The Recall Desk

State

Hawaii product recalls

72,940 recalls have nationwide distribution and so reach Hawaii. 2,766 additional recalls listed Hawaii specifically in their distribution scope.

What the numbers show

Total
2,766
Critical
333
Severe
567
Most recent
2026-09-09

Of the 2,766 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 2,766 recalls whose distribution notice names Hawaii specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4176–4200 of 75706

  • HighFDA (Devices)·Z-0601-2026·2025-12-03

    Brain access devices recalled because packaging tape contains latex

    Stryker is recalling 39,148 NICO BrainPath devices because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.

    Product
    NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde; NN-8042 BrainPath Shephard's Hook - Greenberg LK;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0588-2026·2025-12-03

    Heated massage tables recalled over heat components that can smolder

    Pivotal Health Solutions is recalling 464 Quantum Intersegmental Tables because damage to the heat function components can lead to overheating, smoldering and melting of the vinyl cushion.

    Product
    Quantum Intersegmental Table, Model/Catalog Number: AMQ400H; heated massage table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0600-2026·2025-12-03

    Illumination packs recalled because packaging tape contains undisclosed latex

    Stryker is recalling 39,148 NICO Myriad Illumination Packs because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.

    Product
    NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/Fiber
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0578-2026·2025-12-03

    IV set 490487 recalled over piggyback backflow and occlusion risk

    B. Braun Medical is recalling 23,160 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    FoundationOne Liquid CDx (F1LCDx), TECH-0009 version 6.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0720-2026·2025-12-03

    Anesthesia vaporizers recalled over the potential for anesthesia leakage

    Mindray is recalling 148 Sevoflurane V90 Electronic Vaporizers used with the A9 Anesthesia System over the potential for anesthesia leakage.

    Product
    Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap. (Safety Filling adapter), Part Number: 115-066756-00. 2. Exchange Sev E_Vap. (Safety Filling adapter), Part Number: E115-066756-00. Product Description: Th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0719-2026·2025-12-03

    Interventional imaging systems recalled over ceiling rail movement that may fail

    Philips is recalling 172 Azurion 7M20 systems with FlexArm because motorized longitudinal movement of the stand may be inconsistent and eventually become unavailable.

    Product
    Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-0585-2026·2025-12-03

    Culture media recalled over contamination that may darken the broth

    Remel is recalling cation-adjusted Mueller Hinton broth and Brucella broth because the products may contain contamination, which may result in a darker or brown media color.

    Product
    1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0581-2026·2025-12-03

    Vitrectomy probe packs recalled with no reason stated in the record

    Alcon Research is recalling 28,323 Constellation UltraVit 10K and HyperVit 20K vitrectomy probe packs; the enforcement record does not state a reason.

    Product
    CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/ 8065000093; 25+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000095; 27+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000096; 23GA BEVEL ULTRAVIT 10,000 CPM/ 8065752413; 25+ B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V834000·2025-12-02

    Zero Recalls 2023 DSR/X Motorcycles Due to Motor Controller Defect

    Zero Motorcycles is recalling 2023 DSR/X motorcycles because incorrect fasteners in the motor controller may cause a loss of drive power, increasing crash risk.

    Product
    ZERO — ZERO DSR/X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V827000·2025-12-01

    Ford Recalls 2016-2019 Lincoln MKT for Detaching B-Pillar Trim

    Ford is recalling 2016-2019 Lincoln MKT vehicles because the B-pillar door trim may detach while driving, creating a road hazard and increasing crash risk.

    Product
    LINCOLN — LINCOLN MKT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V828000·2025-12-01

    Ford Recalls 2025 Maverick for Cylinder Head Manufacturing Defect

    Ford is recalling 2025 Maverick vehicles with defectively manufactured cylinder heads that can leak oil. The leak increases the risk of fire and engine failure.

    Product
    FORD — FORD, LINCOLN EXPLORER, MUSTANG, MAVERICK, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V824000·2025-12-01

    2019 Ram Trucks Recalled for Side Curtain Air Bag Inflator Defect

    Chrysler is recalling 2019 Ram 1500, 2500, and 3500 vehicles because side curtain air bag inflators may rupture, potentially sending metal fragments into the cabin.

    Product
    RAM — RAM 1500, 2500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V832000·2025-12-01

    Virnig Recalls 2025 Trailers Due to Bearing Lock Nut Failure Risk

    Virnig is recalling 2025 TR-HDD-1414 and TR-RHDD-1409 trailers because improperly installed bearing lock nuts may fail, causing the tire to detach and increasing crash risk.

    Product
    VIRNIG — VIRNIG TR-RHDD-1409, TR-HDD-1414
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V833000·2025-12-01

    Genesis G90 Models: Highway Drive Assist Braking Malfunction Recall

    Hyundai is recalling 2023-2026 Genesis G90 vehicles because the Highway Drive Assist radar may falsely detect another vehicle, causing sudden braking that increases crash risk.

    Product
    GENESIS — GENESIS G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V826000·2025-12-01

    2025-2026 RAM Pickup Trucks: Blank Instrument Panel Display Software Error

    Chrysler is recalling 2025-2026 RAM pickup trucks (1500, 2500, 3500, 4500, 5500) because a software error causes the instrument panel display to go blank, preventing drivers from seeing critical warning lights and gear selection.

    Product
    RAM — RAM 1500, 2500, 3500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V831000·2025-12-01

    2025 Lincoln Navigator Rear Lightbar Cracks May Disable Reverse Lights

    Ford is recalling certain 2025 Lincoln Navigator vehicles. The rear lightbar may develop cracks allowing moisture accumulation, potentially disabling reverse lights and reducing visibility when backing up.

    Product
    LINCOLN — LINCOLN NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V829000·2025-12-01

    2025 Ford Escape liftgate hinge covers may detach, creating crash risk

    Ford is recalling certain 2025 Escape vehicles because liftgate hinge covers may not be properly secured and can detach. Detached covers can create a distraction or road hazard, increasing crash risk.

    Product
    FORD — FORD ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V823000·2025-12-01

    2025 Ford Expedition and Other Models Recalled for Brake Booster Malfunction

    Ford is recalling 679 2025 Expedition, Ranger, F-150, Bronco, and Navigator vehicles due to a potential Electronic Brake Booster malfunction that can cause loss of power brake assist, increasing crash risk.

    Product
    FORD — FORD, LINCOLN F-150, EXPEDITION, BRONCO, RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V825000·2025-12-01

    KTM and Husqvarna motorcycles recalled for engine control software stalling defect

    KTM and Husqvarna are recalling certain 2024-2025 motorcycles because faulty engine control software may cause the engine to stall at low RPMs, creating a risk of crashes.

    Product
    KTM — KTM, HUSQVARNA 390 SMC R, 390 ENDURO R, 390 ADVENTURE X, VITPILEN 401
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V822000·2025-11-28

    Nova Bus Recalls LFS Transit Buses Due to Cooling Pump Defect

    Nova Bus is recalling 2021 and 2024-2025 LFS transit buses because a loose impeller shaft may cause the cooling pump to fail, potentially leading to a loss of drive power and increased crash risk.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0430-2026·2025-11-26

    Infusion pump modules recalled because drops can damage the bezel assembly

    CareFusion is recalling 2,574,396 BD Alaris Infusion Pump Modules 8100 because a dropped or jarred pump can suffer bezel damage causing under-infusion, over-infusion or unregulated flow.

    Product
    BD Alaris infusion Pump Module 8100, REF: 8100; KIT, BEZEL ASSY 8100BD, REF: 49000437; KIT ASSY ONE PIECE BEZEL 8100, REF: 49000270. Used with the following new and updated documents: BD Alaris Infusion System Inspection Safety Reminder, Part: BD-163124, Revision: 00; Clean
    Category
    Medical Device
    Distribution
    Distributed nationwide