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.

4176–4200 of 29102

  • SevereCPSC·24023·2023-11-09

    Twin-Star International Recalls Infrared Quartz Electric Fireplaces for Fire Hazard

    Twin-Star International is recalling approximately 14,670 Style Selections 42-inch-wide Infrared Quartz Electric Fireplaces sold at Lowe's because the units can overheat and pose a fire hazard. Twenty-four reports of overheating, fire, or smoke incidents have been received, including two reports of property damage.

    Product
    Style Selections 42-inch-wide Infrared Quartz Electric Fireplaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V754000·2023-11-09

    2024 Subaru Impreza Front Driveshaft Assembly Defect Recall

    Subaru is recalling 2024 Impreza vehicles because the front driveshaft assembly may develop cracks and break, potentially causing loss of drive power or vehicle rollaway, increasing crash risk.

    Product
    SUBARU — SUBARU FORESTER, WRX, IMPREZA, CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0308-2024·2023-11-08

    Fine Sconehenge Lemon Blueberry Scone Recall: Undeclared Egg Allergen

    Fine Sconehenge Baking Company is recalling Lemon Blueberry Scones sold through their website because they contain undeclared egg, a common allergen. Consumers with egg allergies should not consume this product.

    Product
    Fine Sconehenge Baking Company, Lemon Blueberry Scone, individually sealed plastic bag
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0310-2024·2023-11-08

    Fine Sconehenge English Scones Recalled for Undeclared Egg Allergen

    The Kitchen Garden Co, LLC is recalling Fine Sconehenge English Scones due to undeclared egg allergen. The scones, sold via the firm's website to customers in California and Nevada, may pose a risk to consumers with egg allergies.

    Product
    Fine Sconehenge Baking Company, ENGLISH SCONE, individually sealed plastic bag
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0170-2024·2023-11-08

    Senhance Robotic Surgical System uncontrolled arm motion malfunction

    Asensus Surgical recalls 21 units of Senhance Surgical System due to uncontrolled laparoscope arm motion after surgeons disengage remote control. The malfunction has occurred and may recur on affected devices.

    Product
    Senhance Surgical System, which includes: Manipulator Arm, ISU Configuration ( Catalog Number X9007708), Intelligent Surgical Unit (Catalog Number X9007696), and Cockpit, ISU Configuration (Catalog Number X9007707), Software (SW) version 2.7.4; robotic surgical system
    Category
    Medical Device
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0144-2024·2023-11-08

    Stolen McGRATH MAC Video Laryngoscopes Recalled for Failed Quality Tests

    Covidien recalls 5,709 stolen McGRATH MAC video laryngoscopes that failed quality tests. These defective devices risk failed intubation and may compromise airway management.

    Product
    Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0312-2024·2023-11-08

    Salad kit recall: Undeclared egg allergen in Wegman's Organics product

    Braga Fresh Foods is recalling Wegman's Organics Sweet Kale Chopped Salad Kit due to undeclared egg allergen. The product was distributed nationwide and may pose a risk to individuals with egg allergies.

    Product
    Wegman's Organics Sweet Kale Chopped Salad Kit, 8oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0306-2024·2023-11-08

    Chocolate Chip Scones Recalled Due to Undeclared Egg Allergen

    The Kitchen Garden Co, LLC is recalling Fine Sconehenge Baking Company Chocolate Chip Scones because they contain undeclared egg allergen. The product was misbranded and poses a risk to consumers with egg allergies.

    Product
    Fine Sconehenge Baking Company, Chocolate Chip Scone, individually sealed plastic bag
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0307-2024·2023-11-08

    Cranberry Orange Scones Recalled for Undeclared Egg Allergen

    The Kitchen Garden Co, LLC recalls Fine Sconehenge Baking Company Cranberry Orange Scones due to undeclared egg allergen. Consumers with egg allergies should not consume the product.

    Product
    Fine Sconehenge Baking Company, CRANBERRY ORANGE SCONE, individually sealed plastic bag
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0309-2024·2023-11-08

    Fine Sconehenge Lemon Raspberry Scones recalled for undeclared egg allergen

    The Kitchen Garden Co, LLC is recalling Fine Sconehenge Lemon Raspberry Scones because they contain undeclared egg. People with egg allergies could have serious reactions.

    Product
    Fine Sconehenge Baking Company, Lemon Raspberry Scone, individually sealed plastic bag
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·23V748000·2023-11-07

    Alexis Fire Equipment Recalls Fire Apparatus Due to Parking Brake Defect

    Alexis Fire Equipment is recalling 2021-2024 Fire Apparatus vehicles because a defect in the inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V746000·2023-11-07

    Mack Recalls 2024 MD Trucks Due to Steering Wheel Bolt Issue

    Mack Trucks is recalling 2024 MD trucks because the steering wheel attachment bolt may loosen and separate, potentially causing the steering wheel to detach.

    Product
    MACK — MACK MD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E086000·2023-11-07

    Cruise Recalls 950 Vehicles for Automated Driving System Software Defect

    Cruise LLC is recalling 950 vehicles because a software defect in the Collision Detection Subsystem may cause the vehicle to move after a crash.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·057-2023·2023-11-04

    Tyson Recalls Chicken Patties Due to Possible Metal Contamination

    Tyson Foods is recalling approximately 29,819 pounds of fully cooked chicken patties that may contain metal pieces. The recall affects specific lot codes distributed to nine states.

    Product
    Tyson Foods, Inc. — Tyson Foods Inc. Recalls Chicken Patty Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·23V734000·2023-11-01

    Toyota Recalls 2013-2018 RAV4 Models for Battery Fire Risk

    Toyota is recalling 2013-2018 RAV4 vehicles because certain replacement 12-volt batteries may not fit properly, potentially causing a short circuit and fire.

    Product
    TOYOTA — TOYOTA RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0300-2024·2023-11-01

    Kroger Collard Greens recalled for potential Listeria contamination

    Kroger brand collard greens packaged in 16oz bags are being recalled due to potential Listeria monocytogenes contamination. Consumers should not consume the affected product.

    Product
    Kroger Collard Greens packaged in plastic 16oz bag - 8 bags per case
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0124-2024·2023-11-01

    Infusomat Large Volume Pump False Occlusion Alarm May Interrupt Medication

    B. Braun's Infusomat Large Volume Pump battery pack may sound a false occlusion alarm, causing the device to stop pumping. This interruption of high-risk medications can lead to hemodynamic instability and serious medical consequences.

    Product
    8713052U, Infusomat Large Volume Pump, Non-Wireless BATTERY PACK; Volumetric Infusion Pump System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0302-2024·2023-11-01

    Orgain Protein Powder Recalled for Undeclared Sesame Allergen

    Orgain is recalling its Organic Protein & 50 Superfoods Protein Powder with Probiotic (chocolate flavor) due to undeclared sesame allergen. Consumers with sesame allergies are at risk of allergic reaction.

    Product
    Organic Protein & 50 Superfoods Protein Powder with Probiotic - Chocolate flavor
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Devices)·Z-0111-2024·2023-11-01

    ResMed Astral ventilators recalled for power loss and failed alarms

    ResMed recalls Astral ventilators due to a battery fault that can cause sudden power loss. The backup alarm system may fail to alert users due to supercapacitor degradation.

    Product
    Astral 100 and Astral 150 ventilators
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0067-2024·2023-11-01

    ION Sinus Spray recalled nationwide for microbial contamination

    The FDA has recalled ION Sinus Spray due to microbial contamination of the non-sterile product. All lots are affected regardless of expiration date.

    Product
    ION*Sinus Spray, 1 fl oz/ 30 mL, Manufactured by: ION* Biome Charlottesville, VA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0123-2024·2023-11-01

    B. Braun Infusomat Large Volume Pump may stop delivering medication due to false alarm

    The Infusomat Large Volume Pump may incorrectly sound an occlusion alarm and stop delivering high-risk medications, potentially causing serious complications.

    Product
    8713051U, Infusomat Large Volume Pump, Wireless; Volumetric Infusion Pump System
    Category
    Medical Device
    Distribution
    Distributed nationwide