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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16476–16500 of 39596

  • SevereFDA (Food)·F-0737-2019·2018-12-12

    Ottogi Jin Ramen Mild Recalled for Undeclared Egg Allergen

    Ottogi America Inc. is recalling Ottogi Jin Ramen Mild 5-packs due to an undeclared egg allergen. The product was distributed in five U.S. states and Canada.

    Product
    Ottogi Jin Ramen Mild NET WT. 1lb 5.16oz, 600g (120gx5) 5PK Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0736-2019·2018-12-12

    Ottogi Jin Ramen Spicy Recalled for Undeclared Egg Allergen

    Ottogi America Inc. is recalling Ottogi Jin Ramen Spicy 5-packs due to an undeclared egg allergen. The product was distributed in five U.S. states and Canada.

    Product
    Ottogi Jin Ramen Spicy NET WT. 1lb 5.16oz, 600g (120gx5) 5PK Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·18V880000·2018-12-11

    Blue Bird Recalls 2019 School Buses for Parking Brake Cable Defect

    Blue Bird is recalling 2019 All American and Vision school buses because the parking brake cable may disengage, allowing the bus to move unintentionally.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V881000·2018-12-11

    Blue Bird Recalls 2019 Transit Buses Due to Parking Brake Defect

    Blue Bird is recalling 2019 All American and Vision transit buses because the parking brake cable may disengage, allowing the bus to move unintentionally.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·120-2018·2018-12-10

    CTI Foods Recalls Pork and Poultry Sausage Due to Metal Contamination

    CTI Foods is recalling frozen Jimmy Dean sausage links that may contain metal pieces. No illnesses have been reported, but consumers should discard the product.

    Product
    CTI Foods LLC. — CTI Foods LLC, Recalls Ready-To-Eat Pork and Poultry Sausage Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V877000·2018-12-10

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Roof Adhesive Defect

    Daimler Trucks North America is recalling 2017-2019 Thomas Built Buses Saf-T-Liner C2 school buses because improperly applied roof adhesive may reduce roof header strength during a rollover crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·119-2018·2018-12-09

    3-D Meats Recalls Beef Snack Sticks for Undeclared Milk Allergen

    3-D Meats, LLC is recalling approximately 47 pounds of ready-to-eat beef snack sticks because they are misbranded and may contain undeclared milk, a known allergen.

    Product
    3-D Meats, LLC Recalls Ready-To-Eat Beef Snack Stick Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V870000·2018-12-07

    PACCAR Recalls 2018 Kenworth and Peterbilt Trucks for Seat Belt Defect

    PACCAR is recalling 2018 Kenworth and Peterbilt trucks because seat belt buckles may be glued instead of sewn, risking separation in a crash.

    Product
    KENWORTH — KENWORTH, PETERBILT T880, T680, 579, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·118-2018·2018-12-07

    Amboy Group Recalls Poultry Products for Undeclared Allergens

    Amboy Group, LLC is recalling raw boneless and skinless poultry products because they are misbranded and may contain undeclared milk, egg, and soy.

    Product
    Amboy Group, LLC Recalls Poultry Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V872000·2018-12-07

    Mercedes-Benz Recalls 2018 C 300 and E 400 for Steering Defect

    Mercedes-Benz is recalling two 2018 vehicles because the steering coupling may not be locked, which could reduce steering ability and increase crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, E 400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V875000·2018-12-07

    Micro Bird Recalls CT-Series Buses for Seat Lock Defect

    Micro Bird is recalling 2015-2018 CT-Series buses because foldaway seats may not stay locked during a crash, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD CT-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0678-2019·2018-12-05

    New Forest LLC Recalls Organic Cardamom Due to Salmonella Risk

    New Forest LLC is recalling 2,723 kgs of Organic Cardamom Green Whole from Guatemala due to potential Salmonella contamination. The product was distributed in Wisconsin and Nevada.

