Kabobs The Hors d'oeuvre Specialist TRUFFLE ARANCINI WITH WILD recall — FDA F-1553-2022
The firm was notified by their rice supplier that the product may contain small pieces of glass.
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.
16,072 detailed records are currently available in this category.
The firm was notified by their rice supplier that the product may contain small pieces of glass.
Detectable levels of Per- and polyfluoroalkyl substances (PFAS).
Undeclared allergens; wheat and soy.
Elevated levels of lead detected as a result of testing conducted by Maryland Department of Health.
Label declares Whey but does not declare Milk.
Products may be contaminated with Listeria monocytogenes.
Potential to be contaminated with Salmonella.
The product may contain trace amounts of coconut, which is not declared on the labeling. Laboratory analysis was unable to detect any coconut allergen, however the firm has decided to…
Label declares Whey but does not declare Milk.
Acidified/Low Acid dietary supplement with no approved process.
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Potential to be contaminated with Salmonella
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Acidified/Low Acid dietary supplement with no approved process.
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Acidified/Low Acid dietary supplement with no approved process.
Acidified/Low Acid dietary supplement with no approved process.
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Acidified/Low Acid dietary supplement with no approved process.
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
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.