The Recall Desk

State

Hawaii product recalls

72,986 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.

Which agencies issued them

These figures cover only the 2,767 recalls whose distribution notice names Hawaii specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6701–6725 of 75753

  • HighFDA (Devices)·Z-1731-2025·2025-05-14

    GALT Centeze Catheter recalled due to potential sterile packaging seal failure

    Galt Medical Corporation is recalling 2,881 GALT Centeze Catheters due to a potential open seal in the sterile barrier packaging. The open seal could compromise sterility of the device.

    Product
    GALT Centeze Catheter REF: DRC-002-05 DRC-002-06 The Centeze is intended for use in percutaneous fluid aspirations and small volume drainage procedures. For both adult and adolescent groups.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1733-2025·2025-05-14

    B Braun Interventional ELITE HV Hemostasis Valve Introducer System Recall

    Galt Medical Corporation is recalling the B Braun Interventional ELITE HV Hemostasis Valve Introducer System (Catalog Number 612802, Model BCL-100-04, Lot S25128171) due to a potential open seal in the sterile barrier packaging. The defect may compromise the sterility of the device.

    Product
    B Braun Interventional ELITE HV Hemostasis Valve Introducer System REF 612802 Model Number: BCL-100-04 The Elite HV¿ Introducer System is indicated for use in percutaneous procedures to introduce catheters and other intravascular devices into the vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1737-2025·2025-05-14

    Introducer Kit-Tearaway MicroSlide Medical Device Recall

    Galt Medical Corporation is recalling Introducer Kit-Tearaway MicroSlide devices used to introduce catheters into blood vessels due to a potential open seal in the sterile barrier packaging. The affected units may not maintain sterility, creating a risk of infection.

    Product
    Introducer Kit- Tearaway MicroSlide REF KIT-051-01, 00841268106130 INT-101-15, 00841268107380 These introducers are used for the procedures to introduce catheters and other intravascular devices into the coronary and peripheral vasculature of adult and pediatric patients of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1728-2025·2025-05-14

    Artix MT Thrombectomy Device recalled for incorrect vessel range specification

    Inari Medical is recalling 45 units of the Artix MT Thrombectomy Device (REF: 32-102, Lot 24100082) because labeling specifies an incorrect vessel range of 2.5-6 mm instead of 3-6 mm, which could increase radial force on arteries and cause vascular complications.

    Product
    Artix MT Thrombectomy Device, REF: 32-102
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1722-2025·2025-05-14

    Philips Microstream Advance Neonatal-Infant CO2 Filter Line Adapter Disconnection Risk

    Philips is recalling Microstream Advance Neonatal-Infant Intubated CO2 Filter Lines and related products because the adapter may be difficult or impossible to disconnect from the endotracheal tube.

    Product
    Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm Lng , Adt/Pedi Intub CO2 Line High Humidity , Adt/Pedi Intub CO2 Line LTerm Lng , Adt/Pedi Intub CO2 Line LTerm , Neo/Inf Intub CO2 Line LTerm ,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V273000·2025-05-14

    Ford Bronco 360-degree cameras may not display a rearview image

    Ford is recalling certain 2022-2023 Bronco vehicles because the 360-degree view camera may not display a rearview image when the vehicle is placed in reverse.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1735-2025·2025-05-14

    Galt Medical Introducer Kit Coaxial Dilator recalled for packaging seal issue

    Galt Medical Corporation is recalling certain Introducer Kit–Coaxial Dilator models due to potential open seals in sterile barrier packaging, which could compromise sterility.

    Product
    Introducer Kit- Coaxial Dilator REF: KIT-002-28, 00841268104730 KIT-002-34, 00841268104792 KIT-002-35, 00841268104808 KIT-011-40, 00841268105553 KIT-011-62, 00841268105614 KIT-038-04, 00841268104556 KIT-039-03, 00841268104587 KIT-039-13, 00841268106055 KIT-081-02 / PS2-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1736-2025·2025-05-14

    Introducer Needle REF NDL-107-04 Sterile Packaging Recall

    Galt Medical Corporation recalls Introducer Needle REF NDL-107-04 due to potential open seals in sterile barrier packaging, which could compromise product sterility.

    Product
    Introducer Needle REF NDL-107-04 These needles are used for the percutaneous introduction of guidewires
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0754-2025·2025-05-14

    Lamb Weston frozen hashbrown patties recalled for plastic contamination

    Lamb Weston Item M7414 frozen hashbrown patties are recalled because approximately 1mm to 8mm pieces of plastic were found in the product. The affected cases were distributed in Arizona, Hawaii, and internationally.

    Product
    Item M7414, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*10044979923820. Made in USA.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0414-2025·2025-05-14

    Testosterone Pellet 200 mg Recalled for Glass Particulate Matter

    BSO LLC is recalling Testosterone Pellet 200 mg vials nationwide due to the presence of glass particles found in pellet vials. Patients should contact their healthcare provider.

