Twin Cities Co-Op Partners La Reyna Salsa Verde, Gluten Free / Medium recall — FDA F-1497-2023
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
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.
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Listeria monocytogenes
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
A piece of brittle plastic was found in seafood crabmeat stuffing mix.
Listeria monocytogenes
Product appears to be Yellow Oleander instead of Nuez de la India as labeled.
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Listeria monocytogenes
Dips and sauces received out of temperature specifications. Product was not quarantined; product was shipped to customers.
Product may contain metal fragments (ferrous metal, 1 mm or less in size)
Cheese may be contaminated with Listeria monocytogenes.
Inadvertent release of rejected product to market
Potential presence of wood fragments.
Perishable products were not held at an appropriate temperature.
Perishable products were not held at an appropriate temperature.
Undeclared allergen; milk
Perishable products were not held at an appropriate temperature.
Undeclared allergen; milk
Perishable products were not held at an appropriate temperature.
Perishable products were not held at an appropriate temperature.
Signs of bloating in juice cups
Perishable products were not held at an appropriate temperature.
Undeclared allergen; milk
Perishable products were not held at an appropriate temperature.
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.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
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.