Pdx Aromatics WHITE VEIN Kratom CAPSULES, sold under brand names Kraken recall — FDA F-1525-2018
Kraken Kratom, Phytoextractum, and Soul Speciosa WHITE VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.
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.
17,346 detailed records are currently available in this category.
Kraken Kratom, Phytoextractum, and Soul Speciosa WHITE VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.
Possible Pest Contamination at production facility.
Firm recalled product after finding high levels of coliforms, as well as Serratia liquefaciens.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Customer notified firm after they received a positive result for Salmonella of Lot #90186-00 Cardamon Pods Green Whole Organic supplied by Starwest Botanicals
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
The firm is recalling the products listed below because it is mislabeled. Products labeled as Vegan Buffalo Chicken Bites are in fact Vegan Sonoma Chicken Salad. The label fails to declare…
9 inch Asparagus and Goat Cheese Quiche is recalled because egg is declared in the Ingredients statement but it is not declared in the Contains statement.
The frozen waffle product contains whey but fails to declare the major food allergen "milk" on the label
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Maple Minis are recalled due to undeclared soy lecithin.
Firm is recalling Nut-Free Basil Pesto due to mislabeling, causing undeclared tree nuts.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Almond Love Bars are recalled due to undeclared soy lecithin.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Sharp edges were observed on several of the cans which have the potential of causing cuts on the mouths of consumers who use the product.
Sharp edges were observed on several of the cans which have the potential of causing cuts on the mouths of consumers who use the product.
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
Sharp edges were observed on several of the cans which have the potential of causing cuts on the mouths of consumers who use the product.
Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
The firm was notified by a customer that the product label did not list the allergens Yellow #5 & Red 40.
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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