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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3951–3975 of 6119

  • 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
    5 states
  • SevereFDA (Devices)·Z-1138-2023·2023-03-01

    FDA Recalls NovaStar TS Standard Elbow Reusable Components for Magnet Interference Risk

    Draeger Medical is recalling 893 units of NovaStar TS Standard elbow components due to magnets that could interfere with medical devices and metallic implants.

    Product
    NovaStar TS, Standard elbow, Reusable, Material Numbers MP01579 (Size S), MP01580 (Size M), and MP01581 (Size L)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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
    5 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
    5 states
  • SevereNHTSA·23V121000·2023-02-24

    Thor Motor Coach recreational vehicles recalled for detaching overhead cabinets

    Thor Motor Coach is recalling 2018-2021 Windsport and Hurricane recreational vehicles because the driver and front passenger overhead cabinets may detach while in motion, risking injury to occupants.

    Product
    THOR MOTOR COACH — 2021 THOR MOTOR COACH WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V128000·2023-02-24

    2023 Ford Expedition front axle may fracture, increasing crash risk

    Ford is recalling certain 2023 Expeditions, along with F-150 and Lincoln Navigator vehicles, due to a front axle pinion defect that may not have been properly heat-treated. The defect can cause fracture, loss of 4-wheel drive, and wheel lockup, increasing crash risk.

    Product
    FORD — 2023 FORD EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23136·2023-02-23

    LumaRail Bed Assist Rails recalled for entrapment and asphyxia hazard

    Platinum Health is recalling about 53,000 LumaRail bed assist rails because users can become entrapped between the rail and mattress, risking death by asphyxiation. One death has been reported.

    Product
    LumaRail Bed Assist Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V120000·2023-02-23

    2022–2024 International and IC Bus Trucks/Buses: Engine Control Software Defect

    Navistar is recalling 2022-2024 International HV and MV trucks and 2022-2023 IC Bus TC buses. An engine control module software defect can cause the engine to override the parking brake when the transmission remains in drive or reverse and the power take-off switch is engaged, resulting in unintended vehicle movement.

    Product
    INTERNATIONAL — 2022 INTERNATIONAL HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0349-2023·2023-02-22

    Wegmans Asian Chop Salad Kit recalled for undeclared milk and eggs

    Wegmans Asian Chop Salad Kit may contain undeclared milk and eggs. Consumers with these allergies should not consume this product and should seek a refund or discard it.

    Product
    Wegmans Asian Chop Salad Kit Net Wt. 13 OZ (368 g) Bag code date: TFMD013A5B. UPC: 077890512838.
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·23V110000·2023-02-22

    2023 Lucid Air propulsion system electrical switches may fail unexpectedly

    Lucid is recalling certain 2022-2023 Air vehicles because electrically activated contactor switches in the propulsion system may unexpectedly open, cutting power to the electric motors and increasing the risk of a crash.

    Product
    LUCID — 2023 LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V105000·2023-02-20

    Freightliner commercial trucks recalled for drag link separation defect

    Certain 2019-2021 Freightliner commercial trucks are being recalled because the drag link taper joint may not be sufficiently tightened, potentially causing complete separation from the steering arm and total loss of steering control.

    Product
    FREIGHTLINER — 2020 FREIGHTLINER COLUMBIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V094000·2023-02-16

    Genesis Vehicles Seat Belt Pretensioners May Explode in Crashes

    Hyundai is recalling Genesis vehicles because front seat belt pretensioners may explode during a crash, potentially projecting metal fragments at occupants. Dealers will secure the pretensioners with a cap at no charge.

    Product
    GENESIS — 2021 GENESIS GV80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23126·2023-02-16

    Paradise Grills First Generation Outdoor Kitchens Recalled for Fire and Burn Hazards

    About 18,000 Paradise Grills First Generation Outdoor Kitchens are recalled because liquid propane gas can accumulate in the closed lid and cabinets, causing an explosion and severe burns when the grill is relit. Two reports of explosions causing severe burns have been received.

    Product
    Paradise Grills First Generation Outdoor Kitchens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1056-2023·2023-02-15

    GE Nuclear Medicine Imaging Systems detector fall hazard

    GE Nuclear Medicine 600/800 series imaging systems may have faulty detectors that could fall, causing serious injury. Mitigation measures may not be properly implemented on 34 units distributed worldwide.

    Product
    GE Nuclear Medicine 600/800 series systems, specifically: a) OPTIMA O640 X 3/8 inch NR, b) DISCOVERY O640 X 3/8 inch, c) NM OPTIMA O640 X 3/8 inch, d) O640 NM Gantry 3/8 inch, e) O640 NM GANTRY FINAL ASSY, f) OPTIMA O640 X 3/8 inch; Emission Computed Tomography System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1054-2023·2023-02-15

    GE Nuclear Medicine Systems: Detector Fall Risk Due to Faulty Mitigation

    GE Nuclear Medicine 600/800 series systems (748 units distributed worldwide) may have improperly implemented detector fall mitigations. If the mitigation fails, the detector can fall and cause life-threatening bodily injury.

    Product
    GE Nuclear Medicine 600/800 series systems, specifically: a) 830, b) 830 / Dismount, c) 830 /, d) 830 / 5842894-20, e) 830 / Dismount / 50HZ, f) 830 / Dismount / 60HZ, g) 830 3/8 inch Detector, h) 830 BJ, i) 830 BJ / 5144407, j) 830 BJ / Dismount, k) 830 ES DEM, l) 8
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1053-2023·2023-02-15

    GE Nuclear Medicine 600/800 Series Systems Detector Fall Risk

    GE Nuclear Medicine 600/800 series systems have a safety mitigation that may not be correctly implemented, allowing the detector to fall and cause life-threatening injury. 557 units are affected worldwide.

    Product
    GE Nuclear Medicine 600/800 series systems, specifically: a) 870, b) 870 DR 3/8 inch NM GANTRY WITH NEW ROTOR - MEA, c) 870 DR / Dismount, d) 870 DR / Dismount / 60HZ, e) 870 DR 3/8 inch WSO, f) 870 DR 3/8 inch NM Gantry, g) 870 DR 3/8 inch, h) 870 DR 3/8 inch CH, i) 8
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1057-2023·2023-02-15

    GE Nuclear Medicine Systems Recall Due to Potential Detector Fall Hazard

    GE is recalling 86 Nuclear Medicine 600/800 series systems worldwide due to a potential failure in a safety mitigation. If not correctly implemented, the detector can fall and cause life-threatening injury.

    Product
    GE Nuclear Medicine 600/800 series systems, specifically: a) 870 CZT O540+ Gantry 7.25mm, b) D670 CZT Gantry 7.25mm, c) DISCOV NM/CT 870 CZT, d) Discovery NMCT 670 CZT O540+, e) NM/CT 870 CZT CYBER DEFENCE, f) NM/CT 870 CZT O540, g) NM/CT 870 CZT WSO, h) NM/CT 870 CZT, i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1058-2023·2023-02-15

    GE Nuclear Medicine 600/800 Systems Recalled for Detector Fall Risk

    GE Medical Systems is recalling 380 GE Nuclear Medicine 600/800 series diagnostic imaging systems worldwide due to potential failure in detector mitigation that could allow the detector to fall, risking life-threatening injury.

    Product
    GE Nuclear Medicine 600/800 series systems, specifically: a) 850, b) 850 / Dismount, c) 850 3/8 inch NM Gantry, d) 860 / Dismount, e) 860 3/8 inch NM Gantry, f) 860 5/8 inch NM Gantry, g) 860 BJ, h) NM 830 3/8 inch BJ, i) NM/CT 850 3/8 inch BJ, j) NM/CT 850 3/8 inch ROW,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1055-2023·2023-02-15

    GE Nuclear Medicine BRIVO B615 Imaging System Detector Fall Risk

    GE Nuclear Medicine BRIVO B615 imaging systems may have an ineffective safety mitigation, allowing the detector to fall and cause life-threatening injury. The FDA issued a Class I recall for seven units distributed worldwide.

    Product
    GE Nuclear Medicine 600/800 series systems, specifically: a) BRIVO B615 3/8 inch DHP BJG NR, b) BRIVO 615 3/8 inch, c) BRIVO B615 3/8 inch DHP BJG NR, d) B615 with new rotor, e) BRIVO B615 3/8 inch BJG, f) BRIVO B615 3/8 inch DHP BJG NR, g) B615 with new rotor; Emissio
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0376-2023·2023-02-15

    Utopia brand Enoki Mushrooms recalled due to Listeria contamination

    Utopia brand Enoki Mushrooms (200g bags, UPC 892891861017) distributed in New York and New Jersey may be contaminated with Listeria monocytogenes. Consumers should not eat these mushrooms and should discard them or return them to the store.

    Product
    Utopia brand Enoki Mushroom; Utopia Foods Inc; 200g; Product of China; Distributed by Utopia Foods Inc.; UPC 892891861017; packaged in blue and clear plastic bag
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·23V079000·2023-02-14

    2022-2023 BMW IX and X1 driver airbag may fail to deploy in crash

    Certain 2022 and 2023 BMW IX and X1 vehicles have defective driver-side airbags that may not deploy during a crash. Dealers will replace the airbags at no charge.

    Product
    BMW — 2023 BMW IX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V073000·2023-02-10

    Freightliner Cascadia and Western Star trucks recalled for brake defect

    Daimler Trucks North America is recalling certain 2017-2023 Freightliner Cascadia and Western Star trucks. Corroded brake modulator valves may cause vehicles to pull to one side during braking, increasing crash risk.

    Product
    FREIGHTLINER — 2018 FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0246-2023·2023-02-08

    First Aid Kit with Burn Cream Recalled for Bacterial Contamination

    GFA Production is recalling Adventure First Aid 1.0 kits containing Easy Care After Burn Cream due to confirmed bacterial contamination found in FDA testing. The affected product was distributed nationwide and in Canada.

    Product
    Adventure First Aid 1.0, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 0120-0213
    Category
    Drug
    Distribution
    Distributed nationwide