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.

2626–2650 of 29088

  • SevereFDA (Devices)·Z-0081-2025·2024-10-30

    Anesthesia Machine Recall Due to Patient Breathing Circuit Misconnection Risk

    Datex-Ohmeda Aisys anesthesia machines may allow patient breathing circuits to be incorrectly connected to the Auxiliary Common Gas Outlet, potentially affecting ventilation during anesthesia. Approximately 4,790 units worldwide are affected.

    Product
    Aisys. This anesthesia gas machine is intended to provide general inhalation anesthesia and ventilatory support to patients and are to be used only by medical professionals trained and qualified in the administration of general anesthesia.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0082-2025·2024-10-30

    Aisys CS2 Anesthesia Machine Recall: Breathing Circuit Misconnection Risk

    Datex-Ohmeda is recalling approximately 15,739 Aisys CS2 anesthesia machines worldwide. A breathing circuit limb may be mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port instead of the intended connection point.

    Product
    Aisys CS2. This anesthesia gas machine is intended to provide general inhalation anesthesia and ventilatory support to patients and are to be used only by medical professionals trained and qualified in the administration of general anesthesia.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0078-2025·2024-10-30

    Anesthesia Gas Machine Recall: Breathing Circuit Misconnection Risk

    Datex-Ohmeda is recalling Avance anesthesia gas machines worldwide due to a potential hazard if a patient's breathing circuit is incorrectly connected to the Auxiliary Common Gas Outlet port during setup.

    Product
    Avance. This anesthesia gas machine is intended to provide general inhalation anesthesia and ventilatory support to patients and are to be used only by medical professionals trained and qualified in the administration of general anesthesia.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·029-2024·2024-10-29

    A Tu Gusto Recalls Frozen Croquettes for Undeclared Allergens and Lack of Inspection

    A Tu Gusto, LLC is recalling approximately 7,630 pounds of frozen croquette products that were produced without federal inspection and contain undeclared allergens.

    Product
    A Tu Gusto, LLC Recalls Frozen Croquette Products Produced Without the Benefit of Inspection and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·24V809000·2024-10-28

    Porsche Recalls 2021-2024 Models for Wheel Bolt Fracture Risk

    Porsche is recalling 2,251 vehicles because a center lock wheel bolt may fracture, causing the wheel to detach and increasing crash risk.

    Product
    PORSCHE — PORSCHE 911, 718 CAYMAN GT4 RS, 718 SPYDER RS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V805000·2024-10-25

    Ford Recalls 2023-2024 Transit Vehicles for Rear Axle Bolt Defect

    Ford is recalling 2023-2024 Transit vehicles previously repaired under recall 24V-102 because incorrect rear axle shaft bolts may cause wheel lock-up or separation.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V797000·2024-10-24

    GM diesel transmission control valves may fail and lock rear wheels

    GM is recalling certain 2020-2022 diesel Silverado, Sierra, Escalade, Tahoe, Suburban and Yukon vehicles because the transmission control valve may fail and cause rear wheel lock-up.

    Product
    GMC — GMC, CHEVROLET, CADILLAC SIERRA 1500, SILVERADO 3500, TAHOE, SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E090000·2024-10-24

    Reading Truck Equipment Recalls Curt Trailer Hitches on Ford Trucks

    Reading Truck Equipment is recalling 116 Curt trailer hitches installed on 2023-2024 Ford F350 and F550 vehicles because fuel tank straps were not properly tightened.

    Product
    FUEL SYSTEM, DIESEL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25021·2024-10-24

    Ricky Powersports ATVs Recalled for Safety Regulation Violations

    Ricky Powersports is recalling about 385 youth and adult all-terrain vehicles due to violations of federal ATV safety regulations that pose risks of serious injury or death. The youth ATVs have suspension defects, and the adult ATVs have brake and handlebar safety issues.

    Product
    Ricky Powersports Tumble Weed Youth and TGB Blade Adult All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V796000·2024-10-24

    Inspire Recalls 2024 Newport Trailers Due to Cooktop Fire Risk

    Inspire RVs is recalling 2024 Newport 27 and 29 trailers because a cooktop circuit board may overheat and cause a fire. All affected units were repaired in September 2024.

    Product
    INSPIRE — INSPIRE NEWPORT 27, NEWPORT 29
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E089000·2024-10-23

    Silver Eagle Recalls Eye and Shank Assemblies Due to Weld Fatigue

    Silver Eagle is recalling specific eye and shank assemblies because welds may crack, allowing the eye to separate from the trailer converter dolly and increasing crash risk.

    Product
    STRUCTURE:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0048-2025·2024-10-23

    GE HealthCare Recalls Giraffe OmniBed Carestations Due to Door Screw Issue

    GE HealthCare is recalling certain Giraffe OmniBed Carestations because a screw securing the heater doors may not be torqued to specification, potentially causing the doors to become loose.

    Product
    GE Heathcare Giraffe OmniBed Carestation, Model Number 2082844-001-XXX; neo natal incubator
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0036-2025·2024-10-23

    Enjoy Premium Coconut Cookies Recalled for Undeclared Milk Allergen

    KTM Services, Inc. is recalling Enjoy Premium Coconut Cookies sold in Hawaii, Guam, Nevada, and online due to undeclared milk allergen. Consumers with milk allergies should not consume the product.

    Product
    Enjoy Premium Coconut Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear bags
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0046-2025·2024-10-23

    Octopus Product Recalled for Undeclared Fish Allergen

    Lemonland Food Corp is recalling Item FLD2011 Salted and Seasoned Small Octopus because it contains undeclared fish (anchovy), a major allergen. Approximately 70 packages were distributed in Washington state.

    Product
    Item FLD2011, Salted and Seasoned Small Octopus, distributed in plastic clamshell containers, net wt. 0.267lb. The H-Mart label declares: Octopus, Salt, Garlic, Ginger, Red Pepper Powder, Green Onion, Syrup, Sesame Seed.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0035-2025·2024-10-23

    Enjoy Premium Taro Cookies recalled for undeclared milk allergen

    Enjoy Premium Taro Cookies contain undeclared milk allergen and were sold in Hawaii, Guam, and Nevada. Consumers with milk allergies should not consume this product.

    Product
    Enjoy Premium Taro Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear bags
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0048-2025·2024-10-23

    Seasoned Pepper with Soybean Paste Recalled for Undeclared Allergens

    Lemonland Food Corp is recalling Item FLD1020A Seasoned Pepper with Soybean Paste due to undeclared wheat, fish, and crustacean allergens. Consumers with allergies should not consume this product.

    Product
    Item FLD1020A, Seasoned Pepper with Soybean Paste, distributed in plastic clamshell containers. Net wt. 0.315lb. The H-Mart label declares: Pepper, Soy Bean Paste.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0044-2025·2024-10-23

    Seasoned Dandelion Recalled for Undeclared Fish Allergen

    Lemonland Food Corp is recalling Item FLD1070A Seasoned Dandelion due to undeclared fish (anchovy) not listed on the label. Consumers with fish allergies should not consume this product.

    Product
    Item FLD1070A, Seasoned Dandelion, distributed in plastic clamshell containers. Net wt. 0.365lb. The H-Mart label declares: Dandelion, Salt, Garlic, Soy Sauce, Chili Powder.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0041-2025·2024-10-23

    Perilla Leaves in Soy Sauce recalled for undeclared wheat and fish allergens

    Lemonland Food Corp recalls Item FLD1000BA Perilla Leaves in Soy Sauce due to undeclared wheat and fish allergens on the label. Consumers with these allergies should not consume the product.

    Product
    Item FLD1000BA, Perilla Leaves in Soy Sauce, distributed in plastic clamshell containers, net wt. 0.315lb. The H-Mart label declares: Perilla Leaves, Soy Sauce, Sugar
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0047-2025·2024-10-23

    GE HealthCare Giraffe OmniBed neonatal incubator door screw may loosen

    Certain GE HealthCare Giraffe OmniBed and Carestation neonatal incubators may have door-securing screws that were not torqued to specification, potentially causing the doors to become loose. These units are distributed worldwide.

    Product
    GE Heathcare Giraffe OmniBed; neo natal incubator
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0038-2025·2024-10-23

    Potato Salad Recall: Undeclared Egg and Soybean Allergens

    Lemonland Food Corp is recalling potato salad due to undeclared egg and soybean allergens present in the mayonnaise ingredient. The recall affects 120 packages distributed in Washington.

    Product
    Item FLD4006, Potato Salad, distributed in plastic clamshell containers, net wt. 0.56lb. The H-Mart label declares: Potato, Mayonnaise, Sugar, Vegetable.
    Category
    Food
    Distribution
    1 state