Haleon has recalled four lots of Gas-X Extra Strength Softgels after a possible coolant contamination issue during packaging. The Gas-X Extra Strength recall affects 125 mg softgels in 120-count and 72-count bottles distributed to the consumer level beginning Monday, April 13, 2026, according to a company announcement published by the U.S. Food and Drug Administration on Thursday, June 4, 2026. Gas-X Extra Strength Recall Covers Four Lots The r
Haleon has recalled four lots of Gas-X Extra Strength Softgels after a possible coolant contamination issue during packaging. The Gas-X Extra Strength recall affects 125 mg softgels in 120-count and 72-count bottles distributed to the consumer level beginning Monday, April 13, 2026, according to a company announcement published by the U.S. Food and Drug Administration on Thursday, June 4, 2026. Gas-X Extra Strength Recall Covers Four Lots The r
Keurig has issued a voluntary recall of more than 80,000 decaf coffee pods after discovering that the products may contain caffeine. The recall applies specifically to K-Cup pods labeled as McCafe Premium Roast Decaf Coffee, with a best-by date of November 17, 2026, and a UPC code of 043000073438. Consumers who purchased these pods are advised to check their inventory, as the product may not meet its labeled decaf specifications. The recall was initially announced on December 6, 2025,
Keurig has issued a voluntary recall of more than 80,000 decaf coffee pods after discovering that the products may contain caffeine. The recall applies specifically to K-Cup pods labeled as McCafe Premium Roast Decaf Coffee, with a best-by date of November 17, 2026, and a UPC code of 043000073438. Consumers who purchased these pods are advised to check their inventory, as the product may not meet its labeled decaf specifications. The recall was initially announced on December 6, 2025,
Federal regulators have announced a sweeping recall affecting hundreds of commonly purchased consumer products sold in small grocery stores and markets across parts of the Midwest, citing serious sanitation concerns that may pose a risk to public health. The action follows an inspection of a Minneapolis-based distribution facility that supplies food, medication, and household goods to retailers in Minnesota, Indiana, and neighboring states. According to the Food and Drug Administrat
Federal regulators have announced a sweeping recall affecting hundreds of commonly purchased consumer products sold in small grocery stores and markets across parts of the Midwest, citing serious sanitation concerns that may pose a risk to public health. The action follows an inspection of a Minneapolis-based distribution facility that supplies food, medication, and household goods to retailers in Minnesota, Indiana, and neighboring states. According to the Food and Drug Administrat
Thousands of cases of popular salad dressings distributed across the United States have been recalled after federal regulators identified the presence of foreign material in certain products, according to a recent enforcement report issued by the Food and Drug Administration. The recall involves products manufactured by California-based Ventura Foods and includes several well-known brands and private-label dressings sold through retail and food service channels. The recall was first
Thousands of cases of popular salad dressings distributed across the United States have been recalled after federal regulators identified the presence of foreign material in certain products, according to a recent enforcement report issued by the Food and Drug Administration. The recall involves products manufactured by California-based Ventura Foods and includes several well-known brands and private-label dressings sold through retail and food service channels. The recall was first
The U.S. Food and Drug Administration has released an updated notice regarding a nationwide recall of shredded cheese products distributed to several major retail chains, including Aldi, Target, and Walmart. According to the agency, more than 260,000 cases of shredded cheese may contain metal fragments, prompting officials to elevate their advisory and urge consumers to take immediate precautions. The update follows recent concerns in the dairy sector, including a separate recall involving Pr
The U.S. Food and Drug Administration has released an updated notice regarding a nationwide recall of shredded cheese products distributed to several major retail chains, including Aldi, Target, and Walmart. According to the agency, more than 260,000 cases of shredded cheese may contain metal fragments, prompting officials to elevate their advisory and urge consumers to take immediate precautions. The update follows recent concerns in the dairy sector, including a separate recall involving Pr
WASHINGTON — The U.S. Food and Drug Administration (FDA) has announced a recall of certain lots of ByHeart Whole Nutrition Infant Formula following a multi-state investigation into a cluster of infant botulism cases. The outbreak, which spans ten states, has resulted in 13 hospitalizations since August, though no deaths have been reported. Federal health officials said the recall applies to two specific lots of ByHeart powdered formula with “use by” dates of December 1. The af
WASHINGTON — The U.S. Food and Drug Administration (FDA) has announced a recall of certain lots of ByHeart Whole Nutrition Infant Formula following a multi-state investigation into a cluster of infant botulism cases. The outbreak, which spans ten states, has resulted in 13 hospitalizations since August, though no deaths have been reported. Federal health officials said the recall applies to two specific lots of ByHeart powdered formula with “use by” dates of December 1. The af
Several over-the-counter eye products have been voluntarily recalled following a U.S. Food and Drug Administration audit that uncovered issues related to manufacturing practices. The recall, issued by AvKARE, involves Artificial Tears Ophthalmic Solution, a commonly used product for treating dry or irritated eyes. According to the recall announcement posted by the company, the products were pulled due to deviations in manufacturing that may have compromised quality and potentially pose a risk
Several over-the-counter eye products have been voluntarily recalled following a U.S. Food and Drug Administration audit that uncovered issues related to manufacturing practices. The recall, issued by AvKARE, involves Artificial Tears Ophthalmic Solution, a commonly used product for treating dry or irritated eyes. According to the recall announcement posted by the company, the products were pulled due to deviations in manufacturing that may have compromised quality and potentially pose a risk