The Recall Desk

State

Idaho product recalls

20,303 recalls have nationwide distribution and so reach Idaho. 0 additional recalls listed Idaho specifically in their distribution scope.

About recalls in Idaho

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Idaho consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

11301–11325 of 20303

  • HighNHTSA·23V763000·2023-11-11

    Nova Bus LFS Transit Buses Recalled for HVAC Unit Bracket Failure

    Nova Bus (US) Inc. is recalling 2020–2023 LFS transit buses because mounting brackets for the HVAC unit could fail, causing the unit to detach and create a road hazard. Free repairs are available through Nova Bus customer service.

    Product
    NOVA BUS — 2022 NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V679000·2023-11-10

    2021-2023 Tesla Model X recalled for brake fluid warning system failure

    Tesla is recalling 54,676 Model X vehicles from 2021-2023 because the vehicle controller may fail to detect low brake fluid and not display a warning light, creating a crash risk. Tesla has released a free over-the-air software update to fix the issue.

    Product
    TESLA — 2021 TESLA MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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
  • HighCPSC·24024·2023-11-09

    IKEA LETTAN Mirrors Expanded Recall Due to Laceration Hazard

    IKEA is expanding a recall of LETTAN flat mirrors because plastic wall fittings can break and cause the mirror to fall, creating a laceration hazard. No injuries have been reported.

    Product
    IKEA LETTAN Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V630000·2023-11-09

    2021-2022 Genesis vehicles fuel pump failure increases crash risk

    Hyundai is recalling certain 2021-2022 Genesis G80, GV80, and GV70 vehicles due to potential fuel pump failures that may cause loss of drive power and increase crash risk. Dealers will replace the fuel pump free of charge.

    Product
    GENESIS — 2022 GENESIS GV80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24711·2023-11-09

    Polaris RANGER XP 1000 Off-Road Vehicles Recalled for Fire and Crash Hazards

    Polaris is recalling about 1,025 Model Year 2023 RANGER XP 1000 NorthStar off-road vehicles because an improperly installed center brake line can cause overheated brakes and reduced braking performance, posing fire and crash hazards.

    Product
    Model Year 2023 RANGER XP 1000 NorthStar and XP 1000 NorthStar Crew Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24710·2023-11-09

    Magnolia Market Recalls 3-Wick Glass Candles Due to Fire and Laceration Hazards

    Magnolia Market recalled 3-Wick Glass Candles (batch 120122) due to incorrect wax causing excessive flames and glass breakage. 13 incidents reported with minor property damage in 4 cases; no injuries.

    Product
    Magnolia 26 oz. 3-Wick Glass Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24709·2023-11-09

    Arctic Cat and Tracker Side-by-Side Vehicles Recall Due to Crash Hazard

    Textron Specialized Vehicles is recalling approximately 6,800 Arctic Cat Prowler Pro and Tracker Off Road 800SX side-by-side vehicles from model years 2022 and 2023 because they can roll away while parked on an incline.

    Product
    Model Year 2022 and 2023 Arctic Cat Prowler Pro / Pro Crew and Tracker Off Road 800SX / 800SX Crew Side by Side Recreational Off Highway Vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24022·2023-11-09

    DR Power Tow-Behind Field and Brush Mowers Recalled for Fire and Burn Hazards

    DR Power Equipment and Generac are recalling approximately 2,930 tow-behind field and brush mowers because the exhaust pipe can break from excessive heat, posing fire and burn hazards. The manufacturer has received 14 reports of fires damaging the mowers.

    Product
    Tow-Behind Field & Brush Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24021·2023-11-09

    Armada, Atomic, and Salomon Ski Bindings Recalled for Fall Hazard

    Amer Sports Winter & Outdoor Company recalls certain Armada, Atomic, and Salomon ski touring bindings sold from May 2022 through September 2023 because the toe component can fail, causing the ski boot to disconnect and posing fall and injury risks.

    Product
    Armada, Atomic, and Salomon ski bindings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24712·2023-11-09

    Children's Nightgowns Recalled for Flammability Standard Violation

    iMOONZZZ children's nightgowns sold on Amazon fail to meet federal flammability standards for sleepwear, posing a burn hazard to children. About 13,300 units were sold between March and June 2023.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24713·2023-11-09

    E-Z-GO and Tracker Electric Vehicles Recalled for Unintended Movement Crash Hazard

    Textron Specialized Vehicles is recalling about 1,660 E-Z-GO ELiTE Express and Tracker OX EV vehicles because internal motor wiring damage can cause the vehicle to move unintentionally, creating a crash hazard. One incident of unexpected movement has been reported but no injuries.

