Bader Enterprises Premium Food Bubble Gum, packed in 2.5 oz clear flexible recall — FDA H-0539-2026
Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
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.
15,282 detailed records are currently available in this category.
Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
Water was bottled under insanitary conditions.
Product contains undeclared cyclamates.
Product contains undeclared cyclamates.
Potential contamination with Salmonella.
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Water was bottled under insanitary conditions.
Ingredients List declares peanut but the Contains statement does not declare peanut
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Listeria monocytogenes
Water was bottled under insanitary conditions.
Uneviscerated Fish
Potential contamination with leachable lead.
Potential to be contaminated with Salmonella
Label declares bovine colostrum but does not declare milk allergen.
Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad.
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Potential contamination with leachable lead.
foreign material (small hard plastic fragments)
Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
Undeclared allergen - milk. Product contains butter; cream is listed as a sub-ingredient of the butter, but milk is not declared in the ingredients or a contains statement.
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
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.