The Recall Desk

State

Washington product recalls

73,809 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,536
Critical
865
Severe
2,405
Most recent
2026-11-04

Of the 8,536 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 2,405 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,536 recalls whose distribution notice names Washington specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39251–39275 of 82345

  • ModerateFDA (Devices)·Z-0766-2019·2019-01-30

    Stryker Recalls Reprocessed Diagnostic Electrophysiology Catheters Due to Chip Error

    Stryker is recalling 103 reprocessed diagnostic electrophysiology catheters because an EEPROM chip error may occur when used with CARTO navigation systems.

    Product
    BW Lasso 2515 ANV eco Variable Diagnostic EP Catheter, REF D134301 Diagnostic electrophysiology (EP) catheters are specially designed electrode catheters that transmit electrical impulses and can be positioned for endocardial recording or stimulation.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Drugs)·D-0430-2019·2019-01-30

    Heparin Injectable Solution Recalled for Incorrect Concentration Labeling

    Advanced Pharma Inc. is recalling Heparin Injectable Solution because the label incorrectly states the concentration as 50 mg/50 mL instead of 50 Units/50 mL.

    Product
    HEPERAIN 50 mg/50 mL (1mg/mL) Injectable Solution, Heparin Sodium 0.45% Sodium Chloride QS Heparin 50 Units 50 mL, Sterile single use syringe, Avella of Houston an FDA Registered 503B Outsourcing Facility 9265 Kirby Dr. Houston, TX 77054 (877) 794-0404 ---- NDC: 42852-725-65
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0390-2019·2019-01-30

    Lupin Recalls Fluocinolone Acetonide Topical Solution Due to Impurities

    Lupin Pharmaceuticals is recalling 24,180 bottles of Fluocinolone Acetonide Topical Solution due to elevated impurities.

    Product
    FLUOCINOLONE ACETONIDE — FLUOCINOLONE ACETONIDE (FLUOCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2019·2019-01-29

    Tyson Recalls Chicken Nuggets Due to Possible Rubber Contamination

    Tyson Foods is recalling approximately 36,420 pounds of chicken nuggets that may contain rubber. Consumers should not eat the product and should discard it or return it to the store.

    Product
    Tyson Foods, Inc. — Tyson Foods, Inc. Recalls Chicken Nugget Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V061000·2019-01-29

    Proterra Recalls 2015-2018 Catalyst Buses for Air Brake Moisture Risk

    Proterra is recalling 2015-2018 Catalyst 40 transit buses because missing air brake components may allow moisture buildup, potentially leading to brake failure.

    Product
    PROTERRA — PROTERRA CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V060000·2019-01-29

    Honda Recalls Acura and Honda Vehicles for Fuel Pump Defect

    Honda is recalling 2015-2019 Acura and Honda vehicles because fuel pump particulates may cause engine stalls, increasing crash risk.

    Product
    ACURA — ACURA, HONDA MDX, ACCORD, TLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·008-2019·2019-01-28

    Perdue Recalls Chicken Nuggets Due to Undeclared Milk Allergen

    Perdue Foods is recalling refrigerated chicken nuggets because they contain milk, a known allergen, that is not listed on the label.

    Product
    PERDUE FOODS, LLC. — Perdue Foods, LLC Recalls Refrigerated Fun Shapes Chicken Breast Nuggets Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    14 states
  • SevereNHTSA·19V059000·2019-01-28

    Gillig Recalls 2016-2018 Low Floor Buses for Steering Defect

    Gillig is recalling 2016-2018 Low Floor buses because a steering draglink ball stud may not be properly tightened, increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V058000·2019-01-28

    Keystone Montana Recalled for Kitchen Slide Bolt Tire Contact Risk

    Keystone RV is recalling 2019 Montana trailers because a kitchen slide adjustment bolt may contact the tire, potentially causing tire failure and increasing crash risk.

    Product
    KEYSTONE — KEYSTONE MONTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V055000·2019-01-28

    Stoughton Recalls 2016-2019 DVW Trailers Due to Cracking Hitch Points

    Stoughton is recalling 2016-2019 DVW trailers because the forward attachment points for the pintle mounting assembly may crack, potentially causing the trailer to detach from the tow vehicle.

    Product
    STOUGHTON — STOUGHTON DVW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V057000·2019-01-28

    Audi Recalls 2013-2016 A8 and S8 Models for Fuel Leak Risk

    Volkswagen Group of America is recalling 2013-2016 Audi A8 and S8 vehicles because a fuel supply line may leak, increasing the risk of fire.

    Product
    AUDI — AUDI A8, S8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V020000·2019-01-24

    Ram 1500 Recall: Improperly Secured Battery Ground Fastener

    Chrysler is recalling 2019 Ram 1500 vehicles because an improperly secured battery ground fastener may cause loss of power steering assist, increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V054000·2019-01-24

    Mack Trucks Recalls 2019-2020 Models Due to Detaching Mirror Risk

    Mack Trucks is recalling 2019-2020 Anthem, Granite, and Pinnacle vehicles because the passenger-side door mirror may detach, posing a risk of injury or crash.

    Product
    MACK — MACK PINNACLE (PI/PN), ANTHEM (AN), PINNACLE (CHU), GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V052000·2019-01-24

    Acura Recalls 2014-2019 ILX Vehicles for Fuel Tank Defect

    Acura is recalling 2014-2019 ILX vehicles because a deformed fuel tank may cause the fuel gauge to display inaccurate levels, potentially leading to stalling and crashes.

    Product
    ACURA — ACURA ILX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V049000·2019-01-23

    Spartan K1 Motor Home Chassis Recalled for Brake Component Defect

    Spartan is recalling 2019-2020 K1 motor home chassis because missing or improper cotter pins may cause brake actuator rods to detach, increasing stopping distance.

    Product
    SPARTAN — SPARTAN K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0724-2019·2019-01-23

    Arthrex Suture Anchor Recall Due to Potential Breakage During Insertion

    Arthrex is recalling Nano Corkscrew FT Suture Anchors because they may break during insertion. The recall covers 1,418 units distributed in the US and abroad.

    Product
    Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with needles.) Part Number AR-1317FT Product Usage: Soft tissue fixation to bone in the hand and wrist
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0750-2019·2019-01-23

    Kimberly-Clark Recalls U by Kotex Sleek Tampons for Structural Defect

    Kimberly-Clark is recalling U by Kotex Sleek tampons because they may come apart upon removal. The recall covers 68,852,076 units distributed nationwide and in Canada.

    Product
    U by Kotex¿ Sleek¿, Regular/Super Tampons, 34 Count Multipack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0735-2019·2019-01-23

    Zimmer Biomet Recalls Maximum Variable Pitch Compression Screw Caddy

    Zimmer Biomet is recalling 971 Maximum Variable Pitch Compression Screw Caddies due to a potential for silicone shedding during cleaning and sterilization.

    Product
    Maximum Variable Pitch Compression Screw Caddy, Reference Number 231201003 Product Usage: Intended to carry implants and instruments during regular inventory distribution and handling and sterilization in the hospitals
    Category
    Medical Device
    Distribution
    Distributed nationwide