HEMU TRADING Black label with blue lettering recall — FDA H-0686-2026
product tested positive for 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.
15,282 detailed records are currently available in this category.
product tested positive for Listeria Monocytogenes.
Product(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40
Undeclared hazelnut and soy lecithin.
Product(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40
Undeclared milk.
Product may be contaminated with Salmonella.
Undeclared milk.
Undeclared milk.
Hard corn starch lumps were found in the product
Ingredients statement declares Anchovy and Sasame, but Contains statement does not declare Fish (Anchovy) and Sesame.
High sugar content. The firm was notified by the FDA that sample results were positive for a high C4 sugar content.
mislabeled Coconut Date Bites. (product is coconut covered, label is for regular date bites)
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Label declares cream cheese but does not declare milk
FDA analysis revealed the presence of undeclared sildenafil
Products contain banned sweetener: cyclamates.
FDA analysis revealed the presence of undeclared sildenafil
Products contain banned sweetener: cyclamates.
Potential Salmonella Contamination
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
FDA analysis revealed the presence of undeclared sildenafil and Tadalafil
Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.
Contains undeclared egg, soy, and hazelnut
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.