The Recall Desk

State

Washington product recalls

73,741 recalls have nationwide distribution and so reach Washington. 8,535 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,535
Critical
865
Severe
2,404
Most recent
2026-10-28

Of the 8,535 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 2,404 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,535 recalls whose distribution notice names Washington specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35526–35550 of 82276

  • HighFDA (Food)·F-2127-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Foreign Plastic Pieces

    Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Chocolate Espresso Item Code CS812079, UPC Code 20053-6, UPC GTIN 10787325200533. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2121-2019·2019-09-18

    Martha White Gluten Free Cornbread Mix Recalled for Gluten Presence

    Hometown Food Company is recalling Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix because the product tested positive for gluten despite being labeled gluten-free.

    Product
    Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix packaged in a 7oz. pouch. 12 pouches per wholesale case. Item UPC: 0 1330082014 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1851-2019·2019-09-18

    Macleods Recalls Pramipexole Dihydrochloride Tablets Due to Subpotency

    Macleods Pharma USA is recalling Pramipexole Dihydrochloride Tablets 0.125 mg because stability studies showed the drug was subpotent.

    Product
    PRAMIPEXOLE DIHYDROCHLORIDE — PRAMIPEXOLE DIHYDROCHLORIDE (PRAMIPEXOLE DIHYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2495-2019·2019-09-18

    Philips 5-Lead ECG Set Recalled Due to Connector Thickness Issue

    Philips is recalling 5-Lead ECG sets because the connector thickness may prevent or impede I 2-Lead ECG measurements.

    Product
    Philips 5-Lead Set, Disposable, Bedside, AAMI Model # 989803173131 Product Usage: Philips Single-Patient-Use ECG lead sets for bedside monitoring are available in 5-lead configuration
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2151-2019·2019-09-18

    FungusAmongUs Shiitake Organic Mushrooms Recalled for Undeclared Sulfites

    Seattle Gourmet Foods Inc. is recalling FungusAmongUs Shiitake Organic Mushrooms due to undeclared sulfites detected by the Florida Department of Agriculture.

    Product
    FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms. Packaged in a clear cellophane bag, net Weight 1 ounce. UPC 7 19870 60023 3 for individual 1 ounce bags UPC 50719870600016 for Master caddy that holds 8 packages of 1 ounce bags The label is read in parts…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2488-2019·2019-09-18

    Philips Recalls Two HeartStart MRx Monitor/Defibrillators for Missing Corrections

    Philips North America, LLC is recalling two HeartStart MRx Monitor/Defibrillators because they may not have received applicable corrections from prior field actions.

    Product
    HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The HeartStart MRx is a lightweight, portable external defibrillator, offering two modes of operation for defibrillation: manual mode and semi-automatic mode (AED). In manual mode, the HeartStart MRx is a full…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2144-2019·2019-09-18

    Calcium Supplement Recalled for Lacking Declared Vitamin D Content

    Jivan Shakti Inc. is recalling 790 bottles of Dr. Naram's Rasayana D Tablet because FDA testing found no Vitamin D in the product.

    Product
    Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C., DR. NARAM'S RASAYANA D TABLET, Calcium Supplement with Vitamin D*, Dietary Supplement, 60 Tablets, FOR EXPORT ONLY, Imported & Distributed by: Jivan Shakti INC, 933 South Street, Peekskill, NY 10566…
    Category
    Food
    Distribution
    20 states
  • LowFDA (Drugs)·D-1848-2019·2019-09-18

    Mylan Recalls Gatifloxacin Ophthalmic Solution Due to Unknown Impurity

    Mylan Pharmaceuticals is recalling Gatifloxacin Ophthalmic Solution 0.5% due to an out-of-specification result for an unknown impurity.

    Product
    Gatifloxacin Ophthalmic Solution 0.5%, 2.5 mL per bottle, Rx Only, Mfd. for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. Made in India. NDC: 0378-5431-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2490-2019·2019-09-18

    Randox Calibration Serum Recalled for Incorrect Analyte Targets

    Randox Laboratories is recalling calibration sera due to realigned targets for AST and ALT. The recall affects 307 kits distributed nationwide and in several foreign locations.

    Product
    This is an in vitro diagnostic product intended for use as a calibration serum in clinical chemistry assays. Randox calibration sera contain 42 analytes and are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1847-2019·2019-09-18

    Lamivudine Tablets Recalled for Incorrect Package Insert Labeling

    American Health Packaging is recalling Lamivudine Tablets due to an error in the package insert that incorrectly lists tablet description coding.

    Product
    Lamivudine Tablets, USP, 150 mg, 30 (3x10) count Unit Dose Blisters Carton, NDC 60687-362-21 (Individual Dose NDC: 60687-362-11), Distributed by American Health Packaging, Columbus, OH
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V656000·2019-09-17

    McNeilus CNG Trucks Recalled for Pressure Relief Device Defect

    McNeilus is recalling 330 CNG-powered trucks from 2013-2018 because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.

    Product
    MCNEILUS — MCNEILUS MA SIDE LOADER, AUTOREACH, STANDARD MIXER, ZERO RADIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V658000·2019-09-17

    Hyundai Translead Recalls 2017-2018 Duralite HT Flatbed Trailers

    Hyundai Translead is recalling 2017-2018 Duralite HT flatbed trailers because bulkhead brackets may break, causing the bulkhead to detach and create a road hazard.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD DURALITE HT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V659000·2019-09-17

    Terex TLM Aerial Vehicles Recalled for Boom Valve Defect

    Terex is recalling 2016-2017 TLM aerial devices because an incorrect holding valve may cause the boom to drift down if a hose bursts.

    Product
    TEREX — TEREX TLM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V655000·2019-09-16

    Airstream Recalls 2016-2017 Trailers Due to Electrical Fire Risk

    Airstream is recalling specific 2016-2017 Flying Cloud and International trailers because an inverter may contact a fuse, creating a fire hazard.

    Product
    AIRSTREAM — AIRSTREAM FLYING CLOUD, INTERNATIONAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V654000·2019-09-12

    Nissan and Infiniti Recall Vehicles for Backup Camera Display Defect

    Nissan is recalling 2018-2019 Nissan and Infiniti vehicles because backup camera settings can be adjusted to hide the rear view image, increasing crash risk.

    Product
    NISSAN — NISSAN, INFINITI ROGUE SPORT, ARMADA, VERSA, ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E062000·2019-09-12

    Chrysler Recalls Mopar Passenger Air Bag Modules Due to Testing Defect

    Chrysler is recalling specific Mopar replacement passenger air bag modules that did not complete developmental testing. These modules may not perform as designed in a crash, increasing injury risk.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2481-2019·2019-09-11

    OMNIlife ApeX Acetabular Liner Recalled for Oxidation Test Failure

    OMNIlife science Inc. is recalling six ApeX acetabular liners that failed oxidation testing. The defect may cause higher wear rates, potentially leading to revision surgery.

    Product
    OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component ApeX-LNK crosslinked Acetabular Insert, 10 deg hood; Product Code : H5-54840
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2098-2019·2019-09-11

    Mountain Mel's Herbal Tea Recalled for Potential Salmonella Contamination

    Mountain Mel's Essential Goods LLC is recalling The Milk Lady's Herbal Tea due to potential Salmonella contamination. The product was distributed in California, Oregon, and Washington.

    Product
    The Milk Lady's Herbal Tea, packaged loose leaf in aluminum tin, net weight 2 oz or 56.5 grams. UPC: 7 99632 05658 4. The label is read in parts: "***The Milk Lady s FOR GREATER MILK FLOW & CALM NERVES***CAFFEINE-FREE HERBAL TEA*** Mountain Mel s Essential Goods, LLC…
    Category
    Food
    Distribution
    3 states