Tag: fda

  • FDA upgrades recall of frozen blueberries sold at Publix to highest health risk level | Thousands…

    FDA upgrades recall of frozen blueberries sold at Publix to highest health risk level | Thousands…

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    FDA upgrades recall of frozen blueberries sold at Publix to highest health risk level

    The Food and Drug Administration upgraded a recall of frozen blueberries and mixed berries sold at Publix grocery stores across the U.S. to the highest health risk level on Tuesday, according to an enforcement report. 

    Publix on July 29 announced a recall of four varieties of frozen GreenWise organic blueberries and mixed berries sold at stores across eight states over potential E. coli contamination. The FDA is now categorizing it as a "Class 1" recall, which the agency assigns to product recalls "in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death."

    Thousands of blueberries recalled as FDA issues highest risk warning

    A series of frozen blueberry and mixed berry products that were recalled due to possible E. coli contamination have been issued the highest risk warning by the U.S. Food and Drug Administration (FDA).

    The Class I risk classification, issued on Tuesday, applies to four GreenWise products sold at Publix:

    A Class I risk classification—one of three—represents "a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death," according to the FDA.

    Publix recalled all lots of the products on July 29 because they may have been contaminated with E. coli O145, a strain that can cause severe stomach cramps, diarrhea, and vomiting.

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  • FDA recalls levothyroxine sodium tablets. Here’s what to know | Nationwide recall issued for this…

    FDA recalls levothyroxine sodium tablets. Here’s what to know | Nationwide recall issued for this…

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    FDA recalls levothyroxine sodium tablets. Here's what to know

    Recalls occur when manufacturers and distributors remove products “that present a risk of injury or gross deception or are otherwise defective,” according to the FDA.

    The Food and Drug Administration has recalled a commonly prescribed thyroid medication.

    The recall involves levothyroxine sodium tablets that are used to treat hypothyroidism and decrease the size of enlarged thyroid glands, according to Mayo Clinic.

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    The FDA said they had been functioning as "subpotent drugs," meaning they had less of an active ingredient and were ultimately less effective.

    Major Pharmaceuticals packaged and distributed the recalled tablets, while Cardinal Health also distributed some of the recalled products.

    Nationwide recall issued for this thyroid medication. See products

    Major Rugby, a pharmaceutical manufacturer that produces levothyroxine sodium tablets, issued a nationwide recall for the common thyroid medication, according to a letter it sent to retailers earlier this month.

    While consumers are being urged to return their medicine to the point of purchase, Major Rugby said in its letter that taking them "is not likely to cause adverse health effects."

    Here’s what you should know about the recalled products and how to identify them.

    Major Rugby issued a recall for 12 of its levothyroxine sodium tablet packages, including individual packs of 10 and boxes containing 10 blister packs.

    The Mayo Clinic notes that levothyroxine sodium tablets are used to treat hypothyroidism, enlarged thyroid glands and a type of thyroid cancer.

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  • FDA Announces Recall of Common Blood Pressure Medication | Over 11,000 bottles of blood pressure …

    FDA Announces Recall of Common Blood Pressure Medication | Over 11,000 bottles of blood pressure …

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    Over 11,000 bottles of blood pressure medicine recalled across the U.S.

    A common blood pressure medicine has been recalled across the country. The Food and Drug Administration has recalled more than 11,000 bottles of a Chlorthalidone.

    The recall is for 11,460 bottles of Chlorthalidone tablets, USP, 25 milligrams. The drug failed to meet the FDA regulation for dissolvability. If the drug does not dissolve properly it could lead to incorrect dosages, less effective or ineffective medication. 

    The recall impacts 100 tablet and 1,000 tablet bottles with an expiration date of April 2027 and have the following batch numbers:

    The medicine was manufactured by Inventia Healthcare Limited in India. The medicine was distributed through Risiong Pharma Holdings, Inc in East Brunswick, New Jersey. 

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  • Cheese product recall upgraded to FDA’s most serious risk level due to listeria concerns | Cheese…

    Cheese product recall upgraded to FDA’s most serious risk level due to listeria concerns | Cheese…

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    Cheese product recall upgraded to FDA's most serious risk level due to listeria concerns

    The Food and Drug Administration has elevated a nationwide cheese recall to its highest risk level after testing confirmed the presence of a bacteria that can cause severe illness and is potentially deadly.

    The FDA last week upgraded the recall to a Class I, which means “there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.”

    There have been no reports of confirmed illnesses linked to the recall.

    The original recall initiated by the Ambriola Company was issued on Nov. 25, 2025, after routine testing found traces of listeria monocytogenes in cheese products. The specific type of bacteria detected can lead to a listeria infection, which can cause severe illness, especially in pregnant women, older adults, young children and people with weakened immune systems.

    Cheese recalled in 20 states, including Oregon, bumped to highest FDA risk level due to listeria concerns

    Several thousand containers of grated cheese recalled last year due to listeria concerns have been bumped up to the U.S. Food and Drug Administration’s most high-risk recall category.

    In November, the Ambriola Company, a New Jersey-based importer of Italian food products, issued a nationwide recall of more than 11,500 units of grated Pecorino Romano cheese confirmed to be contaminated with listeria.

    The FDA upgraded the incident to Class I recall Tuesday, meaning there is “reasonable probability” that exposure to the product will cause “serious adverse health consequences or death.” Class I is the highest danger level assigned to recalls by the FDA.

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