Moonlight Packing UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A recall — FDA H-0316-2026
Potential contamination with Listeria monocytogenes.
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.
768 detailed records are currently available in this category.
Potential contamination with Listeria monocytogenes.
Potential contamination with Listeria monocytogenes.
Potential contamination with Listeria monocytogenes.
Undeclared caffeine
Contaminated with Clostridium botulinum
Potential contamination with Listeria monocytogenes.
Undeclared Soy Protein Concentrate
Clostridium botulinum (uneviscerated fish)
Potential to be contaminated with Clostridium botulinum. Products manufactured without an approved process filed.
Potential metal fragments from supplier raw material (downstream recall)
Potential contamination with Listeria monocytogenes.
Potential metal fragments from supplier raw material (downstream recall)
Undeclared Soy
Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen
Undeclared Sulfite. Shrimp may contain 3.4mg Sulfur Dioxide per serving and label does not declare Sulfite.
The 3oz. sealed packet of Caesar Dressing in Costco Chicken Sandwich w/ Caesar Salad may contain plastic material.
foreign objects (black plastic planting material) in granulated onion
Potential metal fragments from supplier raw material (downstream recall)
Undeclared Soy. The firm received positive test results for soy which is not listed on the label. The firm also noticed that the amount of boron in the product is listed as 250mg per…
Undeclared wheat.
Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303
foreign objects (black plastic planting material) in granulated onion
Products do not declare milk in the Contains statement or the ingredient statement.
Potential metal fragments from supplier raw material (downstream recall)
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.