The Recall Desk

State

Washington product recalls

73,596 recalls have nationwide distribution and so reach Washington. 8,466 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,466
Critical
865
Severe
2,399
Most recent
2026-10-21

Of the 8,466 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 2,399 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,466 recalls whose distribution notice names Washington specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27451–27475 of 82062

  • SevereFDA (Food)·F-0478-2021·2021-05-12

    Bueno Coffee Substitute Recalled for Undeclared Peanut and Barley

    Creative Foods Inc. is recalling Bueno Coffee Substitute Pecan Praline because it contains undeclared peanut and barley, posing a risk to individuals with allergies or celiac disease.

    Product
    Bueno Coffee Substitute Pecan Praline, Gluten-Free, net wt. 7 oz. (200g), UPC 6 79345 10010 4. INGREDIENTS: Simply Garbanzo Beans and Natural Flavoring. Manufactured By: Creative Foods, Inc. Prineville, Oregon. Bueno Coffee Substitute Pecan Praline, Gluten-Free, net wt. 3…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0358-2021·2021-05-12

    FDA Recalls Acetaminophen in Health Kits Due to Labeling Error

    A-S Medication Solutions is recalling Health Essentials Kits containing Acetaminophen 500mg tablets. The bottles were incorrectly labeled with prescription drug labels instead of OTC labels.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V342000·2021-05-12

    BMW Recalls 2021 230i and M240i for Roof Liner Support Defect

    BMW is recalling 2021 230i and M240i vehicles because roof liner supports may detach and fall into the cabin, increasing injury risk during a crash.

    Product
    BMW — BMW 230I, M240I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0480-2021·2021-05-12

    Hostess SnoBalls Recalled for Undeclared Coconut Allergen

    Hostess Brands is recalling SnoBalls snack cakes packaged with Chocolate CupCakes labels because the packaging fails to declare the major food allergen coconut.

    Product
    Hostesss SnoBalls packaged as Hostess Chocolate CupCakes, Net Wt 3.17 OZ, UPC 8 88109 01001 0, Hostess Brands, LLC Kansas City, MO
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-1534-2021·2021-05-12

    Greiner Bio-One Recalls VACUETTE Blood Collection Tubes for Insufficient Draw Volume

    Greiner Bio-One is recalling VACUETTE blood collection tubes because insufficient draw volume may cause erroneous coagulation test results.

    Product
    VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged - Product Usage: indicated for use in collection and transport of venous whole blood for coagulation testing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1533-2021·2021-05-12

    GE Healthcare Recalls Centricity Universal Viewer for Patient Data Mismatch Risk

    GE Healthcare is recalling 112 units of Centricity Universal Viewer software because a specific configuration may display comparison exams from the wrong patient.

    Product
    Centricity Universal Viewer - Product Usage: intended to assist in the viewing, analysis, diagnostic interpretation, and sharing of images and other information.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V341000·2021-05-12

    2021 Porsche Cayenne GTS Engine Cylinder Bore Crack Recall

    Porsche is recalling 2021 Cayenne GTS vehicles due to engine cylinder bore cracks that may cause engine damage, stalling, or oil leaks, increasing the risk of a crash or fire. Dealers will replace the engine at no charge.

    Product
    PORSCHE — PORSCHE CAYENNE GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V343000·2021-05-12

    2021 Gulf Stream Travel Trailers Recalled for Incorrect Tire Pressure Labels

    Gulf Stream is recalling certain 2021 travel trailers because the Federal Certification Label lists incorrect tire size and pressure information. Overinflated tires increase the risk of crashes.

    Product
    GULF STREAM — GULF STREAM VINTAGE CRUISER, GEO, NORTHERN EXPRESS, MATRIX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21133·2021-05-12

    Briggs & Stratton Recalls Log Splitters Due to Engine Kickback Injury Hazard

    Briggs & Stratton is recalling YTL, Longli, and TIYA log splitters with 250cc engines due to a kickback hazard that caused two broken wrists.

    Product
    YTL, Longli and TIYA Log Splitters with Briggs & Stratton® 250cc engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V344000·2021-05-12

    2021 Airstream Interstate Nineteen bus bar electrical fire hazard

    Airstream is recalling certain 2021 Interstate Nineteen motorhomes due to potentially incorrectly wired bus bar circuit breakers that may overheat and create a fire risk. Dealers will relabel and relocate the affected wires free of charge.

