Wiers Farm - Spaghetti Squash packaged in 1lb cartons - case recall — FDA F-1701-2024
Listeria monocyotgenes contamination
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.
Listeria monocyotgenes contamination
Listeria monocyotgenes contamination
Undeclared gluten
Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
Possible contamination with Listeria monocytogenes
Possible contamination with Listeria monocytogenes
Mustard potato salad is being recalled due to plastic foreign material.
Toxic levels of muscimol
Undeclared Allergen - Wheat
Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
Elevated levels of cadmium in plates
Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).
Potential undeclared gluten product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.
Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).
Undeclared peanuts
Product was recalled due to the temperature being over 40 degrees and not on ice July 1st, 2024
Potential undeclared gluten product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.
Allergen (sesame seeds) declared in the ingredient statement but missing from the "Contains" statement
Potential under-processing.
Product may be contaminated with Listeria monocytogenes.
Potential under-processing.
Product contains elevated levels of undeclared sulfites.
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.