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.

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.

39351–39375 of 82345

  • SevereNHTSA·19V026000·2019-01-07

    Keystone Recalls Dutchmen Travel Trailers Due to Tire Clearance Issue

    Keystone RV is recalling 2017-2019 Dutchmen Voltage and 2019 Endurance travel trailers because tires may contact the rear floor support, affecting handling.

    Product
    DUTCHMEN — DUTCHMEN VOLTAGE, ENDURANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V001000·2019-01-07

    Ford Recalls Vehicles for Air Bag Inflator Explosion Risk

    Ford is recalling specific 2010-2014 models because passenger air bag inflators may explode due to humidity, posing a serious injury risk.

    Product
    FORD — FORD, LINCOLN, MERCURY MUSTANG, RANGER, EDGE, MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E004000·2019-01-06

    WSB SC101 Motorcycle Helmets Recalled for Impact Protection Failure

    WSB Inc is recalling SC101 half-helmets manufactured in January 2018 because they may not adequately protect the wearer's head during an impact.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V025000·2019-01-04

    Vantage AMS Edge II Recalled for Fuel Leak Fire Risk

    Vantage Mobility International is recalling 2014-2017 AMS Edge II vehicles because a deteriorating fuel pump gasket may cause fuel leaks, increasing fire risk.

    Product
    VANTAGE — VANTAGE AMS EDGE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0820-2019·2019-01-02

    Apio Recalls Eat Smart Salad Shake Ups Due to Listeria

    Apio, Inc. is recalling specific varieties of Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes.

    Product
    Eat Smart Salad Shake Ups - Raspberry Acai/Framboises ET: 5.5 oz. (156 g); US UPC 7 09351-30178 0; Canadian UPC: 7 09351 30196 4. Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
    Category
    Food
    Distribution
    14 states
  • CriticalNHTSA·19E003000·2019-01-02

    Takata Frontal Passenger Air Bag Inflator Recall for 2010+ Vehicles

    Takata is recalling specific frontal passenger air bag inflators in 2010 or newer vehicles registered in 22 states due to a risk of explosion.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0821-2019·2019-01-02

    Apio Recalls Eat Smart Salad Shake Ups Due to Listeria

    Apio, Inc. is recalling Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes in the product.

    Product
    Eat Smart Salad Shake Ups - Sweet Kale/Chou Frise Doux: 5.5 oz. (156 g); US UPC 7 09351-30240 4; Canadian UPC: 7 09351 30243 5. Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-0819-2019·2019-01-02

    Apio Recalls Eat Smart Salad Shake Ups Due to Listeria Risk

    Apio, Inc. is recalling Eat Smart Salad Shake Ups in Avocado Ranch flavor because the Canadian Food Inspection Agency detected Listeria monocytogenes in the product.

    Product
    Eat Smart Salad Shake Ups - Avocado Ranch/Ranch et Avocats: 5.5 oz. (156 g); US UPC: 7 09351-30177 3; Canadian UPC: 7 09351 30195 7; Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-0818-2019·2019-01-02

    Apio Recalls Eat Smart Salad Shake Ups Due to Listeria

    Apio, Inc. is recalling specific varieties of Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes.

    Product
    Eat Smart Salad Shake Ups - Asian Sesame/Sesame Asiatique; 5.5 oz. (156 g); UPC 7 09351-30241 1, 7 09351 30244 2 Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Food)·F-0752-2019·2019-01-02

    Moonstruck Sea Salt Caramels Recalled for Undeclared Hazelnut Allergen

    Moonstruck Chocolate Company is recalling Sea Salt Caramels Tumbled in Milk Chocolate because the product may contain undeclared hazelnuts.

    Product
    Sea Salt Caramels Tumbled In Milk Chocolate, Moonstruck brand. The product sold in an individual resealable plastic bag, net wt. 4 oz. The product is number is 312235 and the UPC code is 7 11175 12235 9. The product also sold in cardboard box of 8/4 oz. bags. The box…
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0822-2019·2019-01-02

    Apio Recalls Eat Smart Salad Shake Ups Due to Listeria Risk

    Apio, Inc. is recalling Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes in the product.

    Product
    Eat Smart Salad Shake Ups - Tropical Lime/Lime Tropicale 5.5 oz. (156 g); US UPC 7 09351-30179 7; 7 09351 30197 1 Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-0681-2019·2019-01-02

    Medical Action Industries Recalls Laparotomy Sponges Due to Sterility Compromise

    Medical Action Industries is recalling 2,600 laparotomy sponges because a breach of the sterile barrier may have compromised product sterility.

    Product
    Laparotomy Sponge, XR No Loop, Single-Use, Sterile, 18'' x 18'' pre-washed with bands without handles, 5 sponges/pack, 40 packs/case. X-Ray Detectable, 1 Non-Absorbent outer wrap. intended use: Laparotomy sponges are intended for use inside the body, surgical incision, or for…
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Food)·F-0755-2019·2019-01-02

    Sargento Recalls Frozen Unbreaded Cheese Products for Listeria and Salmonella Risk

    Sargento Foods is recalling specific frozen unbreaded cheese products due to potential contamination with Listeria monocytogenes or Salmonella.

    Product
    Frozen Unbreaded French onion / Swiss and Onion CC. Sample Number 17-0160.01. Keep Frozen at 0-degrees or below zero. "Food for Research or Evaluation Use". Sargento Technical Center, Elkhart Lake, WI 53020
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·19V022000·2019-01-02

    Pierce Aerial Vehicles Recalled for Unexpected Ladder Rotation Defect

    Pierce Manufacturing is recalling 2004-2018 aerial vehicles because the aerial device may unexpectedly rotate right during extension, increasing injury risk.

    Product
    PIERCE — PIERCE ENFORCER, DASH, QUANTUM, VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0683-2019·2019-01-02

    Medtronic MiniMed Insulin Pumps Recalled for Missing Audio Alerts

    Medtronic is recalling specific MiniMed insulin pump models because software version 4.10 may fail to play expected audio sounds during alerts, alarms, or sirens.

    Product
    Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G (International)
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-0674-2019·2019-01-02

    Tosoh Bioscience Recalls ST AIA-PACK Testosterone Diagnostic Test Kits

    Tosoh Bioscience is voluntarily recalling ST AIA-PACK Testosterone kits due to a Class II defect. The recall covers 26,745 units distributed nationwide.

    Product
    ST AIA-PACK Testosterone (TES) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers. Measurement of testosterone is used to aid in the diagnosis and management of conditions involving…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0753-2019·2019-01-02

    Sargento Recalls Frozen Unbreaded Egg and French Onion Samples for Contamination

    Sargento Foods is recalling specific frozen unbreaded egg and French onion samples due to potential Listeria monocytogenes or Salmonella contamination.

    Product
    Frozen Unbreaded Egg, 3 Cheese and caramelized onion. Sample Number 18-0115.01. Keep Frozen at 0-degrees or below zero. "Food for Research or Evaluation Use". Sargento Technical Center, Elkhart Lake, WI 53020
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0663-2019·2019-01-02

    ICU Medical Recalls Iced Thermoset Closed-Loop Injectate Delivery Systems

    ICU Medical is recalling Iced Thermoset Closed-Loop Injectate Delivery Systems due to a defect in the thermoset check valve that may cause leakage.

    Product
    Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1 unit per Cavity #2-4"x9" Cav/20 pieces per case R1-15645
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Food)·F-0754-2019·2019-01-02

    Sargento Recalls Frozen Unbreaded Egg and Cheese Products for Listeria Risk

    Sargento Foods is recalling specific frozen unbreaded egg and cheese products due to potential Listeria monocytogenes or Salmonella contamination.

    Product
    Frozen Unbreaded Egg, Gouda, caramelized onion. Sample Number 18-0116.01. Keep Frozen at 0-degrees or below zero. "Food for Research or Evaluation Use". Sargento Technical Center, Elkhart Lake, WI 53020
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0661-2019·2019-01-02

    ICU Medical Recalls Thermoset Room Temperature Injectate Delivery Systems

    ICU Medical is recalling 27,250 Thermoset Room Temperature Closed Loop Injectate Delivery Systems due to a defect in the thermoset check valve component that may cause leakage.

    Product
    Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit per Cavity #3 Cavity Deep/20 pieces per case R1-6090
    Category
    Medical Device
    Distribution
    31 states