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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19676–19700 of 90011

  • HighFDA (Food)·F-0844-2023·2023-05-17

    Caramel Rum Truffle Recalled for Undeclared Soy, Milk, and Tree Nut Allergens

    Windy Hill Chocolate LLC is recalling Caramel Rum Truffle candies (Batch #1023220097) for undeclared soy, milk, and tree nut allergens. Affected consumers should not consume the product if they have allergies to these ingredients.

    Product
    Caramel Rum Truffle
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0822-2023·2023-05-17

    Dr. Rico Perez Super Kids Colostrum Dietary Supplement Recalled for Undeclared Milk Allergen

    Dr. Rico Perez Super Kids Colostrum chewable tablets are being recalled because the product contains milk but does not declare this allergen on the label. Consumers with milk allergies may be at risk.

    Product
    Dr. Rico Perez Super Kids Colostrum, 60 count chewable tablets dietary supplement, Supplement Facts: 200 mg Colostrum per 1 tablet. HDPE bottle. UPC 8 79840 00044 6. Mfg For: Rico Perez Prod., In2295 Coral Way, Miami, FL 33145.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0883-2023·2023-05-17

    Smoked Swordfish Dip Recalled for Undeclared Yellow #5 Color Additive

    Borris Brothers voluntarily recalls 55 containers of Smoked Swordfish Dip (8oz) distributed in Florida due to undeclared Yellow #5, a color additive that can trigger reactions in sensitive individuals.

    Product
    Smoked Swordfish Dip, Net Wt. 8oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0865-2023·2023-05-17

    Mangetsu Ebisen Crackers Recalled for Undeclared Krill Allergen

    Mangetsu Ebisen 54g crackers are recalled because krill is present in the product but not listed in the ingredients statement, only in a general shellfish warning.

    Product
    Mangetsu Ebisen 54g UPC: 4901053011370
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0846-2023·2023-05-17

    Coffee Bonbon with Undeclared Soy, Milk, and Tree Nut Allergens Recalled

    Windy Hill Chocolate LLC is recalling Coffee Bonbon products due to undeclared allergens including soy, milk, and tree nuts. These allergens are not declared on the product label, posing a risk to consumers with allergies.

    Product
    Coffee Bonbon
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1571-2023·2023-05-17

    PDS Plus Antibacterial Suture Potential Breakage During Intraoperative Use

    Ethicon recalled 1,656 units of PDS Plus Antibacterial Suture due to potential breakage during surgery, which could compromise tissue approximation. The affected lot was distributed to the United Kingdom, Ireland, and Turkey.

    Product
    PDS¿ Plus Antibacterial (polydioxanone) Suture - PDS PLUS CLR 27IN(70CM) USP3-0(M2) S/A PC-25 PRIME. Intended for use in general soft tissue approximation, including use in pediatric cardiovascular tissue. Product Code: PDP9625H
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0879-2023·2023-05-17

    Kurata Foods Vegetable Potage V Ramen recalled for unlisted coconut allergen

    DAISO CALIFORNIA WAREHOUSE is recalling Kurata Foods Vegetable Potage V Ramen because coconut was not listed in the ingredients or allergen statement. The product was distributed across multiple U.S. states and British Columbia Canada.

    Product
    Kurata Foods Vegetable Potage V Ramen 2 servings UPC: 4906436005304
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1573-2023·2023-05-17

    Laboratory Management Software May Display Incorrect Slide Labels

    TDHisto/Cyto laboratory management software may display incorrect information on slide labels in specific use cases. The FDA has issued a Class II recall affecting laboratories nationwide in California.

    Product
    TDHisto/Cyto - A software product used for managing medical information in the field of laboratories performing histology, nongynecological and gynecological cytology and autopsy activities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0843-2023·2023-05-17

    Bourbon Truffle recalled for undeclared soy, milk, tree nut allergens

    Windy Hill Chocolate LLC is recalling Bourbon Truffle candies due to undeclared allergens: soy, milk, and tree nuts. Consumers with allergies to these ingredients should not consume the product.

