The Recall Desk

State

Hawaii product recalls

72,968 recalls have nationwide distribution and so reach Hawaii. 2,767 additional recalls listed Hawaii specifically in their distribution scope.

What the numbers show

Total
2,767
Critical
333
Severe
567
Most recent
2026-09-16

Of the 2,767 recalls naming Hawaii we have scored against our rubric, 333 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 567 (20%) are Severe.

These figures cover only the 2,767 recalls whose distribution notice names Hawaii specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4501–4525 of 75735

  • SevereNHTSA·25V768000·2025-11-06

    GM Recalls 2019-2020 Chevrolet Silverado Medium Duty Trucks for Brake Wiring Defect

    General Motors is recalling 2019-2020 Chevrolet Silverado 4500, 5500, and 6500 trucks because a brake jumper wire harness may lack protective tape, risking power brake assist failure.

    Product
    CHEVROLET — CHEVROLET SILVERADO 6500, SILVERADO 5500, SILVERADO 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26079·2025-11-06

    Bioethanol fuel containers recalled for lacking required flame mitigation devices

    About 14,000 Y'all Can DIY bioethanol fireplace fuel containers are being recalled because they lack the flame mitigation devices required under the Portable Fuel Container Safety Act.

    Product
    Y'all Can DIY Liquid Bioethanol Fireplace Fuel Containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V763000·2025-11-06

    International Recalls 2019-2020 CV Vehicles Due to Brake Harness Defect

    International is recalling 2019-2020 CV vehicles because a brake pressure switch harness may lack protective material, potentially causing a short circuit and reduced brake performance.

    Product
    INTERNATIONAL — INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26081·2025-11-06

    WYBITNY children's bed rails recalled over multiple entrapment openings

    About 120 WYBITNY children's portable bed rails are being recalled because a child can become entrapped in the enclosed openings and in openings beside and above the mattress.

    Product
    Children's WYBITNY Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26074·2025-11-06

    Baby swings recalled for exceeding the incline limit for infant sleep

    About 1,020 Vevor baby swings are being recalled because they were marketed for infant sleep with an incline angle greater than 10 degrees, posing a suffocation risk.

    Product
    Vevor Baby Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26075·2025-11-06

    Plush alpaca toys recalled because the eyes can detach and choke

    About 64,000 Inkari plush alpaca toys are being recalled because the eyes can detach, violating the small parts ban and posing a choking hazard to children.

    Product
    Inkari Plush Alpaca Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26072·2025-11-06

    Backpack blowers recalled because the fan wheel can break apart

    About 47,800 STIHL BR 800 Magnum backpack blowers are being recalled because the fan wheel inside the blower can break apart, posing a laceration hazard.

    Product
    STIHL BR 800 Backpack Blower
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V767000·2025-11-06

    2022-2024 Toyota Tundra and Lexus LX/GX Engine Failure Recall

    Toyota is recalling certain 2022–2024 Tundra and Lexus LX/GX vehicles with V35A engines due to potential manufacturing debris contamination that can cause engine failure and loss of drive power, increasing crash risk.

    Product
    LEXUS — LEXUS, TOYOTA LX, GX, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26069·2025-11-06

    Aftermarket crib and play yard mattresses recalled over deadly entrapment gaps

    About 117,900 Criblike aftermarket play yard and non-full-sized crib mattresses are being recalled because they may not fit properly, posing a deadly entrapment hazard.

    Product
    Criblike aftermarket play yard and non-full sized crib mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0137-2026·2025-11-05

    Frozen carrot bundt cakes recalled over an undeclared wheat allergen

    Doan's Dessert And Coffee is recalling its 4 lb Carrot Bundt Cake over an undeclared wheat allergen in ready-to-eat frozen cakes. The FDA has classified the recall as Class I.

    Product
    Carrot Bundt Cake - Net Weight 4 lbs Contains: Wheat, Soy, Milk, Eggs, Tree Nuts No UPC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0138-2026·2025-11-05

    White chocolate coconut bundt cakes recalled over an undeclared wheat allergen

    Doan's Dessert And Coffee is recalling its 3 lb 12 oz White Chocolate Coconut Bundt Cake over an undeclared wheat allergen. The FDA has classified the recall as Class I.

    Product
    White Chocolate Coconut Bundt Cake - Net Weight 3 lbs 12 oz Contains: Wheat, Soy, Milk, Eggs No UPC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0163-2026·2025-11-05

    MRI operating suites recalled over ice blockage in the magnet venting system

    IMRIS is recalling the IMRIS iMRI 3T V Operating Suite because an ice blockage in the Siemens 3 Tesla magnet's venting system could rupture the helium containment system during a quench. The FDA classified it Class I.

    Product
    IMRIS Operating Suite, IMRIS iMRI 3T V, containing Siemens 3 Tesla MRI Magnet, vIDA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0164-2026·2025-11-05

    InVision operating suite recalled over ice blockage in magnet venting paths

    IMRIS is recalling the InVision 3T Operating Suite because an ice blockage in the Siemens 3 Tesla Vida magnet's venting system could rupture the helium containment system during a quench.

    Product
    IMRIS Operating Suite, InVision 3T Operating Suite, containing Siemens 3 Tesla MRI Magnet, Vida
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0162-2026·2025-11-05

    MRI operating suites with Skyra magnet recalled over venting system blockage

    IMRIS is recalling the IMRIS iMRI 3T S Operating Suite because an ice blockage in the Siemens 3 Tesla Skyra magnet's venting system could rupture the helium containment system during a quench.

    Product
    IMRIS Operating Suite, iMRI 3T S, containing Siemens 3 Tesla MRI Magnet, Skyra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0161-2026·2025-11-05

    Neuro operating suites recalled over ice blockage in magnet venting paths

    IMRIS is recalling the Neuro III-SV iMRI and iMRX systems because an ice blockage in the Siemens 3 Tesla Verio magnet's venting system could rupture the helium containment system during a quench.

    Product
    IMRIS Operating Suite, Neuro III-SV iMRI System, iMRX System, containing Siemens 3 Tesla MRI Magnet, Verio
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E073000·2025-11-05

    Bendix Recalls EC80 Electronic Control Units Due to Electrical Noise Issues

    Bendix is recalling specific EC80 Electronic Control Units because electrical noise may cause the unit to malfunction, potentially disabling critical vehicle safety systems.

    Product
    SERVICE BRAKES, AIR:ANTILOCK:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0355-2026·2025-11-05

    Mini bag spike connectors recalled over port weld separation risk

    ICU Medical is recalling 400 ChemoLock connectors with Mini Bag Spike because the port weld of the drug transfer device may separate or break during use and leak.

    Product
    ICU Medical ChemoLock w/Mini Bag Spike ¿ REF: C-17
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0338-2026·2025-11-05

    Anti-siphon smallbore extension sets recalled over port weld separation risk

    ICU Medical is recalling 950 45-inch smallbore extension sets with an anti-siphon valve because the port weld of the drug transfer device may separate or break during use and leak.

    Product
    ICU Medical 45" (114 cm) Appx 1.7 ml, Smallbore Ext Set w/Spiros w/Red Cap, Anti-Siphon Valve, Clamp, Y-Connector w/ChemoLock Port, Rotating Luer REF: CL4151
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0342-2026·2025-11-05

    Double port syringe transfer sets recalled over port weld separation risk

    ICU Medical is recalling 4,000 Double ChemoLock Port Syringe Transfer Sets because the port weld of the drug transfer device may separate or break during use and leak.

    Product
    ICU Medical Double ChemoLock Port Syringe Transfer Set REF: CL-33
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0365-2026·2025-11-05

    Chemotherapy vial adapters recalled because port weld may separate and leak

    ICU Medical is recalling 202,900 ChemosafeLock Vial Adapters because the port weld of the drug transfer device may separate or break during use and leak.

    Product
    ICU Medical ChemosafeLock Vial Adapter REFs: KL-VA001U3 KL-VA002U3 KL-VA131U3 KL-VA201U3 KL-VA202U3 KL-VA321U3
    Category
    Medical Device
    Distribution
    Distributed nationwide