State
73,722 recalls have nationwide distribution and so reach Washington. 8,535 additional recalls listed Washington specifically in their distribution scope.
Of the 8,535 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 2,404 (28%) are Severe.
Which agencies issued them
These figures cover only the 8,535 recalls whose distribution notice names Washington specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Micro Bird is recalling 75 model-year 2019 MB II buses because a grounding wire issue may cause a short circuit, increasing the risk of fire.
Keystone RV Company is recalling 2020 Hideout 290LHS recreational trailers because they were built with incorrect axles and tires, increasing the risk of a crash.
Dick's Sporting Goods is recalling Field & Stream Kayak Cradles because kayaks may fall off while driving, increasing crash risk.
The P2K Bunk Bed System motor in certain 2021 Coachmen Sportscoach and Forest River Georgetown motorhomes may fail, causing the bunk to fall while the vehicle is in motion. This increases the risk of injury or a crash.
Mercedes-Benz is recalling 2019 C 300 vehicles because the center console lock may not function properly, increasing injury risk in rear-end crashes.
Aston Martin is recalling specific 2017-2020 models because front seat air bag fasteners may not be tightened correctly, increasing injury risk.
General Motors is recalling 2018 Cadillac, Chevrolet, and GMC vehicles because a vacuum pump issue can reduce power brake assist, increasing stopping distance.
Jayco is recalling 2021 Jay Feather X213 trailers because incorrect tire and weight labels may lead to vehicle overloading.
Frito-Lay is recalling 50 count Flavor Mix trays due to potential undeclared milk. Consumers should stop eating the product and return it to the store.
The Protein Shoppe is recalling Red-E Tablets found to contain sildenafil, an unapproved drug for erectile dysfunction. The product was marketed without FDA approval.
Frito-Lay is recalling 10-count Lays sacks in 11 states due to a potential undeclared milk allergen.
Ford is recalling 2020 F-350 trucks with ambulance prep packages because incorrect rear axles were installed, creating a risk of tire blowouts.
Frito-Lay is recalling specific bags of Lay's Barbecue Flavored Potato Chips because they may contain undeclared milk.
Frito-Lay is recalling 18 count Flavor Mix sacks because they may contain undeclared milk. The product was distributed to retail and foodservice locations in 11 western states.
Gilster-Mary Lee Corp. is recalling specific brands of organic microwave popcorn because tempered glass pieces were found in the product.
Frito-Lay is recalling 1,236 bags of Classic Variety Mix and Classic Mix due to potential undeclared milk. The products were distributed to retail and foodservice channels in 11 western states.
Frito-Lay is recalling 54-count Classic Mix cube boxes because they may contain undeclared milk. The product was distributed to retail and foodservice channels in 11 states.
Frito-Lay is recalling 28-count Classic Cube Mix boxes because they may contain undeclared milk. The product was distributed to retail and foodservice channels in 11 western states.
Siemens is recalling Syngo.via RT Image Suite software due to a calibration offset error that could result in incorrect radiation dose or dose applied to the wrong location.
STIHL is recalling about 185,000 mini-cultivator attachments because the gearbox may be installed upside down, causing tines to rotate toward the operator and posing a laceration risk.
BMW is recalling approximately 312 certain 2020-2021 BMW models due to rearview camera software that may slightly obscure the rear view image, potentially increasing crash risk if drivers rely solely on the camera.
GE Healthcare is recalling 62 Discovery NM 630 systems because rotor bearing screws were found loose on the detector.
LivaNova is recalling 94 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.
ArthroCare Corporation is voluntarily recalling 15,559 units of Smith&Nephew SmartStitch PerfectPasser Connectors because a manufacturing error may cause the upper jaw to detach during use.
LivaNova is recalling 77 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.