Washington Crab Recalls Blue Crab Dip 8 oz, Cocktail Sauce 8 oz, Cole Slaw 8 oz and 16 oz & Crabcake 2, 6 & 12 Count Packages Due to Undeclared Milk, Egg, Wheat, Fish & Soy Allergens

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Washington Crab & Seafood Company is recalling their Blue Crab Dip, 8 oz container, Cocktail Sauce 8 oz container, Cole Slaw 8 oz & 16 oz containers & Crabcake 2 count, 6 count & 12 count packages due to undeclared Milk, Egg, Wheat, Fish & Soy allergens. People who have an allergy or severe sensiti

Source: Food and Drugs Administration--Recalls/Safety Alerts

Rico Perez Products, Inc. Issues Allergy Alert on Undeclared Milk in Super Kids Colostrum

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Rico Perez Products, Inc. of Miami, Florida is voluntarily recalling 60-count bottles of Dr. Rico Perez Super Kids Colostrum chewable tablets, because they may contain undeclared milk allergen. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening aller

Source: Food and Drugs Administration--Recalls/Safety Alerts

Wismettac Asian Foods Issues Allergy Alert on Undeclared Fish (Skipjack Tuna) in Udon Noodle

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Wismettac Asian Foods, Inc., Santa Fe Springs, CA is recalling 19.04 oz packages of Shirakiku brand Ajhei Sanuki Udon Noodle. The product contains the undeclared allergen of fish, specifically skipjack tuna. People who have an allergy or severe sensitivity to skipjack tuna run the risk of serious or

Source: FDA Food Safety Recalls RSS Feed

Wellness Natural USA Inc. Expands Allergy Alert on Undeclared Cashews in SimplyProtein® Peanut Butter Chocolate Crispy Bars

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Wellness Natural USA Inc. of Wilmington, DE is expanding their voluntary recall of its SimplyProtein® Peanut Butter Chocolate Crispy Bar, which is sold in a 15-count variety pack that contains two other flavors, because it may contain undeclared cashews. The initial recall which included a single lo

Source: Food and Drugs Administration--Recalls/Safety Alerts

Fresh Express Incorporated Announces Precautionary Recall of Expired Fresh Salad Kits Due to Potential Health Risk

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Fresh Express Incorporated is voluntarily recalling a limited quantity of three varieties of already-expired branded and private label salad kit products produced at the company’s Morrow, Georgia facility

Source: Food and Drugs Administration--Recalls/Safety Alerts

Meijer Recalls Select Premade Salads Due to Potential Health Risk

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Meijer, in conjunction with its supplier, Revolution Farms, is announcing a voluntary recall of select Fresh From Meijer premade salads because they have the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal in

Source: FDA Food Safety Recalls RSS Feed

Revolution Farms, LLC Announces Expanded Recall of Lettuce Due to Possible Health Risk

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Revolution Farms, LLC of Caledonia, Michigan is expanding the voluntary recall announced on April 5, 2023 to include all products sold under the Revolution Farms brand. All date codes are included in this recall. The recalled product has the potential to be contaminated with Listeria monocytogenes,

Source: Food and Drugs Administration--Recalls/Safety Alerts

Karma Spices and Trading Company, LLC Issues Allergy Alert on Undeclared Milk in White Cheddar Cheese Popped Water Lily Seeds

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Karma Spices and Trading Company, LLC of Walled Lake, Michigan is recalling White Cheddar Cheese Popped Water Lily Seeds, because it may contain undeclared Milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume the

Source: FDA Food Safety Recalls RSS Feed

Revolution Farms Announces the Voluntary Recall of Lettuce Because of Possible Health Risk

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Revolution Farms of Caledonia, Michigan is voluntarily recalling the listed products packed between 3/3/23 and 3/11/23, because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elder

Source: Food and Drugs Administration--Recalls/Safety Alerts

Abbott Issues Safety Notification for FreeStyle Libre® Family of Readers in the U.S.

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Abbott initiated a voluntary medical device correction in February to emphasize instructions for its FreeStyle Libre®, FreeStyle Libre® 14 day and FreeStyle Libre® 2 Readers in the United States due to a limited number of reports worldwide (0.0017%) from users over several years that their reader’s

Source: Food and Drugs Administration--Recalls/Safety Alerts