.europesays.com\/us\/892035\/"},"modified":"2026-06-25T15:27:17","modified_gmt":"2026-06-25T15:27:17","slug":"11400-bottles-of-blood-pressure-medication-recalled-nationwide-fda-reports","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/us\/892035\/","title":{"rendered":"11,400 Bottles of Blood Pressure Medication Recalled Nationwide, FDA Reports"},"content":{"rendered":"

\"Estimated2 min read<\/p>\n

Over 11,0000 bottles of the blood pressure medication chlorthalidone have been recalled nationwide, according to the Food and Drug Administration (FDA<\/a>). The FDA classified this as a Class II recall, meaning that exposure to the product may cause temporary or medically reversible adverse health consequences.<\/p>\n

The agency reports the tablets were recalled by their manufacturer, Inventia Healthcare Limited, because they \u201cfailed dissolution specifications.\u201d Dissolution is a pharmaceutical term that describes how a medication dissolves and releases into the body, which affects how well it works to treat a condition. An issue with dissolution, therefore, could directly impact a medication\u2019s efficacy.<\/p>\n

Chlorthalidone is a diuretic, meaning it decreases the amount of water in the body by increasing urination. It\u2019s commonly used to treat high blood pressure, according to the Mayo Clinic<\/a>, but may also be used to treat edema or fluid retention.<\/p>\n

If you take chlorthalidone, it\u2019s worth checking if your bottle is included in the recall.<\/p>\n

How to tell if your medication is included in the recall<\/p>\n

The recall includes 25mg tablets of chlorthalidone, which were distributed in bottles containing either 100 or 1,000 tablets. Check the information below against the label on your bottle:<\/p>\n

100-tablet bottle:<\/strong><\/p>\n