    Product
    Electric Powered E-Z-GO ELiTE Express L6 and EliTE Express S6 PTV and Tracker OX EV vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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
  • HighNHTSA·23V573000·2023-11-08

    2023 Ford F-250, F-350, F-450 Rearview Camera May Not Display

    Certain 2023 Ford F-250, F-350, and F-450 trucks with the Pro Trailer Hitch Assist feature may not display the rearview camera image, reducing rear visibility and increasing the risk of a crash.

    Product
    FORD — 2023 FORD F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0208-2024·2023-11-08

    POC Analyzer Risk of Erroneous Creatinine Results During Cartridge Startup

    Nova Biomedical's Stat Profile Prime Plus POC analyzer may report inaccurate creatinine results during the first 2-4 hours after sensor cartridge installation. Standard quality control checks may not detect these errors.

    Product
    Nova Stat Profile Prime Plus POC Analyzer (CE)-Intended to measure certain gases in blood, serum, plasma or pH of blood, serum, and plasma. (1) PN 63368 Stat Profile Prime Plus POC Analyzer (2) PN 63369 Stat Profile Prime Plus POC Analyzer, Remanufactured P/N: 57400, 633
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0081-2024·2023-11-08

    Gynazole 1 Butoconazole Vaginal Cream Recalled for Formulation Error

    Padagis US LLC is recalling Gynazole 1 butoconazole nitrate vaginal cream nationwide due to a manufacturing error where hydrophilic colloidal silica was used instead of hydrophobic colloidal silica.

    Product
    GYNAZOLE 1 — GYNAZOLE 1 (BUTOCONAZOLE NITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0215-2024·2023-11-08

    Cepheid Xpert Xpress Strep A test kits may produce invalid results

    Cepheid is recalling Xpert Xpress Strep A test kits because pipettes may fail to dispense adequate sample volume, potentially resulting in invalid or absent test results.

    Product
    Xpert Xpress Strep A, XPRSTREPA-10, P/N: 302-2294 IVD, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0203-2024·2023-11-08

    Coapt Dome Electrode Gen2 System Recalled for Burn Risk

    Coapt LLC is recalling the Dome Electrode Gen2 system due to potential burns or blistering from exposure to sunlight, warm temperatures exceeding 12 hours, or battery damage.

    Product
    Coapt Dome Electrode, Gen2 system, cutaneous electrode
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0313-2024·2023-11-08

    JayRobb Vanilla Egg White Protein Powder Recalled for Plastic Contamination

    Select Custom Solutions is recalling JayRobb Vanilla Flavored Egg White Protein Powder due to plastic contamination. Approximately 1,008 pouches distributed nationwide are affected.

    Product
    JayRobb Vanilla Flavored Egg White Protein Powder. Net Weight 24 oz (1.5 lbs) 680g Dietary Supplement. UPC 6 03907-00462 3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0195-2024·2023-11-08

    Siemens Cios Alpha X-ray system software defect may cause patient misdiagnosis

    Siemens Cios Alpha (VA30) C-arm X-ray systems have a software issue that may not meet updated DIN and IEC standards. This defect could result in patient misdiagnosis or unnecessary repeat imaging.

    Product
    Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System, designed for the surgical environment. 11105200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0074-2024·2023-11-08

    FDA Recalls TUMS Antacid Tablets for Glass Mineral Wool Contamination

    GlaxoSmithKline is recalling TUMS Antacid tablets (Lot HA7G, expiration 8/31/2027) due to contamination with glass mineral wool. The product was distributed nationwide.

    Product
    TUMS — TUMS (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V636000·2023-11-08

    Indian FTR 1200 S Motorcycles Recalled for Coolant Junction Leak Risk

    Indian Motorcycle Company is recalling certain FTR 1200 and FTR 1200 S motorcycles due to a coolant junction that may leak, posing burn and crash risks to riders.

    Product
    INDIAN — 2020 INDIAN FTR 1200 S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0198-2024·2023-11-08

    RX Daytona Plus clinical chemistry analyzer may report incorrect test results

    The RX Daytona Plus clinical chemistry analyzer may report incorrect results when samples fall outside normal range and the automatic rerun feature malfunctions. Randox Laboratories is recalling 5 units distributed nationwide.

    Product
    RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number: RX4040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0196-2024·2023-11-08

    Siemens X-Ray Systems Software Issue May Cause Patient Misdiagnosis

    Siemens Medical Solutions USA is recalling 367 mobile X-ray systems (186 Cios Flow and 181 Cios Spin) due to a software issue that may result in patient misdiagnosis and repeat radiation exposure. Affected units were distributed nationwide.

    Product
    ***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray System. Designed for the surgical environment and provides comprehensive image acquisition modes. Material Number: 11108110 (2)Cios Spin- a mobile x-ray system designed to provide x-ray imaging of
    Category
    Medical Device
    Distribution
    Distributed nationwide