    Product
    Bourbon Truffle
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1570-2023·2023-05-17

    M-Close Kit suturing apparatus recalled due to plastic housing fracture risk

    New Wave Endo-Surgical is recalling the M-Close Kit surgical suturing apparatus because the plastic housing may fracture. The recall affects 295 units distributed in Florida, Massachusetts, and Georgia.

    Product
    M-Close Kit, REF 27-101; a disposable, ligature passing, suturing apparatus and needle guide for the abdominal wall
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0850-2023·2023-05-17

    Key Lime Bonbon Recalled for Undeclared Soy, Milk, Tree Nuts

    Windy Hill Chocolate LLC recalls Key Lime Bonbons due to undeclared allergens (soy, milk, tree nuts). Consumers with allergies should not consume this product.

    Product
    Key Lime Bonbon
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0859-2023·2023-05-17

    Sunrise Mimosa chocolate recalled for undeclared soy, milk, and tree nuts

    Windy Hill Chocolate LLC is recalling Sunrise Mimosa chocolate due to undeclared allergens: soy, milk, and tree nuts. Consumers with allergies or sensitivities to these ingredients should not consume this product.

    Product
    Sunrise Mimosa
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·23V346000·2023-05-16

    Dennis Eagle Recalls 2020-2023 ProView Vehicles for Short Seat Belts

    Dennis Eagle is recalling 2020-2023 ProView vehicles because the driver's seat belt is too short and difficult to buckle, increasing injury risk.

    Product
    DENNIS EAGLE — DENNIS EAGLE PROVIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V348000·2023-05-16

    Western Star 57X Recalled for Turn Signal Software Defect

    Daimler Trucks North America is recalling 2023 Western Star 57X vehicles because interior turn signals may flash too quickly, potentially masking burnt-out exterior bulbs and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR 57X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V347000·2023-05-16

    2020-2022 Porsche Taycan Brake Warning Indicator Defect Recall

    Porsche is recalling 2020-2022 Taycan vehicles because the brake pad wear warning indicator displays an incorrect color, potentially causing drivers to misinterpret the warning and drive on worn brake pads with reduced braking performance.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V344000·2023-05-12

    2023 Ford F-250, F-350, F-450 Super Duty Steering Column May Separate

    Ford is recalling certain 2023 F-250, F-350, and F-450 Super Duty vehicles due to loose or missing steering column bolts that could cause steering column separation, increasing the risk of crashes due to loss of steering control.

    Product
    FORD — FORD F-350 SD, F-250 SD, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V341000·2023-05-12

    Forest River Recalls 2022-2023 Rockport Work Trucks for Brake Wiring

    Forest River is recalling 2022-2023 Rockport work trucks because the trailer brake controller may be incorrectly wired, which can cause a loss of brake function and increase crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V343000·2023-05-12

    Fox Factory Recalls Winch Remotes on 2021-2023 Jeep, GM, Ford, RAM Vehicles

    Fox Factory is recalling 1,578 vehicles equipped with Warn winches because water may enter the remote, corrode the circuit board, and cause the winch to operate unintentionally.

    Product
    FOX FACTORY — FOX FACTORY FORD PICKUP, GM PICKUP, RAM PICKUP, JEEP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V342000·2023-05-12

    2020-2023 Ford Explorer and Lincoln Vehicles Rearview Camera Failure

    The rearview camera video output may fail on certain 2020-2023 Ford Explorer and Lincoln vehicles, reducing rear visibility and increasing crash risk. Ford will replace the camera free of charge.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR, AVIATOR, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23201·2023-05-11

    Peloton Exercise Bikes Recalled for Seat Post Breakage and Fall Risk

    Peloton is recalling approximately 2.2 million Model PL01 exercise bikes because the seat post assembly can break during use, causing users to fall. The company has received 35 reports of seat post breakage, including 13 reports of injuries such as fractured wrists, lacerations, and bruises.

    Product
    Peloton Bikes Model PL01
    Category
    Consumer Product
    Distribution
    Distributed nationwide