BAPS SHAYONA Kaju Pista Roll Sweet rolls made from cashew and recall — FDA F-0490-2024
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6 and Blue 1.
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.
15,640 detailed records are currently available in this category.
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6 and Blue 1.
During an FDA inspection the firm was notified that some of their products contains undeclared soy.
During an FDA inspection the firm was notified that some of their products contains undeclared soy and Yellow #5 & #6.
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6.
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5, Green 3.
Undeclared milk and soy
Undeclared allergen; milk
Undeclared milk and soy
Undeclared milk and soy
Undeclared milk and soy
Undeclared milk and soy
Potential E. coli (EHEC) contamination
undeclared soy lecithin.
FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.
potentially contaminated with peanut
Sub-ingredients not declared for sunflower butter.
Undeclared allergens: Milk, soy, and wheat.
Undeclared allergen: Milk. Undeclared Color Additives: FD&C red #5, blue #1, red #3, red #40, yellow #5.
Undeclared allergens: Milk and Tree Nuts. Undeclared color additives: FD&C yellow #5, yellow #8, red #40.
Undeclared allergen: Milk, tree nuts, peanuts, soy, and wheat.
Undeclared allergen: Milk. Undeclared color additives: FD&C red #6, red #5, yellow#5.
Sub-ingredients not declared for sunflower butter.
Undeclared allergen: Milk.
Undeclared allergen: Milk, soy, and wheat.
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.