    Product
    AIRSTREAM — AIRSTREAM INTERSTATE NINETEEN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V345000·2021-05-12

    2020-2021 Airstream Travel Trailers Recalled for Fire Risk from Incorrectly Installed Stove

    Airstream is recalling certain 2020 and 2021 Flying Cloud and International travel trailers because the stove was incorrectly installed in a non-sealed cabinet. Drafts can force flames into the cabinet, creating a fire hazard.

    Product
    AIRSTREAM — AIRSTREAM INTERNATIONAL, FLYING CLOUD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1532-2021·2021-05-12

    Medtronic Abre Venous Self-expanding Sent System Recall for Incorrect Size Labeling

    Medtronic is recalling 23 Abre Venous Self-expanding Sent Systems because the device size is incorrectly printed on the device itself, though the packaging is labeled correctly.

    Product
    Medtronic Abre Venous Self-expanding Sent System, Catalog number REF AB9U16080090 - Product Usage: intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0479-2021·2021-05-12

    Natrol Melatonin 3 mg Tablets Recalled for Mislabeling as ALA 300 mg

    Natrol LLC is recalling one lot of Melatonin 3 mg tablets that were mislabeled as ALA 300 mg capsules. The recall covers 12,740 units distributed across multiple US states and international locations.

    Product
    Natrol Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap. Fall asleep faster, Stay asleep longer, 100$ Drug Free 1 Tablet 20 minutes before bedtime. Manufactured by Natrol LLC. Chatsworth, CA 91311 USA
    Category
    Drug
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-1529-2021·2021-05-12

    LeMaitre Vascular Recalls LeverEdge Contrast Injectors Due to Packaging Particulates

    LeMaitre Vascular is recalling 616 LeverEdge Contrast Injectors because particulates in the packaging foam could contaminate the sterile field.

    Product
    LeverEdge Contrast Injector: 35 cc syringe with ISO 594 female luer lock - Product Usage: intended to be used to perfuse contrast medias into the vessels for angiographic procedures, Catalog #: 4100-00.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1521-2021·2021-05-12

    Oto Med Recalls SpineX Bone Dust Collectors Due to Sterile Pouch Defects

    Oto Med Inc is recalling 415 SpineX Bone Dust Collectors because holes were found in the sterile Tyvek pouches during internal testing.

    Product
    Grace Medical REF S-4500 *** spineX BONE DUST COLLECTOR *** 2 stainless steel filters - Product Usage: intended to be inserted into a suction tube during the early stages of otologic surgery to collect bone particles for future use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1520-2021·2021-05-12

    Oto Med Recalls Bone Dust Collectors Due to Sterile Pouch Defects

    Oto Med Inc is recalling 5,092 Grace Medical Cox Bone Dust Collectors because holes were found in the sterile Tyvek pouches during internal testing.

    Product
    Grace Medical REF S-3500 *** COX BONE DUST COLLECTOR *** 2 stainless steel filters - Product Usage: intended to be inserted into a suction tube during the early stages of otologic surgery to collect bone particles for future use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1519-2021·2021-05-12

    Oto Med Recalls Sheehy Bone Dust Collectors Due to Packaging Defects

    Oto Med Inc is recalling 13,335 Sheehy Bone Dust Collectors because holes were found in the sterile Tyvek pouches during internal testing.

    Product
    Grace Medical REF S-2500 *** SHEEHY BONE DUST COLLECTOR *** Stainless steel filter - Product Usage: intended to be inserted into a suction tube during the early stages of otologic surgery to collect bone particles for future use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0474-2021·2021-05-12

    Thai Home Sweet Chili Paste Recalled for Acidified Food Rule Violations

    Jansala & Foods LLC is recalling Thai Home Sweet Chili Paste for failing to follow acidified food regulations. The product was distributed to retailers in California, Oregon, and Washington.

    Product
    Thai Home brand Sweet Chili Paste (Num Prik Pao) packaged in glass jars. Net weight 6.5 oz (180g). Refrigerate after opening. UPC 8616080004054 Manufactured by: Jansala & Foods LLC 1813 NE 2nd Avenue Portland, OR [email protected] Distributed by: Earthly Gourmet…
    Category
    Food
    Distribution
    3 states