{"id":7992,"date":"2026-11-03T00:11:28","date_gmt":"2026-11-03T00:11:28","guid":{"rendered":"https:\/\/www.vaultinsider.top\/?p=7992"},"modified":"2026-11-03T00:11:28","modified_gmt":"2026-11-03T00:11:28","slug":"blood-pressure-medicine-recall-thousands-of-bottles-pulled-nationwide","status":"publish","type":"post","link":"https:\/\/www.vaultinsider.top\/?p=7992","title":{"rendered":"Blood pressure medicine recall: Thousands of bottles pulled nationwide"},"content":{"rendered":"
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Assistant to President Donald Trump Jarrod Agen discusses the administration\u2019s energy policies and the president\u2019s efforts to rally voters ahead of Election Day on \u2018The Evening Edit.\u2019<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n
Americans who take medication for high blood pressure may want to check their medicine cabinets after thousands of bottles of a prescription drug were recalled nationwide.<\/p>\n
New Jersey-based Macleods Pharma USA is recalling certain lots of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Tablets after the medication failed to meet federal quality standards, according to the U.S. Food and Drug Administration (FDA).<\/p>\n
The recall covers 3,528 30-count bottles from lot 12251163A and 216 90-count bottles from lot 12251163B. Both lots expire May 31, 2027.<\/p>\n
NEARLY 6 MILLION COFFEE MAKERS SOLD AT MAJOR RETAILERS RECALLED OVER BURN RISK<\/strong><\/p>\n
Americans who take medication for high blood pressure may want to check their medicine cabinets after thousands of bottles of a prescription drug were recalled nationwide.<\/span> (iStock)<\/span><\/p>\n<\/div>\n<\/div>\n
Consumers can check their prescription bottles for the lot number and National Drug Code, or NDC. The recalled 30-count bottles have NDC 33342-246-07, while the 90-count bottles have NDC 33342-246-10.<\/p>\n
The FDA listed the reason for the recall as “failed dissolution specifications,” meaning the pills did not dissolve as required during testing.<\/p>\n
POPULAR KIDS’ TOOTHPASTES AMONG 4M TUBES RECALLED NATIONWIDE<\/strong><\/p>\n
The FDA listed the reason for the recall as “failed dissolution specifications.”<\/span> (iStock)<\/span><\/p>\n<\/div>\n<\/div>\n
The agency classified the action as a Class II recall, meaning use of the affected medication “may cause temporary or medically reversible adverse health consequences” but the likelihood of serious health consequences is considered remote.<\/p>\n
Macleods Pharma USA initiated the recall Oct. 7, and the FDA classified it Oct. 26. The recall remains ongoing and affects products distributed nationwide.<\/p>\n
The recall comes weeks after another blood pressure medication was pulled from shelves over a similar issue.<\/p>\n
HYUNDAI RECALLS MORE THAN 94,000 VEHICLES OVER FIRE RISK<\/strong><\/p>\n
The recall comes weeks after another blood pressure medication was pulled from shelves over a similar issue.<\/span> (iStock)<\/span><\/p>\n<\/div>\n<\/div>\n
India-based Inventia Healthcare Ltd. recalled 13,567 bottles of 25-milligram chlorthalidone tablets in September after the medication failed dissolution testing, according to the FDA.<\/p>\n
CLICK HERE TO GET FOX BUSINESS ON THE GO<\/u><\/strong><\/p>\n
Chlorthalidone is used to treat high blood pressure and fluid retention, according to Mayo Clinic.<\/p>\n
Macleods Pharma USA could not immediately be reached by FOX Business for comment.<\/p>\n
FOX Business’ Matthew Kazin contributed to this report.<\/i><\/p>\n<\/div>\n
Assistant to President Donald … <\/p>\n","protected":false},"author":1,"featured_media":7993,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[2],"tags":[2814,4574,8265,697,532,10134,954,3204],"class_list":["post-7992","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-finance-news","tag-blood","tag-bottles","tag-medicine","tag-nationwide","tag-pressure","tag-pulled","tag-recall","tag-thousands"],"yoast_head":"\n
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