Westbrook's Cannery Net WT recall — FDA F-3084-2015
Products potentially underprocessed.
Track recent U.S. food recall enforcement reports from the FDA. Review recalled products, reasons, classifications, recalling firms, distribution details and official record identifiers when available.
18,610 detailed records are currently available in this category.
Products potentially underprocessed.
Products potentially underprocessed.
IEH sample of macadamia nuts was found positive for Salmonella
A small number of think Thin Madagascar Vanilla with Almonds & Pecans oatmeal have the correct lid but have the incorrect Honey Peanut Butter label around the cup. The nuts are obvious once…
Good Seed Inc. of Springfield, VA is voluntarily recalling all packages of soybean sprouts and mung bean sprouts because they have the potential to be contaminated with Listeria…
Products potentially underprocessed.
Kilwins Quality Confections, Inc., is recalling 5 ounce containers of SUGAR FREE Milk Chocolate Caramels because they were incorrectly labeled and may contain undeclared cashew. People who…
Good Seed Inc. of Springfield, VA is voluntarily recalling all packages of soybean sprouts and mung bean sprouts because they have the potential to be contaminated with Listeria…
The powdered golden seal had a coliform count of 2000 cfu/g when the specifications stated less than 1000/cfy/g. There is 12mg of golden seal per dose.
The American Bottling Company is recalling 12 oz. cans of A& W Cream Soda because the front panel bears the statement "caffeine free" and the product contains caffeine
Chetak New York L.L.C. of Edison, NJ is recalling 300 jars of 14.1oz Deep Coriander Powder, Lot# LE15152, because they have the potential to be contaminated with Salmonella, an organism…
IEH sample of macadamia nuts was found positive for Salmonella
Products potentially underprocessed.
Big Train Inc is recalling one single lot of Vanilla Chai Tea Latte mix which is mislabeled. The product is labeled with "No Sugar Added" but actual product contains sugar.
The powdered golden seal had a coliform count of 2000 cfu/g when the specifications stated less than 1000/cfy/g. There is 12mg of golden seal per dose.
The powdered golden seal had a coliform count of 2000 cfu/g when the specifications stated less than 1000/cfy/g. There is 12mg of golden seal per dose.
IEH sample of macadamia nuts was found positive for Salmonella
The powdered golden seal had a coliform count of 2000 cfu/g when the specifications stated less than 1000/cfy/g. There is 12mg of golden seal per dose.
The powdered golden seal had a coliform count of 2000 cfu/g when the specifications stated less than 1000/cfy/g. There is 12mg of golden seal per dose.
Undeclared soy lecithin. Dark Chocolate with Cranberry, Roasted Nuts & Sea Salt contains soy lecithin but label does not declare soy.
The powdered golden seal had a coliform count of 2000 cfu/g when the specifications stated less than 1000/cfy/g. There is 12mg of golden seal per dose.
IEH sample of macadamia nuts was found positive for Salmonella
The firm failed to declare the allergen eggs on their labels.
The products were recalled because a container of Kroger Garlic Powder tested positive for Salmonella during routine FDA retail sampling. Out of an abundance of caution, the firm is…
FDA enforcement reports are classified by potential health hazard. Class I is the most serious classification, while Class II and Class III generally indicate lower levels of risk. The classification shown here comes from the official FDA record.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.