The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

5626–5650 of 29102

  • SevereFDA (Devices)·Z-1142-2023·2023-03-08

    Life2000 Ventilator poses oxygen desaturation risk with oxygen concentrators

    The FDA recalls Baxter's Life2000 Ventilator due to potential patient desaturation when connected to an oxygen concentrator. Affects 71 units nationwide.

    Product
    Life2000 Ventilator , REF MS-01-0118, ventilatory support for the care of individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1140-2023·2023-03-08

    Life2000 Hospital Ventilator Recalled for Potential Patient Desaturation Risk

    Baxter Healthcare is recalling 135 Life2000 ventilators nationwide due to potential patient desaturation when connected to an oxygen concentrator.

    Product
    Life2000 Ventilator PKG, Hospital, a) REF BT20007, b) REF BT-20-0007, ventilatory support for the care of individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1139-2023·2023-03-08

    Life2000 Ventilator System Recall: Risk of Patient Desaturation

    Baxter Healthcare is recalling 4,279 Life2000 Ventilator Systems due to potential patient desaturation when connected to oxygen concentrators.

    Product
    Life2000 Ventilator System, a) REF BT-20-0002, b) REF BT-20-0002A, ventilatory support for the care of individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V154000·2023-03-08

    2023-2024 International trucks recalled for loose battery box bolts

    Navistar is recalling certain 2023 and 2024 International trucks because battery box mounting bolts may be loose or missing. Loose bolts could allow the battery box to detach, creating a road hazard and increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL MV, HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V155000·2023-03-08

    Ford Recalls 2022-2023 Bronco for Steering Gear Lock-Up Defect

    Ford recalls 2022-2023 Broncos for steering gear damage that can lock up the steering wheel and cause loss of steering control, increasing crash risk.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V148000·2023-03-07

    Terex Advance Front Discharge Mixer Recall for Loose Axle Fasteners

    Terex Advance is recalling 2022 Front Discharge Mixer Commander vehicles because front-drive steer axle fasteners may not be tightened sufficiently, risking axle separation and loss of control.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V147000·2023-03-06

    Newell Recalls 2023-2024 P50 Motor Coaches Due to Brake Light Defect

    Newell Coach Corp. is recalling 2023-2024 P50 motor coaches because brake lights may fail to illuminate unless the brake pedal is fully depressed, increasing crash risk.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·007-2023·2023-03-06

    Dahlia Imports Recalls Raw Bone-in Goat Products Lacking USDA Inspection

    Dahlia Imports is recalling approximately 196,019 pounds of raw bone-in goat products imported from Australia without the required USDA import reinspection.

    Product
    Dahlia Imports, LLC Recalls Raw Bone-in Goat Products Imported Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·23V145000·2023-03-03

    Xos Recalls 275 Vehicles Due to Driveshaft Bolt Tightening Defect

    Xos is recalling 275 RM01, SA01, and SV05 vehicles because improperly tightened bolts may allow the driveshaft to separate, increasing crash risk.

    Product
    XOS — XOS RM01, SV05, SA01
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23C002000·2023-03-03

    Dorel Recalls Multiple Child Seat Models Due to Anchor Failure Risk

    Dorel Juvenile Group is recalling specific Safety 1st and Maxi-Cosi child seats because lower anchors may fail, allowing the seat to detach in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V137000·2023-03-02

    Land Rover Recalls 2023 Defender 130 for Third-Row Seat Latch Defect

    Jaguar Land Rover is recalling 2023 Defender 130 vehicles with third-row seats because the seatback latch may not secure child seat tethers properly, increasing crash injury risk.

    Product
    LAND ROVER — LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0372-2023·2023-03-01

    TOHATO Nagewa Seaweed Snack Recalled for Unlisted Milk and Shellfish Allergens

    TOHATO Nagewa Snack Seaweed Flavor contains undisclosed milk and shellfish allergens. The product is distributed to Daiso stores in CA, WA, Nevada, TX, NY, and NJ; consumers with these allergies should not consume.

    Product
    TOHATO Nagewa Snack Seaweed Flavor 71g units UPC:4901940112012
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0368-2023·2023-03-01

    TOHATO Caramel Corn Recalled for Undeclared Almonds

    TOHATO Caramel Corn products sold at Daiso stores are being recalled because almonds are present but not listed on the ingredient label, posing risk to people with almond allergies.

    Product
    TOHATO Caramel Corn - 80g units - UPC:4901940111107 2pieces TOHATO Caramel Corn - 23g units - UPC:4901940111138 TOHATO Caramel Corn 4 continuous pack - 40g units - UPC:4901940111152 TOHATO Bitter Caramel Corn - 77g units - UPC:4901940111121
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0366-2023·2023-03-01

    Caramel Corn Boys Festival recalled for undeclared almonds and peanuts

    Caramel Corn Boys Festival snack packs, distributed to Daiso stores, contain undeclared almonds and peanuts. This creates serious health risks for consumers with nut allergies.

    Product
    Caramel Corn Boys Festival 80g units UPC:4901940039432
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0369-2023·2023-03-01

    TOHATO Bitter Caramel Corn Snack Recalled for Undisclosed Almond Allergen

    TOHATO Bitter Caramel Corn 77g units are recalled because they contain almonds not listed on the ingredient label. This poses a serious risk to consumers with almond allergies.

    Product
    TOHATO Bitter Caramel Corn 77g units UPC:4901940111121
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0381-2023·2023-03-01

    KANRO Pure Gummy Candy Recalled for Undeclared Soy Allergen

    KANRO Pure gummy candies are being recalled due to undeclared soy allergen on the label. The recall affects 113,205 units sold at Daiso stores across multiple states and Canada.

    Product
    KANRO Pure gummy Petit trigonal pyramid grape 17g 3 pieces UPC: 4901351055489
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0379-2023·2023-03-01

    ITOSEIKA Chocolate Chip Cookies Recalled for Undeclared Milk Allergen

    DAISO CALIFORNIA WAREHOUSE is recalling ITOSEIKA Chocolate Chip Cookies due to undeclared milk allergen on the label. Products were distributed to Daiso stores in California, Washington, Nevada, Texas, New York, New Jersey, and British Columbia.

    Product
    ITOSEIKA Chocolate chip cookies 10pieces UPC: 4901050137172
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0367-2023·2023-03-01

    Caramel Corn The Star Festival Recalled Due to Undeclared Almonds

    Caramel Corn The Star Festival 80g units are recalled because they contain almonds that are not listed on the ingredient label. About 317,751 units were distributed to Daiso stores in six U.S. states and Canada.

    Product
    Caramel Corn The Star Festival 80g units UPC:4901940039647
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0380-2023·2023-03-01

    Katoseika Chocolat Orange Candy recalled for undeclared soy allergen

    Daiso California Warehouse is recalling Katoseika Chocolat Orange Candy (60g) due to undeclared soy allergen. The product was distributed to Daiso stores across multiple U.S. states and Canada.

    Product
    Katoseika Chocolat Orange Candy 60g UPC: 4901580002315
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0361-2023·2023-03-01

    Pilgrim's Roasted Nut'Z English Toffee Peanuts recalled due to undeclared milk

    Pilgrim's Roasted Nut'Z English Toffee Peanuts (580 packages) are recalled because the label does not declare the presence of milk. Consumers with milk allergies should not consume this product.

    Product
    Pilgrim's Roasted Nut'Z English Toffee Peanuts are packaged by hand into either the 8 oz Plastic Cone Bags or 8 Oz Pouch Bags. Label declares Spanish peanuts, sugar, English Toffee Syrup.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0377-2023·2023-03-01

    MEITO Powdered Apple Tea recalled for undeclared milk allergen

    DAISO CALIFORNIA WAREHOUSE is recalling MEITO Powdered Apple Tea 4packs because the product contains milk that is not declared on the label. Consumers with milk allergies should not consume this product.

    Product
    MEITO Powdered Apple Tea 4packs UPC: 4902757413606
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0378-2023·2023-03-01

    Daiso Potato Crackers with Sardines Recalled for Undeclared Milk

    Daiso potato crackers with sardines (46g) are being recalled due to undeclared milk allergen. The product was distributed across six US states and parts of Canada.

    Product
    Potato crackers with small sardines 46g UPC: 4901053077376
    Category
    Food
    Distribution
    6 states