The Recall Desk

State

Vermont product recalls

72,820 recalls have nationwide distribution and so reach Vermont. 1,983 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total
1,983
Critical
199
Severe
409
Most recent
2026-09-02

Of the 1,983 recalls naming Vermont we have scored against our rubric, 199 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 409 (21%) are Severe.

These figures cover only the 1,983 recalls whose distribution notice names Vermont specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

476–500 of 74803

  • SevereCPSC·26652·2026-07-30

    OCTROT heated throws and blankets recalled after 27 fires and injuries

    About 178,000 OCTROT electric throws and blankets can have their cord detach and ignite. The firm reports 555 incidents resulting in 27 fires and 15 burn or electrical shock injuries.

    Product
    OCTROT Electric Thows and Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V500000·2026-07-30

    Honda Motorcycles Recalled Due to Handlebar Lock Screw Risk

    Honda is recalling certain CMX300, CMX500, and SCL500 motorcycles because the handlebar lock screw may loosen and detach, potentially interfering with steering.

    Product
    HONDA — HONDA CMX500, CMX300, SCL500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V494000·2026-07-30

    2026 Cadillac, GMC, and Chevrolet electric vehicles recalled due to battery fire risk

    General Motors is recalling certain 2026 Cadillac Escalade, GMC Sierra EV, and Chevrolet Silverado EV models because an improperly secured battery component may increase the risk of a fire.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE IQ, ESCALADE IQL, SILVERADO EV, SIERRA EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V497000·2026-07-30

    Wanco Recalls Compact Light Towers Due to Fuel Tank Leak Risk

    Wanco is recalling 2025-2026 Compact Light Towers because the diesel fuel tank may crack and leak, increasing fire risk.

    Product
    WANCO — WANCO COMPACT LIGHT TOWER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26646·2026-07-30

    KAIFAM 5-drawer dressers recalled for tip-over and entrapment hazards

    About 1,980 KAIFAM 5-drawer metal dressers sold on Amazon are unstable when not anchored to a wall and violate the STURDY Act standard. No injuries reported.

    Product
    KAIFAM 5-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26654·2026-07-30

    Sloosh dive sticks recalled for impalement risk under federal dive stick ban

    Joyin expanded its recall of Sloosh dive sticks to models 40003 and 16154 alongside model 40041. The sticks exceed the federal compression limit and pose an impalement hazard. No injuries reported.

    Product
    Sloosh Dive Sticks, models 40041, 40003 and 16154
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V499000·2026-07-30

    Brinkley RV Recalls 2027 Model I Trailers Due to Ladder Defect

    Brinkley RV is recalling 2027 Model I trailers because the exterior ladder may not be properly secured, posing a risk of injury if it detaches.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26650·2026-07-30

    Movie souvenir cups and popcorn helmets recalled for button battery ingestion hazard

    About 55,350 Fantastic Four drinking cups and Captain America popcorn helmets with LED lights have accessible button cell batteries and lack the warning labels required by Reese's Law.

    Product
    Fantastic Four Drinking Cups and Captain America Popcorn Helmet Containers with LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26658·2026-07-30

    Woodure toddler kitchen step stools recalled after 22 tip-over reports

    About 91,000 Woodure toddler tower stools can collapse or tip over, with openings a child's torso can pass through. Woodure reports 22 incidents and 15 injuries involving scrapes, cuts and bruises.

    Product
    Woodure Toddler Kitchen Step Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26656·2026-07-30

    Baby doll playsets recalled for choking hazard under federal small parts ban

    About 1,034 Mommy's Baby Lovely Deluxe Baby Doll Playsets sold on Temu contain small parts that pose a choking hazard to children under three. No injuries reported.

    Product
    Mommy's Baby Lovely Deluxe Baby Doll Playsets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V501000·2026-07-30

    Autocar Recalls 2023-2027 ACTT Tractors Due to ABS ECU Securing Issue

    Autocar is recalling 2023-2027 ACTT terminal tractors because the ABS Electronic Control Unit may be improperly secured, potentially causing system failure and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR E-ACTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0732-2026·2026-07-29

    Cetirizine Hydrochloride Tablets Recalled Due to Cross Contamination with Ranitidine

    JB Chemicals and Pharmaceuticals Ltd is recalling 34,020 bottles of Cetirizine Hydrochloride Tablets USP 5 mg because some tablets were found to contain Ranitidine due to cross contamination.

    Product
    CETIRIZINE HYDROCHLORIDE — CETIRIZINE HYDROCHLORIDE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0719-2026·2026-07-29

    ROHTO DIGI-EYE Eye Drops Recalled Over Sterility Assurance Gap

    Rohto Digi-Eye cooling eye drops are recalled due to a lack of assurance of sterility. The recall affects 65,219 cartons distributed nationwide in the U.S.

    Product
    ROHTO DIGI-EYE — ROHTO DIGI-EYE (HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1185-2026·2026-07-29

    TNVitamins Moringa Capsules and Powder Recalled for Salmonella Contamination

    Total Nutrition Inc is recalling TNVitamins 100% Organic Moringa Capsules and Powder due to Salmonella contamination. The recall affects 8,492 units distributed nationwide.

    Product
    1. TNVitamins 100% Organic Moringa Capsules 1,200 mg 2. TNVitamins 100% Organic Moringa Powder 96 grams
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0704-2026·2026-07-29

    Major Pharmaceuticals Recalls Levothyroxine Sodium Tablets Over Subpotency

    Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 112 mcg, lot N02203, due to subpotent drug concerns. The recall affects nationwide U.S. distribution and was initiated voluntarily by the firm.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0707-2026·2026-07-29

    Levothyroxine Sodium Tablets Recalled for Subpotency

    Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 25 mcg, due to subpotency. The recall affects nationwide U.S. distribution of specific lot numbers.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0715-2026·2026-07-29

    ROHTO Cooling Eye Drops Recalled Over Sterility Assurance Concerns

    Rohto-Mentholatum (Vietnam) Co., Ltd. is recalling ROHTO Cooling Eye Drops due to a lack of assurance of sterility. The recall affects multiple lots distributed nationwide within the United States.

    Product
    Rohto Cooling Eye Drops ALL-IN-ONE (hypromellose 0.2%, tetrahydrozoline HCL 0.05%, zinc sulfate 0.25%), Sterile 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam UPC 310742010862, NDC 10742-8146-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2760-2026·2026-07-29

    FDA Recalls Power F2 Fastening Systems Over Rail Wear Risk

    The FDA is recalling 278 Power F2 Powered Fastening Systems made by Ferno-Washington Inc due to potential roller wear and rail deformation that could prevent stretcher movement.

    Product
    Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only. Designed to load, unload, and secure a compatible wheeled stretcher inside a ground-based ambulance. Item no. 0567091
    Category
    Medical Device
    Distribution
    Distributed nationwide