Waiakea Hawaiian Volcanic Water Naturally Alkaline recall — FDA F-1117-2024
Consumer complaints involving floating particles.
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.
15,640 detailed records are currently available in this category.
Consumer complaints involving floating particles.
Product contains Acid Red 18
Undeclared allergen (almond) in Dark Chocolate Cherry Granola
Potential contamination with Clostridium botulinum
Product contains Acid Red 18
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Foreign object; piece of glass.
Bottle of juice was found at the store level with the incorrect sku label.
Product was determined to be under processed.
Elevated levels of vitamin D3
Potential contamination with Salmonella.
Label error during reprint. Says 1000 mg instead of 1000 mcg on the center front panel of the label.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Undeclared wheat. Finished bakery product labels declared flour but did not specify wheat.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Product has the potential to be contaminated with Listeria monocytogenes.
Undeclared wheat. Finished bakery product labels declared flour but did not specify wheat.
Product has the potential to be contaminated with Listeria monocytogenes.
Product contains undeclared wheat.
Due to elevated levels of lead.
Elevated levels of lead found in product
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
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.