The Recall Desk

State

Washington product recalls

72,940 recalls have nationwide distribution and so reach Washington. 8,456 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,456
Critical
867
Severe
2,006
Most recent
2026-09-09

Of the 8,456 recalls naming Washington we have scored against our rubric, 867 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,006 (24%) are Severe.

These figures cover only the 8,456 recalls whose distribution notice names Washington specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3101–3125 of 81396

  • HighFDA (Devices)·Z-1457-2026·2026-03-04

    Olympus resection sheath recalled after reports of ceramic tip breaking

    Olympus is recalling its Resection Sheath model A2666T, used for endoscopic diagnosis and treatment in urological applications, after complaints that the ceramic tip of the sheath can break.

    Product
    Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1466-2026·2026-03-04

    Medline apheresis and central line kits recalled over connector seal defects

    Medline is recalling Apheresis Subqport Access Kits and Central Line Insertion kits containing Tego Connectors because the silicone seal may dome or tear, which can occlude the fluid path or allow leakage.

    Product
    Medline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU DYNDA2705 Medline CENTRAL LINE INSERTION SKU DYNJ63347A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0532-2026·2026-03-04

    Frozen Fish Balls Recalled Due to Undeclared Wheat and Sesame

    Min Jiang Food Store Inc is recalling frozen fish balls because they contain undeclared wheat and sesame, which are common allergens.

    Product
    Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt. UPC# 810093891320
    Category
    Food
    Distribution
    8 states
  • HighFDA (Drugs)·D-0351-2026·2026-03-04

    Bio Glo fluorescein strips 300-count recalled over sterility assurance failure

    Wizcure Pharmaa is recalling all lots of Bio Glo Fluorescein Sodium Ophthalmic Strips in 300-strip packs because the products were not manufactured in conformance with current good manufacturing practices.

    Product
    Bio Glo Fluorescein Sodium Ophthalmic Strips USP, 300 diagnostic strips, Manufactured Omni Lens Pvt Ltd 5 - Samruddhi, Opp. Sakar - III, Navrangpura, Ahmedabad - 380014, India, Email:[email protected], Manufactured for & distributed by: HUB Pharmaceuticals, LLC, 8767 E Via de Ven
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0346-2026·2026-03-04

    Vista Tears lubricant eye drops recalled over sterility assurance failure

    Wizcure Pharmaa is recalling all lots of Vista Tears Polyethylene Glycol 400 and Propylene Glycol eye drops because the products were not manufactured in conformance with current good manufacturing practices.

    Product
    Vista Tears Polyethylene Glycol 400 0.4% w/v, Propylene Glycol 0.3% w/v Eye Drops, Dry Eye Relief, Lubricant Drops, Sterile 10 ml (1/3 fl. oz.), Manufactured by: RA/Drugs/ MFG/2019/196283, Omni Lens Pvt. Ltd. 5, Samrudhhi, Opposite:Sakar-III, Navrangpura, Ahmedabad-380014, INDIA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V125000·2026-03-04

    Audi Recalls 2019 A6, A7, and Q8 for Lane Departure Software Error

    Volkswagen Group of America is recalling 2019 Audi A6, A7, and Q8 vehicles because a software error may deactivate the lane departure warning system.

    Product
    AUDI — AUDI A6, A7, Q8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0529-2026·2026-03-04

    Grape gummy candy recalled for containing unallowed color Carmoisine E122

    SB Food LLC is recalling Yoyo Gummy Grape Plus Flavor, 2.8 oz bags, because the products contain an unallowed color, Carmoisine (E122) - Acid Red 14.

    Product
    Yoyo Gummy Grape Plus Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-1441-2026·2026-03-04

    Olympus resection sheath recalled due to ceramic tip breakage

    Olympus is recalling 3,484 Resection Sheaths, Model A22041A, after receiving complaints that the ceramic tip can break during urologic procedures. The recall covers all lots distributed nationwide.

    Product
    Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1462-2026·2026-03-04

    Edermy PIE PAK units recalled for lacking FDA 510(k) clearance

    Edermy LLC is recalling PIE PAK models P2HC-A, P2HC-S and P2HC because the devices lack 510(k) clearance from the FDA.

