📚 Extracted Documents

This is a voluntary recall advisory issued by Cargill Animal Nutrition & Health regarding Nutrena® Country Feeds® Cracked Corn for livestock, due to elevated levels of aflatoxin that exceed FDA action levels. The advisory provides details about the affected product, potential health risks to livestock, and instructions for consumers to stop using the product and return it for a refund. The document emphasizes that no reports of illness have been received and that the recall is conducted with the knowledge of the FDA.

This is an FDA announcement by Bakkavor USA regarding a recall of 16-ounce Meal Simple Red Lentil Dal Soup due to undeclared milk allergens. The recall affects products distributed from November 3, 2025, to December 8, 2025, sold in H-E-B stores in Texas. Consumers are advised to return the product to the place of purchase for a full refund; no illnesses have been reported.

This document details a nationwide recall issued by MediNatura New Mexico, Inc. for their ReBoost Nasal Spray due to microbial contamination, specifically with yeast/mold and Achromobacter. This recall is conducted with the FDA's knowledge, and consumers are advised to stop using the product immediately and return it if purchased. The recall highlights potential adverse health effects, particularly for immuno-compromised individuals.

This document is an advisory from Lunds & Byerlys announcing a voluntary recall of L&B Monster Cookies due to incorrect product labeling that omitted the presence of peanuts, egg, and soy allergens. The announcement includes recall details, a refund offer, and contact information for customer inquiries. The recall spans products available between November 15, 2025, and December 9, 2025, and is published by the FDA on December 10, 2025.

This document is an advisory issued by the FDA detailing a voluntary recall by Lil’ Turtles of its Grandma Belle’s Tomato Basil Soup due to the presence of an undeclared milk allergen on the label. The recall was initiated following a routine inspection by the Ohio Department of Agriculture, and customers with allergies are advised to avoid consumption. Contact information for concerns is provided, and no illnesses have been reported thus far.

This document is an FDA advisory announcing the recall of Lucky Foods brand Cinnamon Powder by TBC Distribution Corporate due to potential contamination with elevated levels of lead. It provides details about the product, distribution locations, and health risks associated with lead exposure. The advisory urges consumers to avoid consumption and offers company contact information for further inquiries.

This document is a safety alert issued by Mellace Family Brands California, Inc. regarding a recall of Wegmans Deluxe Mixed Nuts due to potential Salmonella contamination. The recall affects specific lot codes of 34 oz and 11.5 oz packages sold in various states within the US. Consumers are advised to return the products for a refund and contact Wegmans for any questions.

This document is an advisory from the FDA regarding a recall by Fromm Family Foods of its Bonnihill BeefiBowls Beef Recipe dog food due to potential plastic contamination. Consumers are advised to stop feeding the product to their pets and return it to retailers, as ingestion could lead to health issues in dogs. The advisory was voluntarily initiated by the company with the knowledge of the FDA.

This document is an advisory from the FDA concerning a voluntary recall by Mondelēz Global LLC of RITZ Peanut Butter Cracker Sandwiches due to potential undeclared peanut allergens. The recall, limited to specific products distributed in eight U.S. states, is a precautionary measure to prevent allergic reactions in consumers with peanut allergies. The recall is being conducted in coordination with the U.S. FDA.

Vetoquinol USA, Inc. is recalling six lots of FOLLTROPIN Injectable Kits for cattle due to the detection of particulate matter in the sterile diluent vials, which could cause adverse reactions in animals. The FDA is aware of this recall, and consumers are advised to stop using the affected products immediately and quarantine them. Consumers are instructed to contact Vetoquinol for further instructions, and can report adverse events to the FDA.