RANDALL ULITMATE 4-BEAN MIX 48OZ glass jars UPC 070095000902 recall — FDA F-0805-2021
Lack of functioning Temperature Indicating Devices in retorts
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.
16,552 detailed records are currently available in this category.
Lack of functioning Temperature Indicating Devices in retorts
Lack of functioning Temperature Indicating Devices in retorts
Positive rainwater test for Listeria monocytogenes. The rainwater came in contact with product.
Lack of functioning Temperature Indicating Devices in retorts
Firm discovered that some containers exhibited post-process spoilage during additional inspection and deployment of product at Distribution Center.
Lack of functioning Temperature Indicating Devices in retorts
Specific lot of Organic Steel Cut Oats, may actually contain Organic Beet Sugar
The firm is recalling Circle K brand Chicken Salad Sandwiches "best buy" date of 6/7/21 through 7/9/21 because the chicken used is subject to a national recall issued by Tyson Foods due to…
FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)
Ingredient tested positive for milk allergen.
Ingredient tested positive for milk allergen.
FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)
FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)
FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (undeclared milk)
Soy Lecithin listed in ingredients statement but soy is not mentioned in the contains statement.
Label declares lecithin but does not declare soy lecithin.
Label declares lecithin but does not declare soy lecithin.
Label declares lecithin but does not declare soy lecithin.
Label declares lecithin but does not declare soy lecithin.
Label declares lecithin but does not declare soy lecithin.
Potential undeclared peanut allergen.
Label declares lecithin but does not declare soy lecithin.
Firm testing found trace levels of yeast in the product. Further investigation found the presence of Candida pelliculosa.
Product may contain elevated levels of inorganic arsenic (above 100ppb)
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.