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.
16,964 detailed records are currently available in this category.
Biscotti- Plain product is recalled because the ingredients statement on the master bulk case label declared butter but it does not declare milk.
Granola products may contain pieces of foreign material.
Customer discovered that some bags of dark chocolate non pareils contain dark chocolate almonds.
Complaints received of irregular pieces of soft plastic in the product.
Firm has received complaints of finding pieces of glass in the products.
Granola products may contain pieces of foreign material.
New York State Department of Agriculture and Markets sampled and tested Rattan Roots in Brine and found high levels of sulfites which are not declared on the label.
Granola products may contain pieces of foreign material.
Product label lists butter as an ingredient but does not declare milk.
Product label lists butter as an ingredient but does not declare milk.
NYSDAM found Listeria Monocytogenes in Cheese during sampling.
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Raw California Orange Blossom Honey was recalled due to two random FDA samples tested for unapproved fumagillin (antibiotic drug) residue.
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Dried spice and herb products potentially contaminated with generic E. coli.
Mislabeling and Undeclared allergens: Baked Potatoes with Cheddar Cheese & Bacon were mislabeled as Herb Roasted Potatoes.
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
FDA Issued Shutdown Letter ordering the recall of all produced juices in violation of Consent Decree of Injunction
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
FDA import sample found Salmonella poly D in White Headless Shrimp- lot not released. Firm is recalling two additional lots as they are from the same packer and were received in the same…
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.