    Product
    Organic Cardamom Green Whole. Product of Guatemala. Product is labeled with a paper label son onto each 25-kg poly-lined, poly-weave "double bag". The label reads - Certified Organic Cardamom Pod Mixed Grade, Certified Organic by Mayacert, Product of Guatemala, Net Weight…
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0664-2019·2018-12-05

    Imported Mexican Cheese Recalled Due to Salmonella Contamination

    Alebrije Imports Inc. is recalling Queseria "La Milagrosa" cheese due to Salmonella contamination found by the California Department of Food and Agriculture.

    Product
    Queseria "La Milagrosa" La Delicia al Paladar. 1/2 kg and 1 kg sizes. Packaged in a plastic bag with a yellow label.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0722-2019·2018-12-05

    Chukar Cherries Ultra Dark Chocolate Cocoa Pecans Recalled for Unlabeled Milk

    Chukar Cherry Company is recalling 569 pouches of Ultra Dark Chocolate Cocoa Pecans because the product contains milk, which is not listed on the label.

    Product
    Ultra Dark Chocolate Cocoa Pecans, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261 22507 1. The label is read in parts: "***ULTRA DARK CHOCOLATE COCOA PECANS***Ingredients: Bittersweet Chocolate (Cacao Beans, Pure Cane Sugar, Unsweetened Chocolate…
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-0507-2019·2018-12-05

    NxStage PureFlow B Solution Recalled for Potential Bag Bursting Hazard

    NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-RFP-456, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V864000·2018-12-05

    Volkswagen Recalls 2018 Golf R Vehicles Due to Fuel Hose Defect

    Volkswagen is recalling 2018 Golf R vehicles because a fuel hose connector may detach, causing a leak that increases fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0514-2019·2018-12-05

    Eurotrol HemoTrol Level 2 Recalled Due to Microbial Contamination

    Eurotrol Inc. is recalling HemoTrol Level 2 hematology quality control mixtures because microbial contamination causes incorrect measurement results.

    Product
    HemoTrol Level 2- In Vitro Diagnostic Hematology quality control mixture Catalogue number: 171.002.002 Eurotrol HemoLin is an assayed hemoglobin control intended for professional use in the verification of the linearity of the HemoCue¿ Hb 201 systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0506-2019·2018-12-05

    NxStage PureFlow B Solution Recalled Due to Bag Bursting Risk

    NxStage Medical is recalling 7,275 units of PureFlow B Solution because the bag's smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-RFP-454, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0470-2019·2018-12-05

    Synaptive Medical Recalls BrightMatter Guide Software Due to Defect

    Synaptive Medical Inc is recalling 37 units of BrightMatter Guide software due to a defect that occurs when switching between specific port trajectories during surgery.

    Product
    BrightMatter Guide, Product Number SYN-0026, Versions: 1.5.0, 1.5.1 and 1.5.2 Product Usage: BrightMatter Guide can navigate a third-party port (NICO BrainPath device) by attaching Synaptive s custom Tracking Array to the port directly. As the BrainPath is navigable in two…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0720-2019·2018-12-05

    Chukar Cherry Company Recalls Ultra Dark Chocolate Amaretto Rainier Cherries

    Chukar Cherry Company is recalling Ultra Dark Chocolate Amaretto Rainier Cherries because the product contains milk, which is not listed on the label.

    Product
    Ultra Dark Chocolate Amaretto Rainier Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261 22307 7.
    Category
    Food
    Distribution
    22 states
  • SevereNHTSA·18V862000·2018-12-05

    Audi Recalls 2015-2016 A6 and A7 Models for Fire Risk

    Volkswagen is recalling 2015-2016 Audi A6 and 2015 A7 vehicles because an incorrectly inserted auxiliary heater connector may overheat and cause a fire.

    Product
    AUDI — AUDI A7, A6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0724-2019·2018-12-05

    Chukar Cherry Company Recalls Organic Chocolate Cherries for Unlabeled Milk

    Chukar Cherry Company is recalling Organic Ultra Dark Orange Chocolate Tart Cherries because the product contains milk, which is not listed on the label.

    Product
    Organic Ultra Dark Orange Chocolate Tart Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261 27207 5. The label is read in parts: "***ORGANIC ULTRA DARK ORANGE CHOCOLATE TART CHERRIES *** Ingredients: Organic Bittersweet Chocolate (Organic Cacao…
    Category
    Food
    Distribution
    22 states