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.

39701–39725 of 82345

  • SevereNHTSA·18V843000·2018-11-28

    Keystone RV Recalls 2019 Travel Trailers Due to Axle Hub Bearing Defect

    Keystone RV Company is recalling certain 2019 recreational trailers because the inner axle hub bearings may not have been sufficiently greased, which could cause overheating, hub failure, and increased crash risk.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN OUTBACK, BULLET, AEROLITE, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V846000·2018-11-28

    Blue Bird Recalls School Buses Due to Seat Detachment Risk

    Blue Bird is recalling certain 2019-2020 school buses because seats may detach from the floor in a crash, increasing injury risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0268-2019·2018-11-28

    Sciegen Pharmaceuticals Recalls Irbesartan Tablets Due to NDEA Impurity

    Sciegen Pharmaceuticals is recalling Irbesartan Tablets, 150 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).

    Product
    Westminister Irbesartan Tablets, USP, 150 mg, (a) 30-count bottle (NDC 69367-120-01), (b) 90-count bottle (NDC 69367-120-03), Rx Only, Manufactured by ScieGen Pharmaceuticals Inc. Hauppauge, NY 11755, Manufactured for Westminster Pharmaceuticals LLC Olive Branch, MS 20854, Made…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0474-2019·2018-11-28

    Boston Scientific Recalls SQ-RX Pulse Generators for Battery Malfunctions

    Boston Scientific is recalling 12,900 SQ-RX Pulse Generators used in S-ICD systems due to latent internal battery malfunctions that cause accelerated depletion.

    Product
    The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The S-ICD System is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V848000·2018-11-28

    Honda Recalls 2019 Ridgeline and Pilot for Air Bag Deployment Risk

    Honda is recalling 2019 Ridgeline and Pilot vehicles because a trim panel clip may interfere with right-side curtain air bag deployment in a crash.

    Product
    HONDA — HONDA RIDGELINE, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0656-2019·2018-11-28

    Path of Life Southwest Quinoa Recalled for Listeria and Salmonella Risk

    Harvest Food Group is recalling Path of Life All Natural Southwest Quinoa due to potential contamination with Listeria monocytogenes or Salmonella.

    Product
    Path of Life All Natural Southwest Quinoa; 10oz., 6 and 12 units per case; Keep Frozen; UPC 855229005035; Item# POL-RSWN-1210 and POL-RSWQ-0610
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-0475-2019·2018-11-28

    Tosoh AIA-2000 Analyzer Recall Due to Potential Wash Solution Defect

    Tosoh Bioscience is recalling seven AIA-2000 analyzers because a liquid suction pump defect may cause incomplete washing, leading to inaccurate test results.

    Product
    AIA-2000 Analyzer, Model Nos. AIA-2000LA, AIA-2000ST - Product Usage: The AIA-2000 is capable of performing three methods of immunoassay: an immunoenzymetric (IEMA) or sandwich immunoassay, a competitive binding (EIA) immunoassay, and a two-step immunoenzymetric immunoassay. An…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0623-2019·2018-11-28

    Cadence Gourmet Recalls Roasted Corn Salsa for Potential Contamination

    Cadence Gourmet LLC is recalling Roasted Corn Salsa manufactured for Corner Bakery Café due to potential Salmonella and/or Listeria monocytogenes contamination.

    Product
    Roasted Corn Salsa; Net Weight: 10 lbs. (10 x 1 lb. bags) Corner Bakery Caf¿ Brand Ingredients: Corn, Red Onion, Jalapeno, Lime Juice, Canola Oil, Cilantro, Salt. Keep Frozen. Manufactured for Corner Bakery Caf¿, Cornet Bakery Caf¿, Callas, TZ 75251
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0626-2019·2018-11-28

    Cadence Gourmet Cauliflower & Cheese recall due to potential Salmonella and Listeria contamination

    The FDA is recalling Cadence Gourmet Cauliflower & Cheese because of potential Salmonella and/or Listeria Monocytogenes contamination.

    Product
    Cadence Gourmet Cauliflower & Cheese Net Weight: 10 lbs. (4.4 kg) / cs UPC: 00851124006375 Ingredients: Cauliflower, B¿chamel Sauce (Milk, Cultured Cream, Vegetable Broth [Water, sauteed Vegetables {carrots, celery, onions, tomatoes}, Salt, Yeast Extract, Dried Onion and…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0482-2019·2018-11-28

    GE Healthcare Recalls Panda iRes Infant Radiant Warmers Due to Electric Leakage

    GE Healthcare is recalling 1,724 Panda iRes Infant Radiant Warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Panda iRes Infant Radiant Warmer. Device sold under the following product names: Panda iRes Warmer and Panda iRes Bedded Warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0624-2019·2018-11-28

    Cadence Gourmet Roasted Vegetables Recalled for Potential Pathogen Contamination

    Cadence Gourmet LLC is recalling Balsamic Roasted Vegetables due to potential Salmonella and Listeria contamination from McCain Foods USA ingredients.

    Product
    Cadence Gourmet Balsamic Roasted Vegetables; Net Weight: 10 lbs. (4.5 kg)/ cs UPC: 00851124006382 Ingredients: Zucchini, Artichoke, White Balsamic Sauce (Balsamic vinegar {wine vinegar, grape concentrate, Natural Flavor, Contains Sulfites] Olive Oil, Walnut Oil, Honey…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0483-2019·2018-11-28

    GE Healthcare Recalls Panda Freestanding Infant Warmers Due to Electric Leakage

    GE Healthcare is recalling 1,724 Panda Freestanding Infant Warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Panda Freestanding Warmer. Device sold under the following product names: Panda Freestanding Warmer and Panda Freestanding Warmer Generic ATO Model. Infant Radiant warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V844000·2018-11-28

    Porsche Recalls 2017-2018 Models Due to Ski Bag Strap Defect

    Porsche is recalling certain 2017-2018 Cayenne and Macan vehicles because the optional ski bag strap may tear, increasing injury risk in a crash.

    Product
    PORSCHE — PORSCHE CAYENNE, MACAN, MACAN GTS, MACAN S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0266-2019·2018-11-28

    L. Perrigo Recalls Calcium Carbonate Antacid Tablets Due to Metal Particles

    L. Perrigo is recalling specific lots of calcium carbonate antacid tablets because they were found to contain metal particles.

    Product
    Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count bottle, OTC, [Healthy Accents brand NDC: 55316-014-72, Distributed by DZA Brands, LLC, Salisbury, NC 28147, Scarborough, ME 04074], [HealthMart Pharmacy brand NDC: 62011-0295-1, Distributed by McKessen, One…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0481-2019·2018-11-28

    GE Healthcare Recalls Giraffe Infant Warmers Due to Electric Leakage Risk

    GE Healthcare is recalling 1,724 Giraffe infant radiant warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe Warmer. Device sold under the following product names: Giraffe Warmer and Giraffe Bedded Warmer. infant radiant warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0480-2019·2018-11-28

    GE Healthcare Recalls Giraffe Incubator Carestations Due to Electric Leakage

    GE Healthcare is recalling 1,724 Giraffe Incubator Carestations worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe Incubator Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0479-2019·2018-11-28

    GE Healthcare Recalls Giraffe OmniBed Neonatal Incubators Due to Electric Leakage

    GE Healthcare is recalling 1,724 Giraffe OmniBed Carestation neonatal incubators worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe OmniBed Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0625-2019·2018-11-28

    Cadence Gourmet Recalls Roasted Vegetable Blend for Potential Pathogen Contamination

    Cadence Gourmet LLC is recalling Roasted Vegetable Blend due to potential Salmonella and Listeria contamination from McCain Foods USA ingredients.

    Product
    Roasted Vegetable Blend; Net Weight: 30 lbs. (12 x 2.5 lb. bags) Corner Bakery Caf¿ Brand Ingredients: Zucchini, artichoke (water, citric acid and calcium chloride). Tomatoes, olive oil, canola oil, garlic, vinegar (potassium metabisulfite), salt, black pepper, spices.…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0654-2019·2018-11-28

    Harvest Food Group Recalls Mexican Style Roasted Corn for Listeria and Salmonella

    Harvest Food Group is recalling Signature Select Mexican Style Roasted Corn due to potential contamination with Listeria monocytogenes or Salmonella.

    Product
    Signature Select Mexican Style Roasted Corn; 12 oz.; 12/12oz. units per case; Keep Frozen Until Ready To Use; UPC 02113094060; Item# 21130-09406
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-0655-2019·2018-11-28

    Zinetti Roasted Vegetable Blend Recalled for Listeria and Salmonella Risk

    Harvest Food Group is recalling Zinetti Roasted Vegetable Blend due to potential contamination with Listeria monocytogenes or Salmonella.

    Product
    Zinetti Roasted Vegetable Blend; 40lb. bulk case; Keep Frozen; Item# ZIN-RSVB-0040
    Category
    Food
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-0489-2019·2018-11-28

    Merck Minicon Clinical Sample Concentrators Recalled for Performance Issues

    Merck Millipore is recalling Minicon Clinical Sample Concentrators because they may take up to 24 hours to concentrate samples, delaying diagnostic tests.

    Product
    Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon CS-15) Minicon concentrators are non-sterile, disposable, multiwall ultrafiltration devices. Minicon¿ clinical sample concentrators are for in vitro diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0476-2019·2018-11-28

    Ortho-Clinical VITROS dLDL Reagent Recalled for Negatively Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products dLDL Reagent GENs 26 and 27 because the in vitro diagnostic may produce negatively biased results.

    Product
    VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Diagnostic to quantitatively measure LDL Cholesterol (LDLC) Product Code: 6801728 UDI (10758750006793)
    Category
    Medical Device
    Distribution
    Distributed nationwide