State
73,817 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.
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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Cooper Tire & Rubber Co. is recalling specific tire models due to an incorrect belt rubber compound that may cause belt separation and loss of vehicle control.
Crate and Barrel is recalling Dakota wooden benches because they can tip over, posing a fall hazard. The company has received reports of injuries including broken bones and an amputation.
AP Racing is recalling 16.9oz bottles of Super 600 Brake Fluid because the labels are missing required DOT information regarding track-only use and fluid type.
Daimler Vans USA is recalling 2017 Mercedes-Benz and Freightliner Sprinter 3500 vehicles because the Crosswind Assist system may fail to activate automatic braking in strong crosswinds, increasing crash risk.
Pier 1 Imports is recalling decorative glass pumpkins because the wooden stems can detach, causing the glass to break and cut consumers.
Todd Snyder is recalling approximately 2,100 men's sweatshirts in the U.S. because they fail to meet federal flammability standards, posing a burn risk to users.
Hunter Fan Company is recalling Contempo ceiling fans because incorrect installation instructions may cause the light globe to fall, posing an impact injury hazard.
International Laboratories is recalling Pravastatin Sodium Tablets 40 mg because they were filled with Bupropion hydrochloride XL Tablets 300 mg.
Gadget Island, Inc. is recalling PapaZen 3300 capsules because they contain undeclared prescription drugs sildenafil, desmethyl carbodenafil, and tadalafil.
Gadget Island, Inc. is recalling Rhino 7 Platinum 5000 capsules because they contain undeclared active pharmaceutical ingredients and were marketed without FDA approval.
Gadget Island, Inc. is recalling Grande X 5800 capsules because they contain undeclared prescription drugs sildenafil, desmethyl carbodenafil, and tadalafil.
Gadget Island, Inc. is recalling FIFTY SHADES 6000 capsules because they contain undeclared active pharmaceutical ingredients sildenafil, desmethyl carbodenafil, and tadalafil.
Forest River is recalling 2016-2018 Berkshire XLT motorhomes because incorrect circuit breakers may cause excessive heat and increase the risk of a fire.
Hyundai is recalling 2018 Santa Fe Sport vehicles because a side curtain air bag component may detach during deployment, increasing injury risk.
East Manufacturing is recalling 2016-2018 Frame Dump trailers because cracks in the cross member may cause failure, increasing crash risk.
Honda is recalling specific 2010, 2016, and 2017 VT1300CX Fury motorcycles because missing welds on the fuel tank mounting bracket could cause fuel leaks and fire.
Won Industry Co. is recalling three unapproved Compressible Limb Therapy Systems because they have incorrect air compression level setups. The devices were distributed in Maryland, Texas, and Mexico.
Becton Dickinson is recalling Trypticase Soy Agar with 5% Sheep Blood plates because they are contaminated with Listeria monocytogenes. The affected lots are distributed worldwide.
Biosense Webster is recalling 185 SMARTABLATE RF System Generators because they may inadvertently deliver RF energy if the foot pedal is placed near Stereotaxis magnets.
Becton Dickinson is recalling 2,598,000 BD Precision Glide Needles due to hub damage that can cause breakage or leakage during use.
Pro-Med Instruments is recalling DORO Sterile Disposable Skull Pins because two instances of pin tip breakage were reported during surgery.
Roche Diabetes Care is recalling the Accu-Chek Connect app because a bug in the Bolus Advisor feature may prevent correction bolus advice from being available for recent glucose readings.
Dominguez Family Enterprises is recalling Juanita's Brand OJOS Mexican Pastry due to undeclared coconut. The product was distributed in Oregon and Washington.
ICU Medical Inc is recalling MedNet 6.1 and 6.21 software because it may alter piggyback medication settings without user notice.
Biosense Webster is recalling PENTARAY NAV High-Density Mapping Catheters because the instructions for use were updated to indicate they should not be used in patients with prosthetic valves.