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.

4101–4125 of 81396

  • ModerateFDA (Devices)·Z-0894-2026·2025-12-17

    Sacroiliac fusion screws recalled over labeling claims not consistently present

    Orthofix U.S. is recalling 19,431 FIREBIRD SI Fusion System units because the labeling contains claims that are not consistently present.

    Product
    Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model/Catalog Number: 18-1025SP 11mm X 25mm FIREBIRD SI Screw; 18-1030SP 11mm X 30mm FIREBIRD SI Screw; 18-1035SP 11mm X 35mm FIREBIRD SI Screw; 18-1040SP 11mm X 40mm FIREBIRD SI Screw; 18-1045S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0893-2026·2025-12-17

    PTC spacer implants recalled over labeling claims not consistently present

    Orthofix U.S. is recalling 13,317 Pillar SA PTC Spacer System units because the labeling contains claims that are not consistently present.

    Product
    Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System Model/Catalog Number: 39-9012SP 33W X 28L X 12.5H, 7DEG PTC IMPLANT; 39-9014SP 33W X 28L X 14H, 7DEG PTC IMPLANT; 39-9016SP 33W X 28L X 16H, 7DEG PTC IMPLANT; 39-9018SP 33W X 28L X 18H, 7DEG
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0891-2026·2025-12-17

    Mini PTC spacer implants recalled over labeling claims not consistently present

    Orthofix U.S. is recalling 61,977 CONSTRUX Mini PTC Spacer System units because the labeling contains claims that are not consistently present.

    Product
    Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number: 37-3106SP 12mm W X 12mm L, 6mm H, Parallel; 37-3107SP 12mm W X 12mm L, 7mm H, Parallel; 37-3108SP 12mm W X 12mm L, 8mm H, Parallel; 37-3109SP 12mm W X 12mm L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0217-2026·2025-12-17

    Lanthanum carbonate tablets recalled in a second hardness specification failure

    Cipla USA is recalling 1,180 boxes of Lanthanum Carbonate chewable tablets, 1000mg, from a further lot after an out of specification hardness test result.

    Product
    LANTHANUM CARBONATE — LANTHANUM CARBONATE (LANTHANUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0223-2026·2025-12-17

    Morphine sulfate oral solution recalled over a carton size mismatch

    Winder Laboratories is recalling 3,528 bottles of Morphine Sulfate Oral Solution because the size stated on the carton label did not match the size of the bottle inside.

    Product
    MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0919-2026·2025-12-17

    Hospital mattresses recalled because they are not tested with certain beds

    Stryker is recalling 297 Arise 1000EX mattresses because they and certain MV3 beds have been sold in close proximity, and the two products have not been tested for compatibility.

    Product
    Stryker Arise 1000EX mattress, Part Number 2236000000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0916-2026·2025-12-17

    Hybrid balloon pumps recalled with a revised preventative maintenance schedule

    Datascope is recalling 11,470 Cardiosave Hybrid Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.

    Product
    Cardiosave Hybrid. Intra-Aortic Balloon Pump system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0917-2026·2025-12-17

    Balloon pump systems recalled with a revised preventative maintenance schedule

    Datascope is recalling 47 Cardiosave Rescue Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.

    Product
    Cardiosave Rescue. Intra-Aortic Balloon Pump system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V869000·2025-12-16

    Toyota hybrid inverter bolt can loosen causing power loss or fire

    Toyota is recalling certain 2025-2026 Camry Hybrid and 2026 Corolla Cross Hybrid vehicles because a bolt inside the inverter may not be tightened properly, causing incomplete contact at the terminal.

    Product
    TOYOTA — TOYOTA CAMRY HYBRID, COROLLA CROSS HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V867000·2025-12-15

    Mack Trucks Recalls 2010-2016 Granite Trucks Due to Brake Imbalance Risk

    Mack Trucks is recalling 2010-2016 Granite trucks because incorrect parts from a previous repair may cause brake overheating, increasing the risk of tire blowouts or fires.

    Product
    MACK — MACK GRANITE (GU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V866000·2025-12-12

    Ford Super Duty trucks recalled over rear axle shafts that may break

    Ford is recalling 6,819 model year 2026 Super Duty F-250 and F-350 vehicles because the right rear axle shaft may have been improperly heat-treated and may break.

    Product
    FORD — FORD F-350 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V860000·2025-12-12

    Ford Recalls 2022-2025 E-Transit Vehicles Due to Axle Shaft Defect

    Ford is recalling 2022-2025 E-Transit vehicles because the left rear axle half shaft may disengage, causing loss of drive power or vehicle rollaway.

    Product
    FORD — FORD E-TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·038-2025·2025-12-12

    Suzanna's Kitchen Recalls Breaded Chicken for Undeclared Soy Allergen

    Suzanna's Kitchen is recalling fully cooked breaded chicken products because they contain soy, a known allergen, that is not declared on the label.

    Product
    Suzanna's Kitchen — Suzanna’s Kitchen Recalls Fully Cooked Breaded Chicken Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·25V865000·2025-12-12

    Mercedes-Benz wagons recalled over wiring harness routing near the front driveshaft

    Mercedes-Benz USA is recalling 117 AMG E 53 4MATIC+ Wagon vehicles because the transmission wiring harness may be routed too close to the front driveshaft, which can cause a loss of drive power.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG E 53 4MATIC+ WAGON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V862000·2025-12-12

    Ford Recalls 2025-2026 Corsair and Escape for Seat Belt Defect

    Ford is recalling 2025-2026 Corsair and Escape vehicles because rear seat belt retractors may not be securely fastened, increasing injury risk in crashes.

    Product
    FORD — FORD, LINCOLN ESCAPE, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V863000·2025-12-12

    Ford electric trucks and SUVs recalled over a park function failure

    Ford is recalling 272,645 F-150 Lightning, Mustang Mach-E and Maverick vehicles because the integrated park module may fail to lock into park when the driver shifts into park.

    Product
    FORD — FORD F-150 LIGHTNING BEV, MAVERICK, MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V858000·2025-12-11

    Honda Recalls 2025 CR-V Fuel Cell EVs for Fuel Cell Leak Risk

    Honda is recalling 2025 CR-V Fuel Cell EVs because coolant may leak into the fuel cell stack, causing an internal short circuit and loss of drive power.

    Product
    HONDA — HONDA CR-V FUEL CELL EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V859000·2025-12-11

    Honda Recalls 2016-2020 Acura ILX for Brake Master Cylinder Defect

    Honda is recalling 2016-2020 Acura ILX vehicles because contaminated brake fluid may deform a seal, causing an internal leak and reduced brake function.

    Product
    ACURA — ACURA ILX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26142·2025-12-11

    Garment steamers recalled after hot water leaks caused burn injuries

    About 2,840 VEVOR Garment Steamers are being recalled because they can leak or spit hot water. Reported cap failures resulted in two burn injuries, including a second-degree burn with permanent scarring.

    Product
    VEVOR Garment Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26146·2025-12-11

    Baby bath seats recalled because they are unstable and can tip over

    About 8,960 YCXXKJ baby bath seats are being recalled because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.

    Product
    YCXXKJ Baby Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide