The Recall Desk

State

Vermont product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5201–5225 of 74923

  • ModerateFDA (Devices)·Z-2559-2025·2025-09-24

    Lactate test slides recalled over calibration failures delaying patient results

    VITROS Chemistry Products LAC Slides from coating 0130 and above are recalled because of increased calibration failures on VITROS XT systems, delaying lactate results. 2,908 units are affected.

    Product
    Chemistry Products LAC Slides. Catalog Number: 8433880. 1 Sales Unit = contains 5 cartridges of 60 slides, for a total of 300 tests.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0591-2025·2025-09-24

    L-glutamine powder recalled over unapproved drug claims on the label

    Hi-Tech Pharmaceuticals L-Glutamine Ultra Pure Powder, 500 grams, lot 059960809, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.

    Product
    HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE SIZE POWER RECOVERY ENERGY STRENGTH LACTIC ACIDE ELIMINATION LEAN MUSCLE 500 GRAMS NET WT. (17.630OZ) DIETARY SUPPLEMENT UPC 8 11836 02362 6 HI-TECH PHARMECEUTICALS, INC. 601
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Food)·H-0587-2025·2025-09-24

    Adderex XR focus tablets recalled over unapproved drug claims and misbranding

    Hi-Tech Pharmaceuticals Adderex XR, 30 tablets, lot 303120691, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.

    Product
    HI-TECH PHARMACEUTICALS ADDEREX XR STRONGEST FOCUSING AID WITHOUT A PRESECRIPTION! HELPS ADULTS MAINTAIN CONCENTRATION & IMPROVE PRODUCTIVITY! 30 TABLETS UPC 8 11836 02691 7 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-2577-2025·2025-09-24

    Twelve millimetre distraction pins recalled over unvalidated shelf life labeling

    Frontier Devices 12 mm Distraction Pins in 10 double packs are recalled because the labeling includes a shelf life that has not been validated. 160 units are affected.

    Product
    Frontier Devices, REF: 301.912S2, 12 mm Distraction Pin, 10 double packs , Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2560-2025·2025-09-24

    Lactate slides in 18-slide cartridges recalled over calibration failures delaying results

    VITROS Chemistry Products LAC Slides, catalog 8150112, from coating 0130 and above are recalled because of increased calibration failures on VITROS XT systems, delaying lactate results. 2,320 units are affected.

    Product
    VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales Unit = contains 5 cartridges of 18 slides, for a total of 90 tests.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0588-2025·2025-09-24

    Beta sitosterol supplement recalled over unapproved drug claims and misbranding

    Hi-Tech Pharmaceuticals Beta Sitosterol, 90 tablets, lot C1847, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.

    Product
    HI-TECH PHARMACEUTICALS BETA SITOSTEROL (715MG PINE DERIVED PHYTOSTEROL 99%) PROVIDES SUPPORT FOR OVERALL CARDIOVASCULAR HEALTH HELPS MAINTAIN HEALTHY CHOLESTEROL LEVELS ALREADY WITHIN THE NORMAL RANGE SUPPORTS PROSTATE AND IMMUNE HEALTH 90 TABLETS UPC 8 11836 02587 3 HI-TECH PHA
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Food)·H-0601-2025·2025-09-24

    Watermelon greens formula recalled over unapproved drug claims and misbranding

    PrimeNutrition Phytoform Fruits & Greens Formula in watermelon, 13.75 oz, lot 174271126, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.

    Product
    PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT WATERMELON NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 38302 40905 6 Manufactured by: Prime Nutrition 6015-B Unity Drive Nor
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Food)·H-0594-2025·2025-09-24

    Quercetin tablets recalled over unapproved drug claims and misbranding on label

    Hi-Tech Pharmaceuticals Quercetin, 120 tablets, lot C1612, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.

    Product
    HI-TECH PHARMACEUTICALS QUERCETIN STRENGTHENS IMMUNE SYSTEM SUPPORTS RESPIRATORY HEALTH SUPPORTS CARDIOVASCULAR HEALTH 120 TABLETS DIETARY SUPPLEMENT UPC 8 11836 02491 3 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Food)·H-0597-2025·2025-09-24

    Fruits and greens powder recalled over unapproved drug claims and misbranding

    PrimeNutrition Phytoform Fruits & Greens Formula, 13.75 oz, lot 207460659, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.

    Product
    PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT KIWI-STRAWBERRY NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 89466 70619 2 Manufactured by: Prime Nutrition 6015-b Unity Driv
    Category
    Food
    Distribution
    50 states
  • SevereNHTSA·25V635000·2025-09-23

    Blue Bird Recalls Vision Buses Due to Brake Software Defect

    Blue Bird is recalling 2021-2026 Vision school and transit buses because brake software may activate the parking brake unexpectedly, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V636000·2025-09-23

    BMW and Toyota Supra starter relays can corrode and short circuit

    BMW is recalling certain 2019-2022 BMW models and the Toyota Supra because the engine starter relay may corrode, overheat and short circuit. Owners are told to park outside until repaired.

    Product
    BMW — BMW, TOYOTA 530I, 230I, SUPRA, Z4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V634000·2025-09-23

    Porsche Cayenne, Panamera fuel pump fasteners inadequately tightened

    Porsche is recalling certain 2024–2026 Cayenne and Panamera models because fasteners securing the high pressure fuel pump may not be tightened properly, creating a fuel leak risk and potential fire hazard.

    Product
    PORSCHE — PORSCHE PANAMERA, CAYENNE, PANAMERA 4 E-HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V630000·2025-09-19

    Isuzu and Chevrolet truck fuel heaters can overheat and leak fuel

    Isuzu is recalling certain 2022-2026 FVR, FTR and Chevrolet 6500XD and 7500XD vehicles because the fuel heater may overheat, melting the casing and allowing fuel to leak into the electrical connector.

    Product
    CHEVROLET — CHEVROLET, ISUZU 7500XD, 6500XD, FVR, FTR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V628000·2025-09-19

    Ford Recalls 2020 Expedition and Lincoln Navigator for Fire Risk

    Ford is recalling 2020 Expedition and Lincoln Navigator vehicles because a short circuit in the battery junction box can cause an engine fire.

    Product
    LINCOLN — LINCOLN, FORD NAVIGATOR, EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V626000·2025-09-19

    Ford Super Duty steering column upper shaft can detach

    Ford is recalling certain 2020-2021 F-250, F-350 and F-450 vehicles because the steering column upper shaft may detach from the steering column, causing a loss of steering control.

    Product
    FORD — FORD F-450 SD, F-350 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V632000·2025-09-19

    MCI Recalls 2024-2025 Electric Coaches Due to Battery Fire Risk

    Motor Coach Industries is recalling specific 2024 and 2025 electric coaches because a high-voltage battery short circuit could cause a fire.

    Product
    MCI — MCI D45CRTELE, J4500E, D45CRTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V631000·2025-09-19

    New Flyer Recalls Transit Buses Due to High Voltage Battery Fire Risk

    New Flyer is recalling 2019-2025 XE35, XE40, and XE60 transit buses because a high voltage battery short circuit may cause a fire. Owners should park outside and limit charging to 75%.

    Product
    NEW FLYER — NEW FLYER XE35, XE40, XE60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-09192025-01·2025-09-19

    USDA Issues Public Health Alert for Trader Joe's Turkey Wrap Due to Listeria

    USDA FSIS issued a public health alert for Trader Joe's Turkey Gobbler Wraps produced on September 10, 2025, due to possible Listeria monocytogenes contamination.

    Product
    WCD Kitchen - Minooka — FSIS Issues Public Health Alert for Ready-To-Eat Turkey Wrap Product Due To Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V629000·2025-09-19

    Altec certification labels may list an incorrect axle weight rating

    Altec is recalling certain 2022-2025 Aerial Device, Forestry Body, Service Body and Digger Derrick vehicles because the Gross Axle Weight Rating on the certification label may be incorrect.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK, FORESTRY BODY, SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25468·2025-09-18

    Portable misting fans recalled after overheating while charging caused two fires

    About 22,600 IcyBreeze Buddy portable misting fans are recalled because the fan can overheat while charging and ignite. Seven overheating reports include two that resulted in fire; no injuries.

    Product
    IcyBreeze Buddy Portable Misting Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25467·2025-09-18

    Tabletop fire pits recalled because alcohol fuel can splash and flash

    About 66,000 tabletop fire pits sold at Five Below are recalled because alcohol fuel can splash or leak during use or ignition, causing a flash fire. One report of flames escaping; no injuries.

    Product
    Tabletop Fire Pits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25469·2025-09-18

    Cotton candy makers recalled after twelve reports of sparking or fire

    About 21,690 Ambiano cotton candy makers, model 836098, are recalled because the heating element can ignite sugar if used without the sugar receptacle. Twelve sparking or fire reports; no injuries.

    Product
    Ambiano Cotton Candy Makers
    Category
    Consumer Product
    Distribution
    Distributed nationwide