Fruiti Pops 4 oz recall — FDA F-1736-2012
The firm initiated the recall because the product may contain egg yolk.
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.
19,449 detailed records are currently available in this category.
The firm initiated the recall because the product may contain egg yolk.
The products contain synthetic equivalents of spermine and/or spermidine, which are constituents or extracts of an herb or other botanical, and the that a synthetic copy of a constituent or…
Soybean sprouts may be contaminated with Listeria monocytogenes.
The products contain synthetic equivalents of spermine and/or spermidine, which are constituents or extracts of an herb or other botanical, and the that a synthetic copy of a constituent or…
The firm recalled 26 products for undeclared allergens. This product was recalled due to undeclared yellow #6 and yellow #5.
Cedar's Bakery White Pita Bread, does not list the source of the flour ingredient as wheat, an allergen.
product has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
The firm recalled 26 products for undeclared allergens. This product was recalled due to undeclared soy (soy bean oil and soy flour).
As of May 1, Korean shellfish imports have been blocked by the United States because Korean waters may have been polluted. FDA said that all Korean certified shippers of molluscan shellfish…
Korean oysters have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Ultradent is recalling 36 lots of cinnamon flavored Xylishield gum sold in cartons containing 60 individual pieces as well as within the Xylishield dental care kit due to the omission of…
The firm recalled 26 products for undeclared allergens. This product was recalled due to undeclared milk (nonfat milk), Soy (soybean oil and soy flour), FD&C yellow #6, and wheat (flour).
Ultradent is recalling 36 lots of cinnamon flavored Xylishield gum sold in cartons containing 60 individual pieces as well as within the Xylishield dental care kit due to the omission of…
The firm recalled 26 products for undeclared allergens. This product was recalled due to undeclared YELLOW #6.
The product contains in excess of 23 ppb inorganic arsenic which exceeds the FDA published level of concern for a chronic exposure.
The products were manufactured using a roast meat flavor yeast extract recalled by DSM Nutritional Products, Llc. because it is contaminated with Salmonella.
product containing mussel has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious…
The products were manufactured using a roast meat flavor yeast extract recalled by DSM Nutritional Products, Llc. because it is contaminated with Salmonella.
The firm recalled 26 products for undeclared allergens. This product was recalled due to undeclared yellow #6.
Ultradent is recalling 36 lots of cinnamon flavored Xylishield gum sold in cartons containing 60 individual pieces as well as within the Xylishield dental care kit due to the omission of…
Wheat germ product is contaminated with metal fragments, approximately 0.5mm in diameter and range 3-15mm in length.
As of May 1, Korean shellfish imports have been blocked by the United States because Korean waters may have been polluted. FDA said that all Korean certified shippers of molluscan shellfish…
The firm recalled 26 products for undeclared allergens. This product was recalled due to undeclared yellow #6.
The product has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
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.