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    Home»Business»Atorvastatin recall affects over 140,000 cholesterol medication bottles
    Business

    Atorvastatin recall affects over 140,000 cholesterol medication bottles

    adminBy adminOctober 24, 2025No Comments2 Mins Read
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    FDA commissioner Dr. Marty Makary outlines the issues associated with petroleum-based food dyes and the ‘bigger issue’ the agency aims to tackle on ‘The Evening Edit.’

    Federal health officials are advising consumers that more than 140,000 bottles of cholesterol medication are being recalled due to “failed dissolution specifications.”

    Several bottle sizes of Atorvastatin Calcium Tablets, 10-mg (Prescription Only), a medicine used to lower cholesterol and help prevent heart disease, heart attacks and strokes, are impacted by the recall, the Food and Drug Administration (FDA) said in an enforcement report.

    Atorvastatin Calcium Tablets are the generic form of Lipitor and is a medicine from a group called statins. It works by blocking an enzyme in the liver that the body uses to make cholesterol.

    EGG RECALL OVER SALMONELLA CONCERNS EXPANDS

    Atorvastatin Calcium Tablets are the generic form of Lipitor. (George Frey/Bloomberg via Getty Images)

    BEN’S ORIGINAL RICE PRODUCTS RECALLED NATIONWIDE OVER POTENTIAL INJURY RISK

    If a medication has “failed dissolution specifications,” it means the drug did not dissolve in laboratory testing the way it is supposed to according to official standards. If a pill doesn’t dissolve the way it should, the medicine might not work as effectively to control cholesterol levels.

    A pharmacist pulls a drug from a shelf inside a pharmacy in Provo, Utah.

    A pharmacist pulls a drug from a shelf inside a pharmacy in Provo, Utah. (George Frey/Bloomberg via Getty Images)

    SPINACH RECALLED AFTER BATCH TESTS POSITIVE FOR POTENTIALLY HARMFUL BACTERIA 

    A man stands at the pharmacy counter at CVS Pharmacy

    Several bottle sizes of Atorvastatin Calcium Tablets, 10-mg (Prescription Only) are impacted by the recall. (Joe Raedle/Getty Images)

    The alert is considered a Class II recall, which is when the use or exposure to a product “may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote,” according to the FDA’s website.

    GET FOX BUSINESS ON THE GO BY CLICKING HERE

    The medication was manufactured by Alkem Laboratories and distributed by Ascend Laboratories LLC.

    There are eight lot numbers impacted with expiration dates ranging between July 2026 to February 2027. The bottle sizes included 90 tablets, 500 tablets and 1,000 tablets.

    FOX Business reached out to Alkem Laboratories and Ascend Laboratories for comment.



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