The Recall Desk

State

Wyoming product recalls

72,984 recalls have nationwide distribution and so reach Wyoming. 3,219 additional recalls listed Wyoming specifically in their distribution scope.

What the numbers show

Total
3,219
Critical
762
Severe
543
Most recent
2026-09-02

Of the 3,219 recalls naming Wyoming we have scored against our rubric, 762 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 543 (17%) are Severe.

These figures cover only the 3,219 recalls whose distribution notice names Wyoming specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5151–5175 of 76203

  • HighNHTSA·25V666000·2025-10-06

    Mack Trucks with Improperly Welded Seat Belt Anchorage Brackets

    Mack is recalling certain 2019-2025 MD, Anthem, Granite, and 2024 MD Electric and 2025 Pinnacle trucks with passenger bench seats. An improperly welded seat belt anchorage bracket may detach during a crash, increasing injury risk.

    Product
    MACK — MACK GRANITE (GR), MD, ANTHEM (AN), PINNACLE (PI/PN)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·031-2025·2025-10-04

    Foster Poultry Farms Recalls Chicken Corn Dogs and Ground Turkey Sticks

    Foster Poultry Farms is recalling chicken corn dogs and ground turkey on a stick products due to possible wood contamination. Consumers should not eat these items.

    Product
    Foster Poultry Farms, LLC — Foster Poultry Farms, LLC Recalls Chicken Corn Dog and Ground Turkey on a Stick Products Due To Possible Extraneous Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V663000·2025-10-03

    Altec Recalls ST600 Vehicles Due to Electrical Fire Risk

    Altec is recalling 2022-2025 ST600 vehicles with auxiliary engines because overloaded electrical circuits may overheat and increase the risk of fire.

    Product
    ALTEC — ALTEC ST600
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V664000·2025-10-03

    Recreational vehicles recalled for propane hose damage and fire hazard

    REV is recalling 2024-2026 Fleetwood Fortis and Holiday Rambler Invicta RVs with theater seats because theater seat fasteners may have damaged propane hoses, creating a fire hazard.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FORTIS, INVICTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26002·2025-10-02

    Lithium ion power banks recalled after two fires and one burn injury

    About 2,400 Kogalla power banks are being recalled after two reports of lithium-ion batteries overheating and catching fire, causing one minor burn injury and about $3,300 in property damage.

    Product
    BP125, BatPak 2F and BatPak 3F Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V659000·2025-10-02

    2024-2025 Hyundai Santa Fe starter motor terminal cover fire risk

    Hyundai is recalling 2024-2025 Santa Fe vehicles. The starter motor terminal cover may be improperly installed, causing electrical shorts that increase fire risk during crashes.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26004·2025-10-02

    Ten drawer dressers recalled for tip over and entrapment hazards

    About 610 Gunaito 10-drawer dressers sold on Walmart.com are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act stability standard.

    Product
    Gunaito 10-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V656000·2025-10-01

    2025 Toyota Tacoma Driveshaft Defect Risks Steering Failure and Rollaway

    Toyota is recalling certain 2025 Tacoma and Tacoma Hybrid vehicles because the front driveshaft CV joint may deform and break, impairing steering and risking vehicle rollaway while parked.

    Product
    TOYOTA — TOYOTA TACOMA, TACOMA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V658000·2025-10-01

    2026 Tesla Model Y: Reverse Lights May Fail to Illuminate

    Tesla is recalling certain 2026 Model Y vehicles because the reverse lights may fail to illuminate due to a wiring defect, which could reduce visibility when backing and increase crash risk.

    Product
    TESLA — TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2599-2025·2025-10-01

    Philips Brilliance iCT SP CT Systems Patient Support Table Descent

    Philips is recalling Brilliance iCT SP CT systems due to a ball screw misalignment that may cause the patient support table to descend unexpectedly to its lowest position.

    Product
    Philips CT systems labeled as the following: 1. Brilliance iCT SP, Model Number: 728311.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2635-2025·2025-10-01

    Allura CV20 systems recalled over internal component deterioration disabling motorized movement

    Philips Allura CV20 systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 46 units are affected.

    Product
    Allura CV20; Product Code: 722031; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2597-2025·2025-10-01

    Big Bore CT systems recalled because patient table may descend unexpectedly

    Philips Big Bore RT, Brilliance CT Big Bore Oncology and Brilliance CT Big Bore systems are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 33 units are affected.

    Product
    Philips CT systems labeled as the following: 1. Big Bore RT, Model Number: 728242. 2. Brilliance CT Big Bore Oncology, Model Number: 728243. 3. Brilliance CT Big Bore, Model Number: 728244.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2632-2025·2025-10-01

    Allura Xper FD20/10 systems recalled over deterioration disabling motorized movement

    Philips Allura Xper FD20/10 systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 45 units are affected.

    Product
    Allura Xper FD20/10; Product Code: 722029; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2600-2025·2025-10-01

    Ingenuity CT scanners recalled because the patient couch may descend unexpectedly

    Philips Ingenuity CT systems are recalled because the patient support table may descend unexpectedly to its lowermost position due to ball screw misalignment after a replacement. 285 units are affected.

    Product
    Philips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Number: 728321. 2. Ingenuity CT 728326, Model Number: 728323. 3. Ingenuity CT, Model Number: 728326.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2623-2025·2025-10-01

    Allura Xper FD10 systems recalled over ageing internal components stopping motorised movement

    Philips Allura Xper FD10 systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 1,117 units are affected.

    Product
    Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2608-2025·2025-10-01

    Voyant daily toric contact lenses recalled over an invalid sterilization cycle

    Voyant 1-Day Premium Toric contact lenses from one lot are recalled because the lot was manufactured with an invalid sterilization cycle. 90 units are affected.

    Product
    Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable Wear. Blister packaged.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V657000·2025-10-01

    Toyota Tundra and Sequoia Hybrid rear visibility software defect recall

    Toyota is recalling 2022-2025 Tundra, Tundra Hybrid, and 2023-2025 Sequoia Hybrid vehicles due to a software error that may prevent the rearview image from displaying when in reverse, reducing driver visibility and increasing crash risk.

    Product
    TOYOTA — TOYOTA TUNDRA HYBRID, TUNDRA, SEQUOIA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2603-2025·2025-10-01

    Ingenuity CT Brazil family recalled over patient table descending to lowermost position

    Philips Ingenuity CT Family Brazil systems, model 728325, are recalled because the patient support table may descend unexpectedly due to ball screw misalignment after a replacement. 3 units are affected.

    Product
    Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2631-2025·2025-10-01

    Allura Xper FD20/20 OR Table recalled over deteriorating internal system components

    Philips Allura Xper FD20/20 OR Table systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 3 units are affected.

    Product
    Allura Xper FD20/20 OR Table; Product Code: 722039; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
    Category
    Medical Device
    Distribution
    Distributed nationwide