The Recall Desk

State

Washington product recalls

72,919 recalls have nationwide distribution and so reach Washington. 8,456 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,456
Critical
867
Severe
2,006
Most recent
2026-09-09

Of the 8,456 recalls naming Washington we have scored against our rubric, 867 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,006 (24%) are Severe.

These figures cover only the 8,456 recalls whose distribution notice names Washington specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1901–1925 of 81375

  • ModerateFDA (Devices)·Z-2150-2026·2026-05-20

    Revolution CT X-ray Computed Tomography System Security Vulnerability Recall

    GE HealthCare is recalling Revolution CT x-ray computed tomography systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription. The vulnerability affects certain Revolution Apex, Revolution Ascend, and Revolution CT systems worldwide.

    Product
    Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2195-2026·2026-05-20

    Daig Livewire Steerable Electrophysiology Catheter Incomplete Seals Recall

    Stryker Sustainability Solutions is recalling 206 units of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on sterile product. The catheters were distributed nationwide and in Israel and Canada.

    Product
    Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2172-2026·2026-05-20

    Edwards EVOQUE Tricuspid Delivery System Labeling Update for Valve Functionality

    Edwards Lifesciences is updating labeling for the Edwards EVOQUE tricuspid delivery system (REF 9850TDS) to provide a warning if valve replacement delivery system functionality becomes compromised.

    Product
    Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2135-2026·2026-05-20

    DonJoy IceMan CLASSIC3 Cold Therapy Unit Connector Defect

    DJO, LLC is recalling the DONJOY IceMan CLASSIC3 cold therapy unit (Model 11-1422) due to a broken connector that may interrupt prescribed cold therapy treatment.

    Product
    Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,RH Model/Catalog Number: 11-1422 Software Version: no Product Description: 11-1422 - ICEMAN W/,UNIV,LOOP,NS,RH The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2168-2026·2026-05-20

    Hologic 3DIMENSIONS MAMMOGRAPHY SYSTEM medical device recall

    Hologic is recalling certain 3DIMENSIONS MAMMOGRAPHY SYSTEM models due to internal bolts that may become loose, missing, or broken over time. The FDA classified this as a Class II recall.

    Product
    3DIMENSIONS MAMMOGRAPHY SYSTEM; Model Numbers: 3DM-SYS-INTL2D, 3DM-SYS-INTL2D-MOB, 3DM-SYS-INTL2D-NS, 3DM-SYS-INTL3D, 3DM-SYS-INTL3D-MOB, 3DM-SYS-INTL3D-NS, 3DM-SYS-STD, 3DM-SYS-STD-MOB, 3DM-SYS-STD-NS.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2161-2026·2026-05-20

    LUCAS Chest Compression Systems Recalled for Inadequate Service Documentation

    Jolife AB is recalling 153 LUCAS chest compression systems (Models 2, 3, and 3.1) due to incomplete service documentation. Service work performed on affected systems was not properly documented in service records.

    Product
    LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog Number: 99576-000043 UDI-DI code: 00883873861875 LUCAS 3.1 Model Number: 99576 Catalog Number: 99576-000063 UDI-DI code: 0088
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2170-2026·2026-05-20

    Philips Azurion X-Ray System Cable Hose Carriers May Loosen or Break

    Bolts and plastic parts of cable hose carriers on Philips Azurion X-ray systems may loosen or break during monitor movement or rotation, potentially causing the cable hose to become unsecured.

    Product
    Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222, 722230), Azurion 5 (722281), Azurion 5 M12 (722227, 722231), Azurion 5 M20 (722228, 722232, 722281), Azurion 7 (722282), Azurion 7 B12 (722225, 722235), Azurion 7 B20 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2149-2026·2026-05-20

    Revolution Ascend CT scanner security vulnerability affecting AW Server

    GE HealthCare is recalling Revolution Ascend computed tomography systems due to a potential security vulnerability in the AW Server used with Edison Health Link-based CT Smart Subscription. 25 units are affected nationwide.

    Product
    Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2154-2026·2026-05-20

    Revolution Apex X-ray CT System Security Vulnerability Recall

    GE HealthCare is recalling Revolution Apex, Revolution Ascend, and Revolution CT systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link-based CT Smart Subscription. The vulnerability may impact system security.

    Product
    Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0527-2026·2026-05-20

    Buprenorphine Hydrochloride Injection Recall Due to Particulate Matter

    Endo USA, Inc. is recalling Buprenorphine Hydrochloride injection vials distributed nationwide due to the presence of particulate matter identified as Buprenorphine free base. The FDA classified this as a Class II recall.

    Product
    BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V314000·2026-05-18

    Hyundai Ioniq rear suspension fasteners may loosen and detach

    Hyundai is recalling certain 2025 Ioniq 5 and 2026 Ioniq 9 vehicles because the rear suspension fasteners may loosen and detach, which can cause a loss of vehicle control.

    Product
    HYUNDAI — HYUNDAI IONIQ 9, IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V313000·2026-05-18

    2026 Keystone Alpine recreational trailers recalled for loose shock bolts

    Keystone RV Company is recalling certain 2024–2026 recreational trailers because shock bolts may have been incorrectly tightened, which could cause loss of vehicle stability and increase crash risk.

    Product
    KEYSTONE — KEYSTONE ALPINE, WALKABOUT, MONTANA, COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V316000·2026-05-18

    2025–2026 Hyundai Tucson and Santa Cruz Front Camera Software Issue

    Hyundai is recalling certain 2025 and 2026 Tucson, Tucson Hybrid, Tucson PHEV, and Santa Cruz vehicles due to front camera software that may cause the forward collision avoidance system to activate prematurely and unexpectedly apply the brakes, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI TUCSON, TUCSON PLUG-IN HYBRID, SANTA CRUZ, TUCSON HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V315000·2026-05-18

    Tesla 2025-2026 Model Y Vehicles Missing Certification Label

    Tesla is recalling certain 2025 and 2026 Model Y vehicles because the certification label may not have been installed. Missing weight information on the label could lead to vehicle overloading and increase crash risk.

    Product
    TESLA — TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V310000·2026-05-15

    Altec Recalls Aerial Devices Due to Emergency Stop Failure

    Altec is recalling specific aerial device vehicles because the ground-level emergency stop may fail to halt hydraulic functions in ePTO mode, increasing injury risk.

    Product
    ALTEC — ALTEC AM SERIES AERIAL DEVICE, AA SERIES AERIAL DEVICE, LR SERIES AERIAL DEVICE, AT SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V307000·2026-05-14

    Hyundai Recalls Elantra Vehicles Due to Air Bag Inflator Rupture Risk

    Hyundai is recalling 2015-2016 Elantra and 2016 Elantra GT vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of injury from metal fragments.

    Product
    HYUNDAI — HYUNDAI ELANTRA GT, ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26490·2026-05-14

    Guidecraft Kitchen Helper Towers Recalled Due to Fall Hazard Risk

    Guidecraft Kitchen Helper Towers are being recalled because the internal platform can loosen, become unstable, or detach, creating a fall hazard for young children. The company has received 11 reports of falls, including three injuries.

    Product
    Guidecraft Kitchen Helper Towers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26483·2026-05-14

    Misco Sports Badminton Toy Sets Recalled Due to Battery Ingestion Risk

    Missry Associates is recalling Misco Sports Badminton Toy Sets because the shuttlecocks contain button cell batteries that children can easily access and swallow, potentially causing serious internal injuries or death.

    Product
    Misco Sports Badminton Toy Sets Red/Blue MT2383
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26485·2026-05-14

    Agio Menlo Woven Patio Swings Recalled Due to Fall Hazard Risk

    World Bright International Limited recalls Agio Menlo Woven Patio Swings (Model 1934256) sold at Costco because the swing seat can detach during use, risking serious injury or death. Eight injuries have been reported.

    Product
    Agio Menlo Woven Patio Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26481·2026-05-14

    Tiyol Pull String Teething Toys Recalled for Choking Hazard Risk

    Tiyol Pull String Teething Toys sold on Amazon are recalled due to oversized silicone strings that can lodge in the throat, posing a choking hazard. CPSC is aware of 11 choking incidents.

    Product
    Tiyol Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26494·2026-05-14

    Electric Start Pressure Washers Recalled for Carbon Monoxide Hazard

    Generac and DR Power electric start pressure washers are recalled because the electronic start/stop button can malfunction and self-start the unit, creating a risk of serious injury or death from carbon monoxide poisoning in confined spaces. No injuries have been reported.

    Product
    Electric Start Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26493·2026-05-14

    Cosyland Children's Tower Stools Recalled for Entrapment and Fall Hazards

    Cosyland Children's Tower Stools can collapse, tip over, or trap a child's torso through front and back openings, posing risks of serious injury and death. The firm is aware of 25 reports of stability issues and falls, with eight injuries including a fractured arm.

    Product
    Cosyland Children's Tower Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide