State
72,982 recalls have nationwide distribution and so reach Arizona. 8,381 additional recalls listed Arizona specifically in their distribution scope.
Of the 8,381 recalls naming Arizona we have scored against our rubric, 1,313 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,717 (20%) are Severe.
Which agencies issued them
These figures cover only the 8,381 recalls whose distribution notice names Arizona specifically. The 72,982 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Keystone is recalling 2025 Carbon, Fuzion, and Raptor toy haulers because missing rear gate pins or leg support brackets may allow the gate to shift, increasing injury risk.
Kawasaki is recalling 2025 W230 ABS motorcycles because an unstable electrical ground connection may cause the engine to stall, increasing crash risk.
Forest River is recalling certain 2025-2026 Wildwood and Salem travel trailers because the exterior transit latch on the rear patio door cannot be unlocked from inside the vehicle.
Forest River is recalling certain 2026 Spirit travel trailers because the installed safety chains may not meet the actual Gross Vehicle Weight Rating, posing a risk of trailer separation from the tow vehicle.
Kia is recalling 2020-2022 Niro EV vehicles because a damaged rearview camera circuit board may prevent the image from displaying, increasing crash risk.
Forest River is recalling 2026 Sabre fifth wheel recreational trailers because the exterior griddle may be incorrectly installed, allowing it to be stowed while still connected to LPG, increasing fire risk.
Subaru is recalling certain 2025 Forester vehicles because the child seat anchor bolts may have been improperly tightened, allowing them to come loose.
Honda is recalling 2013 Accord vehicles with 4-cylinder engines and CVTs in 23 states and D.C. because the driveshaft may corrode and break, potentially causing a loss of drive power or vehicle rollaway.
Vanguard is recalling 2021-2023 VXP 28-Foot Pup trailers because the pintle hook box assembly may crack or break, reducing stability while being towed.
Supreme is recalling 2025 Wabash trucks because insufficient lubrication on the liftgate pin may cause it to seize, leading to liftgate failure and injury risk.
Shyft Group is recalling 2024-2025 Utilimaster Aeromaster vehicles because the 360-degree camera monitor may not display the correct image at startup, increasing crash risk.
Alembic Pharmaceuticals is recalling Celecoxib 200 mg capsules after a customer found a Tadalafil 5 mg tablet inside a sealed 500-count bottle. The contamination was discovered through a customer complaint.
Philips is recalling three Intera 1.5T Achieva Nova-Dual MRI systems worldwide due to a gradient coil component failure that can generate smoke and fire, posing risks including burn injury and asphyxia.
Zyno Medical LLC is recalling 613 units of the Z-800 Infusion System distributed nationwide because unreleased software versions were installed on the devices without verification or validation.
Lipman Family Farms is recalling Cucumber 5lb cases distributed across 18 states due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it to the retailer.
Amneal Pharmaceuticals is recalling Sulfamethoxazole and Trimethoprim Tablets (400 mg/80 mg) nationwide due to microbial contamination that may cause black spots on tablets. The contamination affects non-sterile products distributed across the USA.
Philips SmartPath to dStream for 1.5T MRI systems are recalled due to potential gradient coil component failure that may produce smoke and fire, posing risks of inhalation injury, burns, asphyxia, and death.
Philips is recalling certain Intera Achieva 1.5T Pulsar MRI systems due to a potential component failure in the gradient coil that could generate smoke and/or fire, risking patient and operator injury or death.
Tecfen Medical is recalling its 20G (1.2mm) MVR Sideport Knife Straight (Model QKN2312) ophthalmic knives due to sterility assurance concerns. The recall affects 38 units distributed in the US and internationally.
Tecfen Medical is recalling 2.8mm Slit Knife, Angled (Model QKN2808) ophthalmic surgical instruments due to sterility assurance concerns. Affected units were distributed in the US and internationally.
Mazda is recalling certain CX-50 Hybrid and CX-50 vehicles because incorrectly configured module software may cause the airbag to deploy improperly. All affected vehicles are under dealer control.
Philips is recalling certain Intera 1.5T Achieva Nova MRI systems due to a gradient coil component that can overheat, potentially causing smoke or fire with risk of burns, smoke inhalation, or asphyxia.
Male Ultra Pro capsules are being recalled because laboratory testing found undeclared propoxyphenylsildenafil and sildenafil. The product was marketed without an approved New Drug Application.
Lipman Family Farms is recalling Cucumber Super Selec products due to potential Salmonella contamination. The affected cucumbers were distributed across multiple states.
Philips is recalling one Intera 1.5T Explorer/Nova Dual MRI system due to a gradient coil component that may overheat, produce smoke, or ignite, risking patient and operator injury.