    Product
    TESTOSTERONE PELLET 200 mg BLUNT (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0124-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0755-2025·2025-05-14

    Lamb Weston frozen hashbrown patties recalled for plastic contamination

    Lamb Weston Inc is recalling approximately 3,789 cases of frozen hashbrown patties due to the presence of plastic pieces measuring 1–8 mm in the product. No illnesses have been reported.

    Product
    Item M7422, frozen foodservice Lamb Weston Hashbrown Patties LW Formed Oval 6/3.5LB bags per case. GTIN*10044979922687. Made in USA.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1732-2025·2025-05-14

    B Braun Interventional Coaxial Dilator Micro-Introducer Kits Recall

    Galt Medical Corporation is recalling B Braun Interventional Coaxial Dilator Micro-Introducer Kits due to a potential open seal in the sterile barrier packaging. The affected kits are distributed nationwide in eight U.S. states and six countries.

    Product
    B Braun Interventional Coaxial Dilator REF: KIT-018-47, KIT-019-67, KIT-018-41, KIT-019-37 These Micro-Introducer Kits are intended to introduce up to a .038 inch guidewire or catheter into the vascular system following a small gauge needle stick.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1724-2025·2025-05-14

    INSPIRA AIR Balloon Dilation System packaging error corrected nationwide

    Integra LifeSciences is recalling INSPIRA AIR Balloon Dilation System 10x40 cartons because an incorrect product was packaged inside. The recall affects six units distributed across Texas, Montana, Alabama, and Oklahoma.

    Product
    INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0753-2025·2025-05-14

    Lamb Weston Hashbrown Patties recalled for plastic foreign material

    Lamb Weston Inc is recalling frozen foodservice hashbrown patties due to plastic pieces (1–8 mm) found in the product. Affected cases were distributed to Arizona, Hawaii, Japan, Kuwait, Taiwan, and UAE.

    Product
    Item M0053, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN* 50195500004896. Made in USA.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0752-2025·2025-05-14

    Lamb Weston Hashbrown Patties recalled for plastic contamination

    Lamb Weston frozen hashbrown patties may contain pieces of plastic material measuring 1–8 mm. The affected product was distributed in Arizona, Hawaii, and several international locations.

    Product
    Item M7204, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*10044979923813. Made in USA.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1723-2025·2025-05-14

    Ambu aScope 5 Broncho HD Endoscope Labeling Error Recall

    Ambu Inc. is recalling 160 units of the Ambu aScope 5 Broncho HD 5.6/2.8 Sampler Set due to incorrect front pouch labeling that states 5.0/2.2 instead of the correct size 5.6/2.8.

    Product
    Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1721-2025·2025-05-14

    Washer Disinfector Aquadis 56 Model 56M Recalled

    Getinge Disinfection Ab recalls the Washer Disinfector Aquadis 56 (Model 56M) because the frequency inverter is not programmed to specification, causing the circulation pump to start earlier than expected and wear the axial seal prematurely.

    Product
    Washer Disinfector Aquadis 56; Model Number: 56M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1718-2025·2025-05-14

    Bio 1 Granules for Filling implant bone graft material nationwide recall

    Bio 1 Granules for Filling implant bone granules may contain less product than specified on the label. The affected lot is 240781 (UDI: 03760154000369), distributed nationwide.

    Product
    Bio 1 Granules for Filling ¿ 1 mm (2 cm¿), REF:P822692243, Material: BIOSORB (BTCP 95% minimum purity)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1740-2025·2025-05-14

    IntelliSpace Cardiovascular Software Echo Module Data Reporting Issue

    Philips is recalling IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x because the Echo Module may generate reports with missing or incomplete information.

    Product
    IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x; Model Number: 830089.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1734-2025·2025-05-14

    GALT Guidewire SGW-051-07 Sterile Packaging Seal Defect Recall

    Galt Medical Corporation is recalling GALT Guidewire model SGW-051-07 due to a potential open seal in the sterile barrier packaging. The defect may compromise the sterility of the device.

    Product
    GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to introduce and position catheters and other interventional devices within the Coronary and peripheral vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1719-2025·2025-05-14

    Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits Recalled

    One lot of Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits (Model 750830) was stored at improper temperatures in Medline warehouses. The test kits may not perform as intended due to storage outside labeled requirements.

    Product
    Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits, Model Number 750830
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0403-2025·2025-05-14

    Timolol Maleate Ophthalmic Solution Recalled for Defective Container

    FDC Limited is recalling Timolol Maleate Ophthalmic Solution 0.5% due to a defective container where the spike of the cap becomes lodged in the bottle nozzle, preventing users from accessing the solution.

    Product
    TIMOLOL MALEATE — TIMOLOL MALEATE (TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1729-2025·2025-05-14

    Philips Tempus Pro Patient Monitor Software Update for Operational Issues

    Remote Diagnostic Technologies Ltd. is issuing a software update for the Philips Tempus Pro Patient Monitor due to freezing, rebooting, and potential ECG measurement accuracy issues across multiple software versions.

    Product
    Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1738-2025·2025-05-14

    Blueprint Software version 4.2.1 surgical planner access bug

    Tornier's Blueprint Software version 4.2.1 contains a bug that prevents surgeons from accessing surgical cases created in earlier software versions.

    Product
    Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide