The Recall Desk

State

Vermont product recalls

73,213 recalls have nationwide distribution and so reach Vermont. 2,009 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total
2,009
Critical
209
Severe
419
Most recent
2026-09-23

Of the 2,009 recalls naming Vermont we have scored against our rubric, 209 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 419 (21%) are Severe.

These figures cover only the 2,009 recalls whose distribution notice names Vermont specifically. The 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14176–14200 of 75222

  • ModerateNHTSA·23C005000·2023-11-06

    Evenflo Titan 65 Child Seat Recalled for Missing Warning Labels

    Evenflo is recalling one Titan 65 child seat because it is missing required warning labels, which may increase the risk of injury to the occupant.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V743000·2023-11-03

    Tesla Model S and Model X Incorrect Air Bag Recall

    Tesla is recalling 2021-2024 Model S and Model X vehicles because an incorrect air bag was installed when the steering wheel was replaced. The incompatible air bag could deploy incorrectly during a crash, increasing the risk of injury.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V739000·2023-11-03

    Forest River Travel Trailers Electrical Wire Gauge Defect Recall

    Forest River is recalling 2023-2024 Sandstorm, Stealth, and 2024 Shockwave travel trailers. The electrical wire from the 50-amp inlet has incorrect gauge and may melt, creating a fire hazard.

    Product
    FOREST RIVER — FOREST RIVER SANDSTORM, STEALTH, SHOCKWAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V742000·2023-11-03

    Gulf Stream Recalls 2024 Travel Trailers with Incorrect Tire Certification Labels

    Gulf Stream is recalling 2024 travel trailers because incorrect tire size and pressure information on the Federal certification label may lead to overinflation and loss of vehicle control.

    Product
    GULF STREAM — GULF STREAM FRIENDSHIP, AMERI-LITE, INDEPENDENCE, CONQUEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V737000·2023-11-02

    Freightliner M2 and 114SD Recall for Engine Lifting Bracket Defect

    Daimler Trucks North America is recalling 2024 Freightliner M2 and 114SD vehicles because an engine lifting bracket may detach, posing an injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER M2, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V735000·2023-11-02

    2023-2024 Honda Pilot steering rack defect may cause loss of steering control

    Honda is recalling certain 2023-2024 Pilot vehicles due to a loose ball bearing in the steering rack gearbox assembly. This defect can result in loss of steering control or steering lock-up, increasing crash risk.

    Product
    HONDA — HONDA PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24017·2023-11-02

    Yoocaa baby loungers recalled for suffocation and entrapment hazards

    Yoocaa baby loungers fail to meet CPSC safety requirements for infant sleep products, posing suffocation, fall, and entrapment risks. About 4,140 units sold on Amazon from January 2021 through May 2023 are affected; no injuries have been reported.

    Product
    Yoocaa baby loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24018·2023-11-02

    Lochinvar, A.O. Smith, and State Industries Condensing Boilers Recalled for Carbon Monoxide Risk

    Lochinvar LLC recalls about 17,370 residential condensing boilers sold under three brand names due to cracking flue collectors that can allow carbon monoxide emission. Consumers should contact installers for free repair or ensure working carbon monoxide alarms are installed.

    Product
    Lochinvar, A.O. Smith and State Industries brand condensing residential boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24016·2023-11-02

    Grizzly Industrial Wood Lathes Recalled for Projectile and Laceration Hazards

    Grizzly Industrial and Shop Fox wood lathes are being recalled because the cutting tool can break, creating a risk of projectiles striking users or bystanders, and lacerations to users. About 21,300 units are affected.

    Product
    Grizzly Industrial and Shop Fox Wood Lathes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24707·2023-11-02

    UncleWu Life Recalls Infant Bath Seats Due to Drowning Hazard

    UncleWu Life is recalling approximately 360 infant bath seats sold on Amazon.com from December 2020 through June 2021. The seats fail federal safety requirements and can tip over, posing a drowning hazard to infants.

    Product
    Infant Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24708·2023-11-02

    Murf Electric Bicycles Recalled for Fall and Injury Hazards

    Murf Electric Bikes is recalling about 9,000 electric bicycles sold from July 2017 through April 2022 because they do not meet U.S. safety standards and pose fall and injury hazards. The company has received one report of a fall with minor injury.

    Product
    Electric bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24019·2023-11-02

    Creativity Street Assorted Craft Buttons Recalled for Excessive Lead Content

    Dixon Ticonderoga is recalling Creativity Street Assorted Craft Buttons because they contain lead levels that exceed federal limits. Lead can cause adverse health effects if ingested by young children.

    Product
    Creativity Street Assorted Craft Buttons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0149-2024·2023-11-01

    Monoject 35 mL Syringe Recalled for Pump Incompatibility Issues

    Cardinal Health is recalling 1,097,048 Monoject 35 mL syringes due to demonstrated compatibility and recognition issues with infusion pumps. The affected units were distributed nationwide.

    Product
    Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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 (Devices)·Z-0145-2024·2023-11-01

    Monoject 1 mL Tuberculin Syringes Recalled for Infusion Pump Compatibility Issues

    Cardinal Health recalls approximately 3.1 million Monoject 1 mL Tuberculin Syringes due to demonstrated compatibility and recognition issues with syringe infusion pumps. Nationwide distribution affected.

    Product
    Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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 (Devices)·Z-0146-2024·2023-11-01

    Monoject 6 mL Syringes Recalled Due to Infusion Pump Incompatibility

    Cardinal Health is recalling Monoject 6 mL Luer-Lock syringes (approximately 3.9 million units) nationwide due to demonstrated recognition and compatibility issues with syringe infusion pumps.

    Product
    Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack
    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-0148-2024·2023-11-01

    Monoject 20 mL Syringes Recalled for Infusion Pump Compatibility Issues

    Cardinal Health is recalling 4.9 million Monoject 20 mL Luer-Lock syringes due to compatibility and recognition issues with infusion pumps. Affected lot numbers from 2022 and 2023 were distributed nationwide.

    Product
    Monoject 20 mL Syringe Luer-Lock Tip Soft Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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