The Recall Desk

State

Hawaii product recalls

72,966 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 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4401–4425 of 75733

  • HighFDA (Devices)·Z-0501-2026·2025-11-19

    Positive control serum recalled over negative recovery of the HBsAg analyte

    Techno-Path is recalling 76 units of Multichem ID-B positive control serum because of potential negative recovery of the HBsAg analyte on the Alinity i platform.

    Product
    Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an unassayed positive qualitative quality control serum to monitor the precision of laboratory testing procedures for the determination of anti-HIV-1 IgG, anti-HBc IgG, anti-HTLV-I IgG, anti-HCV IgG, HBs antigen
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Devices)·Z-0493-2026·2025-11-19

    Food allergen panels recalled over barcodes causing wrong tube scanning order

    Siemens Healthcare Diagnostics is recalling 28 units of Food Panel 3 Specific Allergen because barcode orientation causes the instrument to misread tube positions in the holder wedge.

    Product
    Food Panel 3 Specific Allergen; Siemens Material Number (SMN): 10385891; Catalog Number: FP3L4;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0452-2026·2025-11-19

    Lithotripsy transducers recalled over startup failures and handpiece temperature rise

    Olympus is recalling 1,528 ShockPulse Lithotripsy Transducers because the device may fail to start or stop shortly after starting, and the handpiece body may heat up during clinical use.

    Product
    Brand Name: Lithotriptor, Ultrasonic Product Name: ShockPulse Lithotripsy Transducer Model/Catalog Number: SPL-T Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse tra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0477-2026·2025-11-19

    Maryland jaw sealers 44 cm recalled over trapped residual material

    Medline is recalling 9,547 reprocessed LigaSure Maryland Jaw sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0182-2026·2025-11-19

    Dietary supplement recalled because it contains magnesium salicylate

    Professional Botanicals is recalling 430 bottles of Total Comfort capsules because the product contains magnesium salicylate.

    Product
    Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 60, Dose: 2 Capsules. Product Sku: PB173.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0181-2026·2025-11-19

    Nutra Calm supplement recalled because it contains magnesium salicylate

    Professional Botanicals is recalling 452 bottles of Nutra Calm capsules because the product contains magnesium salicylate.

    Product
    Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 90, Dose: 2 Capsules. Product Sku: PB248
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0481-2026·2025-11-19

    Oxygen concentrator batteries recalled over a chip that can stop oxygen

    Philips Respironics is recalling 56 SimplyGo Mini standard battery kits because a defective chip can make the battery fail, shutting down the concentrator and stopping oxygen delivery.

    Product
    SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: SimplyGo Mini Portable Oxygen Concentrator Product code: 1113600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0456-2026·2025-11-19

    Portrait vital signs monitors recalled over batteries losing backup power

    GE Healthcare is recalling 5,990 Portrait VSM patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.

    Product
    Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0500-2026·2025-11-19

    Platelet reactivity tests recalled after an uncleared device was distributed

    Accriva Diagnostics is recalling 125 boxes, 3,125 tests, of VerifyNow PRUTest because a device without premarket clearance was incorrectly packaged and distributed.

    Product
    VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood test used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0466-2026·2025-11-19

    Radiography systems recalled over ceiling carriages that are hard to move

    Philips is recalling 284 Radiography 7300 C systems because some ceiling suspension telescopic carriages may be difficult to move vertically.

    Product
    Radiography 7300 C; Model Number: 712037;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0464-2026·2025-11-19

    DigitalDiagnost 4 systems recalled over ceiling carriages hard to move

    Philips is recalling 12 DigitalDiagnost 4 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.

    Product
    DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0465-2026·2025-11-19

    DigitalDiagnost C90 systems recalled over ceiling carriages resisting vertical movement

    Philips is recalling 223 DigitalDiagnost C90 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.

    Product
    DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0484-2026·2025-11-19

    Laboratory cuvette arrays recalled over barcodes the analyser cannot read

    Becton Dickinson is recalling 29,760 BD Kiestra Isolate Suspension Cuvette Arrays because formatting errors in the 2D barcodes stop the analyser reading the expiration date.

    Product
    BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0479-2026·2025-11-19

    ACL restoration implants recalled from one lot held in sales stock

    Miach Orthopaedics is recalling 167 BEAR Implants from a single lot, in an action the record says was limited to sales force trunk stock.

    Product
    BEAR Implant (Bridge-Enhanced ACL Restoration); Model/Catalog: 1000;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E077000·2025-11-18

    Volvo Trucks Recalls Bendix EC80 Electronic Control Units for Software Defect

    Volvo Trucks is recalling certain Bendix EC80 Advanced Electronic Control Units due to a software defect that may cause safety systems to fail, increasing crash risk.

    Product
    SERVICE BRAKES, AIR:ANTILOCK:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E078000·2025-11-18

    Mack Trucks Recalls Certain Vehicles Due to Electronic Control Unit Defect

    Mack Trucks is recalling certain vehicles because electrical noise may cause the electronic control unit to malfunction, potentially disabling safety systems like ABS and increasing crash risk.

    Product
    SERVICE BRAKES, AIR:ANTILOCK:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V798000·2025-11-18

    2024 Kawasaki Ninja ZX-6R Motorcycles Engine Stall Recall

    Kawasaki is recalling 2024–2026 Ninja ZX-6R motorcycles because a metal crankshaft bushing may seize, causing engine stall and increasing crash risk. Owners are advised not to ride until dealers re-tighten the bushing free of charge.

    Product
    KAWASAKI — KAWASAKI NINJA ZX-6R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V797000·2025-11-17

    Hyundai IONIQ 5 front seat belt retractors may not be secured

    Hyundai is recalling certain 2025 IONIQ 5 vehicles because the seat belt retractors for the driver and front passenger seats may not be securely fastened.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V791000·2025-11-17

    Thor motorhome solar panel mounting brackets can loosen or break

    Thor Motor Coach is recalling certain 2022-2024 Tellaro, Sequence, Twist, Dazzle and other RVs because the solar panel mounting brackets may loosen or break, allowing the panel to detach.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TWIST, TRANQUILITY, DAZZLE, FREEDOM ELITE VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V792000·2025-11-17

    Thor motorhome solar panel adhesive can fail allowing detachment

    Thor Motor Coach is recalling certain 2022-2024 Tellaro, Sequence, Dazzle, Scope, Rize and Twist RVs because the adhesive securing the solar panels to the roof may fail.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TELLARO, RIZE, DAZZLE, SEQUENCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V795000·2025-11-17

    Peterbilt 567 and 589 Trucks Recalled for Brake Air Tank Defect

    PACCAR is recalling 2026 Peterbilt 567 and 589 trucks because air tanks have insufficient volume, potentially reducing braking performance.

    Product
    PETERBILT — PETERBILT 589, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V796000·2025-11-17

    Hyundai Sonata fuel tank can expand and melt against hot exhaust

    Hyundai is recalling certain 2020-2023 Sonata vehicles because a damaged check valve can let air into the fuel tank, causing it to expand, contact hot exhaust components and melt.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide