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July is National Ice Cream Month, and July 20 is National Ice Cream Day. Instead of another scoop of those typical 31 flavors ...
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WISH-TV on MSNBreyers recalls ice cream due to mislabeling and allergensBreyers ice cream has been recalled due to mislabeling, Wendy's is partnering with Takis Fuego to offer a spicy chicken sandwich meal, and Lilly is expanding into heart care by acquiring a gene ...
According to an alert from the FDA, the recall was initiated on June 2 because Breyer’s Rocky Road Ice Cream was incorrectly packaged in a Breyer’s Chocolate Truffle Tub, which poses a risk to ...
Breyers, the popular ice cream brand, has voluntarily recalled one of its products due to mislabeling and "undeclared allergens," according to the Food and Drug Administration (FDA).
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Naples Daily News on MSNBreyers voluntarily recalling mislabeled ice cream. What to knowBreyers is recalling Rocky Road ice cream that was placed in a Chocolate Truffle ice cream packaging, posing a danger to those with almond allergies.
Dairy Foods and the American Dairy Products Institute (ADPI) host the Membrane Technology Forum, an event that serves as a ...
The recall affected specific cases of Breyers Chocolate Truffle 1.5-quart cartons that contained Rocky Road ice cream and ...
How do I know if I have the recalled Breyers ice cream? The ice cream being recalled are Breyers Chocolate Truffle 1.5 quart tubs with UPC code 077567457288 and expiration date/Lot code of JUL1026GB3.
Current nationwide recalls include beef jerky, brown eggs, ice cream and shrimp. Affected items were sold at retailers like ...
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Breyers Ice Creams Recalled After Flavor Containing Life-Threatening Allergen Was Packaged as Another FlavorThe FDA declared this a Class II recall, which is defined as "a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences ...
Unilever subsidiary Breyers has issued a nationwide recall of more than 6,600 cases of Rocky Road ice cream. MelissaMN – stock.adobe.com. The FDA classified the incident as a Class II recall ...
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