Alimentos Kamuk Internacional (Costa Rica) S. A TROPICAL PEPPER CO recall — FDA F-1842-2018
Sodium values reported on the product label are not consistent with the current value.
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.
17,346 detailed records are currently available in this category.
Sodium values reported on the product label are not consistent with the current value.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice Beverages due to packaging concerns following multiple reports of leaking caps.
HP Hood LLC, has initiated a recall of Blue Diamond Almond Breeze Almond Milk, Half Gallon, because the product tested positive for milk allergen.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice Beverages due to packaging concerns following multiple reports of leaking caps.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice Beverages due to packaging concerns following multiple reports of leaking caps.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice Beverages due to packaging concerns following multiple reports of leaking caps.
Potential blood contamination.
Sodium values reported on the product label are not consistent with the current value.
Product contains high levels of undeclared sulfites.
Roasted Chestnut loose leaf tea contains undeclared slivered almonds.
Pasta Spinach with Cavatappi Reser's Fine Food is recalled due to a potential contamination with Cyclospora. The pasta salad contains spinach that was recalled due to a potential…
Product may be contaminated with Listeria monocytogenes.
Mediterranean Salad Vegan is recalled because milk is declared in the Ingredients statement but it is not declared in the Contains statement.
Saratoga Food Specialties, has initiated a voluntary recall of Pizza Hut Seasonings following their supplier's recall of dry whey powder due to the potential presence of Salmonella
FDA inspection found two lots of supplements that did not declare shellfish as an ingredient on the product label; shellfish is properly declared on website.
Severino Pasta Manufacturing, Inc. has initiated a recall of their Severino Pasta Super Fresh Cheese Raviolini due to undeclared eggs. The retail unit has the correct label on top, Cheese…
Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin, FD&C Yellow #6 (Sunset Yellow FCF), FD&C Red #40…
Some containers of ice cream in a Peanut Butter Cup flavor container have a Butter Pecan flavor lid and are filled with Butter Pecan ice cream.
Grizzlies Brand and Grizzlies Granolas Oregon Trail Mix are recalled due to undeclared milk.
Whole Foods Market, Inc. has initiated a recall of various bakery products that was made in there Mid-Atlantic stores and sold between May 25th and July 13th which failed to declare soy…
Whole Foods Market, Inc. has initiated a recall of various bakery products that was made in there Mid-Atlantic stores and sold between May 25th and July 13th which failed to declare soy…
Matiz Apricot Bar Demi-luna 8.8 ounces bar is recalled because customer found two small plastic pieces in the product.
Pepperidge Farm has been notified by one of its ingredient suppliers that whey powder in a seasoning that is applied to four varieties of Goldfish crackers has been the subject of a recall…
Whole Foods Market, Inc. has initiated a recall of various bakery products that was made in there Mid-Atlantic stores and sold between May 25th and July 13th which failed to declare soy…
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.
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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.