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 deaths or serious injuries are reported, 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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5226–5250 of 36551

  • SevereFDA (Food)·F-1638-2023·2023-10-04

    Heaven Layer Ice Cream Recalled Due to Listeria Monocytogenes Contamination

    Heaven Layer ice cream products have been recalled due to possible Listeria monocytogenes contamination. The products were distributed in Ohio, New Jersey, and New York.

    Product
    Heaven Layer Vanilla / Strawberry / Mocha / Vanilla; parve ; 1 PACK; UPC: 0-91404-15184-9
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1693-2023·2023-10-04

    Premium Sorbet Recall Due to Listeria Contamination Risk

    Ice Cream House is recalling Premium Sorbet Quart (Blueberry Lime) distributed in Ohio, New Jersey, and New York due to possible Listeria monocytogenes contamination.

    Product
    Premium Sorbet Quart / Blueberry Lime; parve; 1 PACK; UPC: 0-91404-15162-7
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1658-2023·2023-10-04

    Cigar Shells Recalled Due to Listeria Contamination Risk

    Ice Cream House is recalling Cigar Shells due to potential Listeria monocytogenes contamination. Affected products distributed in Ohio, New Jersey, and New York should not be consumed.

    Product
    Cigar Shells; dairy / parve; 6 PACK / SINGLE; UPC: 0-91404-15130-6
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·23V668000·2023-10-03

    Volvo Bus Recalls 2023 9700 Models Due to Power Cable Fire Risk

    Volvo Bus is recalling 2023 9700 vehicles because power cable fasteners may not be tightened securely, which can cause overheating and increase the risk of a fire.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E073000·2023-10-02

    Mando ABS Module Recall for Engine Compartment Fire Risk

    Mando America Corporation is recalling ABS modules that may leak brake fluid and cause electrical shorts, leading to engine compartment fires.

    Product
    SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23299·2023-09-29

    Future Motion Onewheel Electric Skateboards Recalled for Crash Hazard

    Future Motion is recalling approximately 300,000 Onewheel self-balancing electric skateboards because they can stop balancing and cause the rider to crash. Four deaths and dozens of injuries including head trauma, fractures, and paralysis have been reported.

    Product
    Onewheel Electric Skateboards (all models)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V655000·2023-09-28

    Diamond C Trailers Recall 2023-2024 Models Due to Winch Failure

    Diamond C is recalling 2023-2024 FMAX, SDX, and PX trailers because the spare tire winch may loosen or fail, increasing crash risk.

    Product
    DIAMOND C TRAILERS — DIAMOND C TRAILERS FMAX, PX, SDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V656000·2023-09-28

    Autocar Recalls Xpeditor and Legend Vehicles for Steering Defect

    Autocar is recalling 2022-2023 Xpeditor and 2023 Legend vehicles because a steering column bolt may not be secured, risking sudden loss of steering.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2530-2023·2023-09-27

    Ventilator Spare Parts Recalled for Degrading Capacitor Risk

    Hamilton Medical is recalling ventilator spare parts (ESM Shielding Set) due to potentially degrading capacitors on the control board. These capacitors may leak electrolyte and cause a short circuit, interrupting ventilation.

    Product
    Hamilton-T1, REF: MSP161339/02, ESM Shielding Set, Spare Part for ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1174-2023·2023-09-27

    Novartis Withdraws SANDIMMUNE Oral Solution Bottles Due to Crystallization

    Novartis is recalling SANDIMMUNE Oral Solution bottles nationwide because they were found to contain crystals. Patients should contact their pharmacy or prescriber about affected bottles.

    Product
    SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue S.A.S., Huningue, France, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936, NDC 0078-0110-22.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2525-2023·2023-09-27

    Portable Intensive Care Ventilator Recalled for Degrading Capacitor Issue

    Hamilton Medical is recalling 164 Hamilton-C1 portable ventilators due to degrading capacitors that may leak electrolyte, causing electrical short circuits that could interrupt ventilation.

    Product
    Hamilton-C1, REF: 161001, Portable Intensive Care Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2528-2023·2023-09-27

    Intensive Care Ventilators Recalled Due to Capacitor Degradation Risk

    Hamilton Medical is recalling 12 intensive care ventilators (model Hamilton-MR1) due to degrading capacitors that may leak electrolyte, potentially causing ventilation interruption. The recall affects specific serial numbers across the US and Puerto Rico.

    Product
    Hamilton-MR1, REF: 161010, Intensive Care Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1544-2023·2023-09-27

    Dietary Supplement Capsules Recalled for Toxic Yellow Oleander Substitution

    OBC GROUP CORP is recalling NUT DIET MAX dietary supplement capsules due to substitution with toxic Yellow Oleander instead of the labeled ingredient Nuez de la India.

    Product
    NUT DIET MAX, Nuez de la India, Aleurites Moluccanus, 30 Capsules, 500mg Veggie Caps
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2529-2023·2023-09-27

    Ventilator Control Board Spare Parts Recalled Due to Electrical Short-Circuit Risk

    Hamilton Medical is recalling 6 control board spare parts for ventilators due to degrading capacitors that may leak electrolyte and cause electrical short circuits, potentially interrupting ventilation.

    Product
    Hamilton C1/T1/MR1, REF: MSP161502/12, Control Board Spare part for ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2527-2023·2023-09-27

    Hamilton-T1 Ventilator Recall: Degrading Capacitors May Interrupt Ventilation

    Hamilton Medical recalls 1,216 Hamilton-T1 ventilators due to degrading capacitors on the control board that may leak electrolyte and interrupt ventilation. The recall affects units distributed nationwide in the US and Puerto Rico.

    Product
    Hamilton-T1, REF: 161009, Intensive Care and Transport Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·046-2023·2023-09-25

    USDA Recalls Ineligible Imported Pork Chicharrones from Honduras

    Del Valle Import and Export is recalling 1,271 pounds of pork chicharrones imported from Honduras, a country ineligible to export pork to the U.S.

    Product
    Del Valle Import and Export, LLC, Recalls Ineligible Pork Chicharrones Product Imported From Honduras
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·23V652000·2023-09-25

    Kia Recalls Multiple Models Due to Electrical Short Fire Risk

    Kia is recalling 1.7 million vehicles because an electrical short in the brake control unit may cause an engine compartment fire.

    Product
    KIA — KIA SORENTO, RIO, OPTIMA HYBRID, SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V651000·2023-09-22

    Hyundai Recalls Multiple Models Due to ABS Module Fire Risk

    Hyundai is recalling over 1.6 million vehicles because a leaking ABS module may cause an engine compartment fire. Owners should park outside until the repair is complete.

    Product
    HYUNDAI — HYUNDAI ELANTRA, AZERA, SANTA FE, GENESIS COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23290·2023-09-21

    HONEY JOY Infant Swings Recalled for Suffocation Hazard

    HONEY JOY infant swings are recalled due to a suffocation hazard. The product violates federal safety standards because it has an incline angle greater than 10 degrees and was marketed for infant sleep, and infant fatalities have been reported in similar inclined sleepers.

    Product
    HONEY JOY Infant Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V647000·2023-09-21

    2023 Subaru Driveshaft Center Support Bolts May Loosen

    Subaru is recalling certain 2023 Ascent, Legacy, Impreza, and Outback vehicles because center support bolts for the driveshaft may loosen, potentially causing the driveshaft to disconnect and increasing crash risk. Dealers will clean and replace the bolts at no charge.

    Product
    SUBARU — SUBARU OUTBACK, ASCENT, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide