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.
Undeclared allergen: Bread products were manufactured using raw material (wheat gluten) that was recalled due to undeclared peanut and/or tree nut residue.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Undeclared allergen: Bread products were manufactured using raw material (wheat gluten) that was recalled due to undeclared peanut and/or tree nut residue.
Golden Chocolate International, Inc. has recalled (3) products due to the use of undeclared FD&C Yellow #5, FD&C Yellow #6, and FD&C Red #40 food colorings.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
This recall has been initiated due to (mis-labeling) of an undeclared milk allergen on the Cheesecake Shave Ice pouch.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked salmon due to potential Listeria Monocytogenes contamination.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked salmon due to potential Listeria Monocytogenes contamination.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Some containers or Eating Right Black Bean Coup may contain Eating Right Spicy Thai Noodle inside.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.
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.