    Product
    PIE PAK Models: P2HC-A, P2HC-S, P2HC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0528-2026·2026-03-04

    FDA Recalls Yoyo Gummy Tropical Flavor Candy for Unauthorized Color Additive

    SB FOOD LLC is recalling Yoyo Gummy Tropical Flavor candy because it contains Carmoisine (E122), a color additive not approved for use in this product. The recalled product was distributed to 15 states.

    Product
    Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-1472-2026·2026-03-04

    Adapt Pump Medical Device Recalled Due to Microclimate Management Function Failure

    Agiliti Health - Ellis is recalling Adapt Pumps (Model 61600200) because the Microclimate Management function may fail to re-engage after using the Autofirm function.

    Product
    Adapt Pump, Model/Catalog Number: 61600200-Adapt Pump, component of Adapt support surfaces (Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, Adapt Convertible EX), sofware version 1.3.0; Mattress, Air Flotation, Alternating Pressure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0527-2026·2026-03-04

    Yoyo Gummy Assorted Flavor Recalled Due to Unallowed Color Additive

    SB FOOD LLC is recalling Yoyo Gummy Assorted Flavor because the product contains Carmoisine (E122) - Acid Red 14, which is an unallowed color.

    Product
    Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
    Category
    Food
    Distribution
    15 states
  • LowFDA (Drugs)·D-0343-2026·2026-03-04

    Eptifibatide Injection Labeling Error Recall by Slate Run

    Slate Run Pharmaceuticals is recalling Eptifibatide Injection due to a labeling error on the carton, which incorrectly describes the dosing instructions.

    Product
    EPTIFIBATIDE — EPTIFIBATIDE (EPTIFIBATIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2026-EXP·2026-03-03

    Ajinomoto Recalls Chicken and Pork Fried Rice Due to Glass Contamination

    Ajinomoto Foods North America is expanding a recall for frozen fried rice, ramen, and shu mai products due to possible glass contamination. No injuries have been reported.

    Product
    Ajinomoto Foods North America — Ajinomoto Foods North America, Inc. Expands Recall for Chicken and Pork Fried Rice, Ramen, and Shu Mai Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·26V123000·2026-03-03

    Lincoln Corsair and Ford vehicles recalled for rearview camera display issues

    Ford Motor Company is recalling certain 2020-2024 Lincoln and Ford vehicles because the center display may show an inverted rearview image, increasing crash risks.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER, ESCAPE, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V122000·2026-03-03

    2025 Ford Vehicles Recalled for EGR Valve Failure Risk

    Ford is recalling certain 2025 vehicles due to a potential EGR valve failure that could cause an unexpected loss of drive power, increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR, RANGER, MUSTANG, MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V120000·2026-03-03

    Ford Recalls 2026 Lincoln Navigator for Driver Seat Software Defect

    Ford is recalling 2026 Lincoln Navigator vehicles because the driver seat software may malfunction at low speeds, causing the seat to move unexpectedly and increasing crash risk.

    Product
    LINCOLN — LINCOLN NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V117000·2026-03-03

    Ford and Lincoln vehicles recalled due to windshield wiper motor failure risk

    Ford Motor Company is recalling certain 2020-2022 Ford and Lincoln vehicles because the windshield wiper motors may fail, potentially reducing visibility and increasing crash risks.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR, AVIATOR, EXPLORER, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V124000·2026-03-03

    Ford Bronco and Edge Vehicles Recalled for Camera Software Issue

    Ford is recalling certain 2021-2026 Bronco and 2021-2024 Edge vehicles because the rearview camera may fail to display an image due to an overheating module.

    Product
    FORD — FORD BRONCO, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03012026-01·2026-03-01

    USDA Issues Public Health Alert for Punahele Beef Jerky Due to Undeclared Soy

    USDA FSIS issued a public health alert for Punahele beef jerky products containing undeclared soy lecithin. Consumers are advised not to consume the items.

    Product
    Punahele Jerky Company, Inc. — FSIS Issues Public Health Alert for Ready-To-Eat Beef Jerky Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalCPSC·26288·2026-02-26

    Trankerloop Baby Bath Seats Recalled Due to Drowning Risk

    Trankerloop is recalling approximately 2,380 baby bath seats because they are unstable and can tip over, posing a risk of serious injury or death from drowning.

    Product
    Trankerloop Baby Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide