The Recall Desk

State

Washington product recalls

73,809 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,536
Critical
865
Severe
2,405
Most recent
2026-11-04

Of the 8,536 recalls naming Washington we have scored against our rubric, 865 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,405 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,536 recalls whose distribution notice names Washington specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40701–40725 of 82345

  • LowFDA (Devices)·Z-0075-2019·2018-10-10

    Smiths Medical Portex Nasal Oxygen Cannula Recalled for Labeling Error

    Smiths Medical ASD Inc. is recalling 850 Portex First Breath Nasal Oxygen Cannulas because the 'Manufactured' and 'Use By' dates are transposed, incorrectly suggesting the product expired before it was made.

    Product
    smiths medical portex First Breath Nasal Oxygen Cannula, REF 001293, with Gas Monitoring Line, 305 cm (10ft.) & Female Luer Connector, 213 cm (7ft.) Tubing, & Oxygen Adapter. Product Usage: For the administration of nasal oxygen and humidity to patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0018-2019·2018-10-10

    Otsuka Recalls Mislabeled Abilify and Abilify Maintena Physician Sample Kits

    Otsuka is recalling 4,738 physician sample kits of Abilify and Abilify Maintena due to labeling errors, including misspelled product names and missing storage instructions.

    Product
    treatNOW ABILIFY (aripiprazole) / ABILIFY MAINTENA 400-mg (aripiprazole) for extended release injectable suspension. Kit contents 2 packs Abilify Tablets 10 mg (14 day supply) plus 1 Abilfy Maintena Vial Kit.Rx only. Distributed and Marketed by: Otsuka America Pharmaceutical…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0062-2019·2018-10-10

    Dannoritzer Laparoscopy Instruments IFU Recalled for Unvalidated Cleaning Instructions

    Dannoritzer Medizintechnik GmbH & Co. KG is recalling Instructions For Use (IFU) for certain laparoscopy instruments because the manual cleaning process was not validated.

    Product
    Laparoscopy Instruments Instructions For Use (IFU) for the following: 1)Monopolar electrode, 2) Insert, handle and/or shaft component of a modular forceps or scissors for electrosurgical coagulation, 3) One-piece forceps or scissors for electrosurgical coagulation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0072-2019·2018-10-10

    Smiths Medical Nasal Cannula Recalled for Incorrect Labeling

    Smiths Medical ASD Inc. is recalling 2,550 adult nasal cannulas because the 'Manufactured' and 'Use By' labels are transposed, suggesting the product expired before it was manufactured.

    Product
    smiths medical portex First Breath Adult Nasal Cannula, REF 001285, Flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0073-2019·2018-10-10

    Smiths Medical Portex Nasal Cannula Recalled for Labeling Error

    Smiths Medical ASD Inc. is recalling 3,000 Portex First Breath Adult Nasal Cannulas because the 'Manufactured' and 'Use By' labels are transposed, suggesting the product expires before it was manufactured.

    Product
    smiths medical portex First Breath Adult Nasal Cannula, REF 001289, Curved Flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0071-2019·2018-10-10

    Smiths Medical Nasal Cannula Recalled for Transposed Date Labels

    Smiths Medical ASD Inc. is recalling 12,000 First Breath Adult Nasal Cannulas because the 'Manufactured' and 'Use By' labels are transposed, incorrectly suggesting the product expired before it was manufactured.

    Product
    smiths medical portex First Breath Adult Nasal Cannula, REF 001283, Non-flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V708000·2018-10-09

    Altec Recalls 2014-2018 Cranes Due to Incorrect Load Chart Display

    Altec is recalling 2014-2018 AC40-152S cranes because the electronic load protection screen may display incorrect values, risking unit instability or loss of load control.

    Product
    ALTEC — ALTEC CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V706000·2018-10-09

    Altec Recalls Aerial Devices and Digger Derricks Due to Step Defect

    Altec is recalling 2017-2018 aerial devices and digger derricks because a step on the fiberglass platform can break off, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V705000·2018-10-09

    Thor Motor Coach Recalls 2013 Motorhomes Due to Wiper Defect

    Thor Motor Coach is recalling 2,854 specific 2013 motorhome models because incorrectly installed windshield wipers may fail, reducing driver visibility and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ACE, PALAZZO, WINDSPORT, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19006·2018-10-09

    Marker Recalls Kingpin Ski Bindings Due to Fall Hazard

    Marker is recalling Kingpin 10 and 13 ski bindings because steel pins can break, reducing release force and causing a fall hazard. No injuries have been reported.

    Product
    Kingpin 10 and Kingpin 13 alpine touring ski bindings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V703000·2018-10-05

    Daimler Trucks Recalls 2018-2019 Models for Loose Brake Caliper Bolts

    Daimler Trucks North America is recalling 2018-2019 Freightliner, Western Star, and FCCC trucks because brake caliper mounting bolts may be insufficiently tightened, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC, WESTERN STAR 114SD, XBS, XCM, XCP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V704000·2018-10-05

    Hyundai Recalls Ioniq Hybrids for Potential Fire Risk

    Hyundai is recalling 2017-2018 Ioniq Hybrid and 2018 Plug-In Hybrid vehicles because a faulty relay may overheat the rear seat, increasing the risk of a fire.

    Product
    HYUNDAI — HYUNDAI IONIQ HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V702000·2018-10-05

    Thomas Built Buses Recalls 2018-2019 Models Due to Brake Caliper Bolts

    Daimler Trucks North America is recalling 2018-2019 Thomas Built school buses because brake caliper mounting bolts may be insufficiently tightened, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V698000·2018-10-05

    Thomas Built Buses Minotour Recalled for Rear Emergency Exit Door Defect

    Daimler Trucks North America is recalling 2016-2019 Thomas Built Buses Minotour school buses because the rear emergency exit door may not open wide enough to meet federal safety standards.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E094000·2018-10-05

    Truck-Lite Recalls Right-Hand Headlights for International LT Trucks

    Truck-Lite is recalling right-hand headlights for 2016-2019 International LT trucks due to incorrect markings that may lead to improper aiming and reduced visibility.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·085-2018·2018-10-04

    JBS Tolleson Recalls Raw Beef Products Due to Salmonella Newport Contamination

    JBS Tolleson is recalling approximately 6.9 million pounds of raw beef products potentially contaminated with Salmonella Newport. The recall follows an investigation linking the bacteria to 57 reported illnesses.

    Product
    JBS Tolleson Inc. — JBS Tolleson, Inc. Recalls Raw Beef Products Due to Possible Salmonella Newport Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V685000·2018-10-04

    Toyota Recalls 2018-2019 Models for Air Bag Software Defect

    Toyota is recalling specific 2018-2019 Avalon, Sequoia, Tundra, and Avalon Hybrid vehicles because the air bag software may prevent deployment in a crash.

    Product
    TOYOTA — TOYOTA AVALON, SEQUOIA, TUNDRA, AVALON HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V694000·2018-10-04

    Suzuki Recalls 2017-2018 Motorcycles for Fuel Pump O-Ring Defect

    Suzuki is recalling 2017-2018 DL650, GSX-R1000, and GSX-S750 motorcycles because a twisted fuel pump O-ring may cause a fuel leak, increasing fire risk.

    Product
    SUZUKI — SUZUKI DL650, GSX-R1000, GSX-S750
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V684000·2018-10-04

    Toyota Recalls Prius and Prius V for Hybrid System Shutdown Risk

    Toyota is recalling 2010-2014 Prius and 2012-2014 Prius V vehicles because excessive voltage may cause the hybrid system to shut down, increasing crash risk.

    Product
    TOYOTA — TOYOTA PRIUS, PRIUS V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V693000·2018-10-04

    Altec Recalls 2017 Aerial Devices Due to Electrical Shock Risk

    Altec is recalling 2017 AT37, AT41, and AT48 aerial devices because an incorrectly installed hose sock may cause electrical shock.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide