The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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24451–24475 of 114492

  • SevereNHTSA·23V213000·2023-03-29

    Volkswagen Recalls 2023 ID 4 Vehicles for Door Handle Water Ingress

    Volkswagen is recalling 2023 ID 4 vehicles because water can enter the door handle circuit board, causing doors to open unexpectedly at low speeds.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID 4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V215000·2023-03-29

    2018-2021 Volkswagen Atlas Front Passenger Air Bag Sensor Fault

    Volkswagen is recalling certain 2018–2021 Atlas and 2020 Atlas Cross Sport vehicles because a wiring fault in the passenger occupant detection system may deactivate the front passenger air bag when the seat is occupied.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0638-2023·2023-03-29

    ITOSEIKA Chocolate Chip Cookies Recalled for Undeclared Milk Allergen

    ITOSEIKA chocolate chip cookies are being recalled due to undeclared milk allergen on the label. Consumers with milk allergies should not consume this product.

    Product
    ITOSEIKA Chocolate chip cookies 10pieces UPC: 4901050111400 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0631-2023·2023-03-29

    Rice Crackers Recalled Due to Undeclared Wheat Allergen

    DAISO CALIFORNIA WAREHOUSE is recalling IWATSUKASEIKA Ajishirabe Rice Crackers because the label fails to declare wheat. Wheat is a major allergen that can cause severe allergic reactions in sensitive individuals.

    Product
    IWATSUKASEIKA Ajishirabe Rice Crackers UPC: 4901037117746 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0643-2023·2023-03-29

    Pistachio wasabi snack recalled for undeclared soy allergen

    SENNARIDO Green Snack Pistachio-Wasabi Flavor (90g) is recalled because soy is not declared on the label. Approximately 10,986 units were distributed across California, Washington, Nevada, Texas, New York, New Jersey, and Canada.

    Product
    SENNARIDO Green Snack Pistachio -Wasabi Flavor 90g UPC: 4974120431715 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·23V212000·2023-03-29

    Audi Recalls 2020 Q7 Vehicles Due to Front Camera Fire Risk

    Audi is recalling 2020 Q7 vehicles because a software incompatibility may cause the front camera heating element to overheat, increasing the risk of a fire.

    Product
    AUDI — AUDI Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0633-2023·2023-03-29

    Powdered lemon tea recalled for undeclared milk allergen

    MEITO An extra Stick Powdered Lemon Tea is recalled because the product contains milk that is not declared on the label. Consumers with milk allergies who have purchased this product should not consume it.

    Product
    MEITO An extra Stick Powdered Lemon Tea 5packs UPC: 4902757442804 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0630-2023·2023-03-29

    Sesame sauce recalled due to undeclared wheat allergen

    Shinsei Additive Free Sesame Sauce is being recalled because wheat allergen was not declared on the product label. Consumers with wheat allergies who consume this product may experience allergic reaction.

    Product
    Shinsei Additive Free Sesame Sauce 22g UPC: 4901665004616 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·23V218000·2023-03-29

    Kia Recalls 2015-2019 Soul EV Vehicles for Battery Fire Risk

    Kia is recalling 2015-2019 Soul EV vehicles with E400 batteries because an electrical short-circuit could cause a fire. Owners should contact Kia for a free software update or battery replacement.

    Product
    KIA — KIA SOUL EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0640-2023·2023-03-29

    SENNARIDO pistachio snack recalled for undeclared soy allergen

    DAISO CALIFORNIA WAREHOUSE is recalling SENNARIDO Green Snack Pistachio 90g because the product contains undeclared soy, a major food allergen that poses allergic reaction risk to sensitive consumers.

    Product
    SENNARIDO Green Snack Pistachio 90g UPC: 4974120413421 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0488-2023·2023-03-29

    Delsam Pharma Artificial Eye Ointment Recalled for Bacterial Contamination

    Delsam Pharma's Artificial Eye Ointment is being recalled for bacterial contamination in unopened tubes. FDA analysis found non-sterility defects in approximately 50,000 units.

    Product
    Delsam Pharma's Artificial Eye Ointment (Mineral Oil 15%, White Petrolatum 83%), 3.5 grams (1/8 oz.) tube, Distributed By: Delsam Pharma Lic, Bronx, Newyork 10469, NDC 72570 122 35, UPC 3 72570 12235 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0642-2023·2023-03-29

    Kurata Menzo Ramen Recalled for Undeclared Coconut Allergen

    DAISO CALIFORNIA WAREHOUSE is recalling Kurata Menzo Meatfree Tonkotsu Ramen Dry due to undeclared coconut on the label. Consumers with coconut allergies who consume this product may experience allergic reactions.

    Product
    Kurata Menzo Meatfree Tonkotsu Ramen Dry 2P 238.8g UPC: 4906436004932 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0636-2023·2023-03-29

    Soft rice crackers recalled for undeclared coconut allergen

    DAISO CALIFORNIA WAREHOUSE is recalling 150YEN HIZATSUKI Soft rice crackers because the product contains coconut that was not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    150YEN HIZATSUKI Soft rice crackers sea lettuce soy sauce flavor UPC: 4902445210500 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0634-2023·2023-03-29

    Coffee Candy Recalled for Undeclared Coconut Allergen

    Kanro Non sugar coffee candy is recalled because coconut was not declared on the label, posing a risk to consumers with coconut allergies.

    Product
    Kanro Non sugar coffee candy 40g UPC: 4901351013137 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0699-2023·2023-03-29

    Sprouts Farmers Market Saltine Crackers recalled for potential peanut contamination

    Sprouts Farmers Market is recalling Saltine Crackers Sea Salt Tops due to potential peanut contamination. Approximately 1,050 cases were distributed in Arizona, California, and Georgia.

    Product
    Sprouts Farmers Market Saltine Crackers Sea Salt Tops NET WT 16 OZ (1 LB) 454g UPC 646670310164 packaged in slug wrapper in a cardboard carton, 12 packages per case
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1279-2023·2023-03-29

    Cardiosave IABP Pneumatic Interface Module Recalled for Performance Issue

    Datascope Corp. recalls the Cardiosave IABP Pneumatic Interface Module due to a Safety Disk performance issue that may reduce balloon inflation. Ten specific units with identified serial numbers are affected.

    Product
    Cardiosave Intra-Aortic Balloon Pump (IABP) Pneumatic Interface Module (PIM) , Model Number 0997-00-1178
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0648-2023·2023-03-29

    Kirkland Signature Colombian cold brew coffee recalled for metal contamination

    Berner Foods Inc. is recalling Kirkland Signature Colombian Cold Brew Coffee due to metal contamination in 231,071 cases distributed across 13 states. Consumers should stop using affected products.

    Product
    Kirkland Signature Colombian Cold Brew Coffee ready-to-drink, 12 fl oz in aluminum can, 12 cans per case
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-1281-2023·2023-03-29

    Raystation Treatment Planning System Collimator Angle Export Defect

    Raystation radiation therapy planning software may not correctly export collimator angle settings when using the DICOM export function. In exported files, the collimator angle may be replaced with zero regardless of the user's selection.

    Product
    Raystation treatment planning system for radiation therapy, Model Numbers 9.0.0, 9.0.1, 9.1.0, 9.2.0, 10.0.0, 10.0.1, 10.0.2, 10.1.0, 10.1.1, 11.0.0, 11.0.1, 11.0.3, 11.0.4, 12.0.0, 12.1.0, 12.1.1, 12.0.3, 12.1.2, 12.0.4, 12.1.3, 13.0.0, 13.1.0. Software Version Numbers 9A, 9B…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0650-2023·2023-03-29

    DG Health Sugar Free Daily Fiber Recalled for Missing Phenylalanine Warning

    DG Health Sugar Free Daily Fiber is recalled for missing a required phenylalanine warning label. People with phenylketonuria (PKU) require this warning to safely use the product.

    Product
    DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
    Category
    Food
    Distribution
    47 states
  • HighNHTSA·23V211000·2023-03-29

    BMW seats may not restrain occupants properly in crash

    BMW is recalling certain 2019–2021 3-series and X3/X4 models because the seat frame may not have been welded properly to the seat rails, risking occupant injury in a crash.

    Product
    BMW — BMW M340I, X4, 330I, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0639-2023·2023-03-29

    Japanese Potato Yokan Candy Recalled for Undeclared Coconut

    Kinjo Seika Potato Yokan confection is being recalled because coconut, a major allergen, was not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    Kinjo Seika Potato Yokan 130g UPC: 4901324017056 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1272-2023·2023-03-29

    Disposable Patient Circuit with Precision Flow System recalled for excessive condensation

    Vapotherm has recalled 5,869 Low Flow Disposable Patient Circuits for the Precision Flow System due to reports of excessive condensation that may lead to rainout.

    Product
    Low Flow Disposable Patient Circuit for the Precision Flow System, Product Code PF-DPC-LOW
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1277-2023·2023-03-29

    Cardiosave Hybrid Intra-Aortic Balloon Pump Performance Issue Recall

    Datascope Corp. is recalling specific Cardiosave Hybrid intra-aortic balloon pumps due to a Safety Disk performance issue that may reduce balloon inflation and therapeutic benefit.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Numbers Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0473-2023·2023-03-29

    Daytrana Methylphenidate Transdermal Patches Recalled for Defective Delivery System

    Noven Pharmaceuticals recalls Daytrana (methylphenidate) 30 mg transdermal patches nationwide due to defective delivery system components that fail shear specifications. Patients should contact their healthcare provider regarding medication alternatives.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide