State
72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 1,416 NorthStar hot water pressure washers are being recalled because the fan wheel can fail, causing abnormal burner operation that can produce smoke or bursts of flames.
About 9,150 LuxJet Submersible LED Lights are being recalled because the lithium coin batteries can be accessed easily by children and the lights lack the warnings required by Reese's Law.
About 21,170 bottles of Bazic Silicone Glue are being recalled because the methanol-containing glue is not in child-resistant packaging and is incorrectly labeled "Non-Toxic".
About 320 Urban Arrow FamilyNext Pro Cargo E-Bikes are being recalled because the Fidlock buckle can fail to fully latch when used with children in the cargo area.
About 21,230 Giraffe and Llama plush toys with clips sold at Hobby Lobby are being recalled because the legs can detach and release small beads.
About 148,370 Mindbodygreen Ultimate Multivitamin+ bottles are being recalled because the packaging holding iron-containing supplements is not child-resistant.
About 8,600 Viofairy Hair Growth Serum are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
About 19,890 rear wheel bolts on 2026 Trek FX+ 1 and Electra Townie Go! electric bicycles are being recalled because the bolts can break when torqued, causing wheel separation.
Winnebago is recalling 2026 Access travel trailers because the Gross Axle Weight Rating may be missing from the certification label, which could lead to overloading.
Autocar is recalling 2023-2026 Xpeditor vehicles because contact with the drive line yoke may damage the Electronic Stability Control unit, increasing crash risk.
About 600 Primark The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets are being recalled because the crayons have high levels of strontium and aluminum.
About 7,000 Sefudun 5% Minoxidil Hair Growth Serum Kit are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
White Castle System is recalling 1,021 cases of White Castle Original Sliders over undeclared milk and soy.
Medline is recalling 35,694 units of the Full Electric Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Zero Motorcycles is recalling 2024-2025 DS, DSR, DSRP, and DSR/X motorcycles because a twisted front brake hose may leak fluid and reduce braking ability.
Ducati is recalling certain 2025-2026 Streetfighter V4 and Panigale V4 motorcycles because excessive heat may damage the rear brake hose, resulting in a sudden loss of the rear brakes.
Merit Medical Systems is recalling 4,163,123 units of the Merit Medical Inflation Device basixCOMPAK because the inflation device handle may detach from the syringe during a procedure.
Mazor Robotics is recalling 549 Mazor X robotic guidance systems over software errors that can result in incorrect surgical instrument positioning during spinal surgery.
Zydus Pharmaceuticals is recalling 22,896 bottles of Icosapent Ethyl capsules, 1 gram, because oxidation caused by leakage of the capsule contents has left them subpotent.
Philips is recalling 228 Azurion systems on software version R3.1 over two software issues that may result in loss of imaging, loss of motorized movement, incorrect image content or loss of data.
ICU Medical is recalling 14,684,607 Tego Connectors because the silicone seal may bulge, separate from the body or tear, which can cause fluid leaks, occluded flow or air infused into the body.
GE HealthCare is recalling 364 Omni Legend PET systems because an intermittent issue can produce a streaking artifact in PET clinical scan images.
Baxter Healthcare is recalling 585 SIGMA Spectrum Infusion Pumps because defective grease on the cam and motor gears could lead to over-infusion or a free-flow situation.
RaySearch Laboratories is recalling RayStation/RayPlan model 10.1.1 because calculated radiation dose is not invalidated as intended for certain regions of interest.
Graviti Pharmaceuticals is recalling 4,212 bottles of Furosemide Tablets, USP 40 mg over the presence of a foreign substance.