The Recall Desk

State

Washington product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7626–7650 of 81448

  • HighFDA (Devices)·Z-1462-2025·2025-04-02

    Medline Surgical Procedure Kits Recalled for Defective Plastic Syringes

    Medline Industries is recalling 1,228 surgical procedure kits containing defective plastic syringes. The syringes may leak or break during use, potentially affecting patient safety.

    Product
    Medline procedure kits labeled as: 1) BREAST PACK-LF, Pack Number DYNJ0956628O; 2) BREAST SURGERY FOAKS, Pack Number DYNJ63577C; 3) CHEST BREAST -LF, Pack Number DYNJCEN04C; 4) DIEP PACK, Pack Number DYNJ60669G; 5) FACE LIFT PACK, Pack Number DYNJ64670B; 6) FREE FLAP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1411-2025·2025-04-02

    Baxter surgical table software issue blocks emergency back adjustment

    Baxter is recalling 112 units of the TruSystem 7500 surgical table due to a software issue preventing upper back adjustment during emergency mode. No injuries have been reported.

    Product
    Baxter Floor mounting column TruSystem 7500, Product Code 1717021
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1450-2025·2025-04-02

    Medline Medical Procedure Kits With Plastic Syringes Recalled for Quality Issues

    Medline medical procedure kits containing plastic syringes are being recalled due to identified leaks, breakage, and quality issues that may pose a risk to patient health.

    Product
    Medline procedure kits labeled as: 1) L S GYN PACK, Pack Number DYNJ65616C; 2) MAIN CYSTO, Pack Number DYNJ61371A; 3) OB PACK-LF, Pack Number DYNJ20720C; 4) PELVISCOPY PACK-LF, Pack Number DYNJ0415776N; 5) POSTERIOR EYE PACK-LF, Pack Number PHS656483I; 6) ROBOTICS PA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1444-2025·2025-04-02

    Medline surgical procedure kits recalled for syringe leaks and breakage

    Medline procedure kits containing plastic syringes are recalled due to identified leaks, breakage, and quality issues that may pose a risk to patient health. The affected kits were distributed nationwide in the US and Canada.

    Product
    Medline procedure kits labeled as: 1) A & A KNEE PACK-LF, Pack Number DYNJHS0136D; 2) ABD CLOSURE PACK, Pack Number DYNJ56987B; 3) ADULT PERC PACK-LF, Pack Number PHS170994005A; 4) BASIC PACK, Pack Number DYNJ54836B; 5) BASIC PACK, Pack Number DYNJ58678A; 6) BASIC PACK, Pa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1416-2025·2025-04-02

    Baxter TruSystem 7500 Hybrid medical device software defect in emergency mode

    Baxter is recalling 2 units of TruSystem 7500 Hybrid (MC) due to a software issue that disables the upper back section adjustment when emergency mode is activated.

    Product
    Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1408-2025·2025-04-02

    Premier Solo Diamond dental burs recalled due to material hardness defect

    Premier Dental Products Co is recalling Premier Solo Diamond Large dental burs because the material hardness does not meet specifications and may cause the burs to bend during use. 77 units in six U.S. states are affected.

    Product
    Premier Solo Diamond - Large Invented Cone; SKU: 807016C.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0303-2025·2025-04-02

    Sodium Bicarbonate Injection Recalled Due to Sterility Assurance Issue

    Exela Pharma Sciences is recalling Sodium Bicarbonate 8.4% Injection due to lack of sterility assurance. The recall affects approximately 103,950 vials nationwide.

    Product
    SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0294-2025·2025-04-02

    Testosterone Gel Recalled Nationwide Due to Benzene Contamination

    Strides Pharma is recalling Testosterone Gel 1% nationwide due to the presence of benzene, a toxic substance. Patients should contact their healthcare provider about alternative treatment options.

    Product
    TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1443-2025·2025-04-02

    Medline CV Neonatal Procedure Kits Recalled Due to Syringe Quality Issues

    Medline is recalling CV Neonatal Pack procedure kits (Pack Number DYNJ67356) because the plastic syringes may leak or break, potentially harming patients. The recall affects 96 units distributed nationwide and in Canada.

    Product
    Medline procedure kits labeled as: 1) CV NEONATAL PACK, Pack Number DYNJ67356
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1433-2025·2025-04-02

    NexGen LPS Flex knee prosthesis recalled for labeling inconsistency

    Zimmer recalls 76 NexGen LPS Flex knee prosthesis units due to conflicting plate compatibility information on the product label.

    Product
    NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis, Model Number 00-5962-042-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1432-2025·2025-04-02

    Orthofix Pillar SA Ti Spacer System Mislabeled for Anterior Height

    Orthofix is recalling Pillar SA Ti Spacer System spinal implants because the product label lists an incorrect anterior height of 10mm, while the actual device measures 10.5mm. This labeling discrepancy could affect surgical planning during implantation.

    Product
    Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device, sterile, implant grade titanium alloy: (1) REF 82-3300SP, 33mm W x 24mm D x 10mm H, 7 degrees; (2) REF 82-3700SP, 37mm W x 28mm D x 10mm H, 7 degrees; and (3) REF 82-4000SP, 40mm W x 32mm D x 10mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1412-2025·2025-04-02

    Baxter Mobile Column TruSystem 7500 Software Defect Prevents Back Adjustment

    Baxter Healthcare is recalling the Mobile column TruSystem 7500 due to a software issue that prevents the upper back section from being adjusted when emergency mode is enabled. Approximately 1,596 units distributed nationwide are affected.

    Product
    Baxter Mobile column TruSystem 7500, Product Code 1717023
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0668-2025·2025-04-02

    Dried Lily Flowers Recalled Due to Undeclared Sulfites

    U.S. Trading Company recalled dried lily flowers due to undeclared sulfites, which pose a risk to people with sulfite sensitivity. The recall affected 5,200 packages distributed across 32 states and was terminated July 1, 2025.

    Product
    DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocallis citrina) Distributed by: U.S. TRADING COMPANY Hayward, CA 94545-1130 Product of China
    Category
    Food
    Distribution
    30 states
  • SevereNHTSA·25V203000·2025-04-01

    Gillig Recalls 2023-2024 Low Floor Buses Due to Battery Fire Risk

    Gillig is recalling 2023-2024 Low Floor transit buses because loose battery hardware may cause short circuits, increasing the risk of fire or loss of drive power.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V204000·2025-04-01

    Bollinger Motors Recalls 2025 B4 Trucks Due to Battery Seal Defect

    Bollinger Motors is recalling 2025 B4 trucks because the high-voltage battery pack may be improperly sealed, allowing liquid entry that could cause fire, shock, or loss of drive power.

    Product
    BOLLINGER MOTORS — BOLLINGER MOTORS B4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V202000·2025-04-01

    2025 BMW vehicles recalled for loose starter-generator connection defect

    BMW is recalling certain 2025 BMW vehicles because the electrical connection between the starter-generator and battery may come loose, potentially causing engine stall or fire.

    Product
    BMW — BMW 430I, 330I, X3, 430I XDRIVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E022000·2025-03-31

    Our Next Energy Recalls Aries LFP Battery Packs for Commercial Trucks

    Our Next Energy is recalling Aries LFP battery packs for commercial trucks because improper sealing may allow liquid entry, increasing the risk of fire or shock.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·PHA-03312025-01·2025-03-31

    USDA Issues Public Health Alert for White Chicken Chili Imported Without Inspection

    USDA FSIS issued a public health alert for Allen Family Foods White Chicken Chili imported from Canada without required reinspection. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert for White Chicken Chili Imported Without the Benefit of Import Reinspection
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·25V198000·2025-03-28

    Ford 3.5L engines can leak oil rapidly from misaligned cup plug

    Ford is recalling certain 2024-2025 F-150, Expedition and 2024 Lincoln Navigator vehicles with 3.5L GTDI engines because a misaligned engine cup plug can cause a rapid oil leak.

    Product
    FORD — FORD, LINCOLN EXPEDITION, F-150, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V199000·2025-03-28

    Ford Recalls 2025 F-150 Hybrid Vehicles Due to Fuse Defect

    Ford is recalling 2025 F-150 Hybrid vehicles because an incorrect fuse in the high-voltage battery junction box may fail, causing a sudden loss of drive power.

    Product
    FORD — FORD F-150 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V200000·2025-03-28

    Great Dane Recalls 2025-2026 Champion Trailers Due to Tire Defect

    Great Dane is recalling 2025-2026 Champion Dry Van trailers equipped with specific Bridgestone tires that may fail due to incorrect manufacturing.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·009-2025·2025-03-28

    Cargill Recalls Liquid Egg Products Due to Unapproved Cleaning Solution

    Cargill Kitchen Solutions is recalling approximately 212,268 pounds of liquid egg products that may contain a cleaning solution with sodium hypochlorite.

    Product
    Cargill Kitchen Solutions, Inc. — Cargill Kitchen Solutions Recalls Liquid Egg Products Due to an Unapproved Substance
    Category
    Food
    Distribution
    Distributed nationwide