State
73,219 recalls have nationwide distribution and so reach Arizona. 8,387 additional recalls listed Arizona specifically in their distribution scope.
Of the 8,387 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 1,720 (21%) are Severe.
Which agencies issued them
These figures cover only the 8,387 recalls whose distribution notice names Arizona specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Prevost is recalling 2023 X3-45 and X3-45 VIP motor coaches because an insufficient grommet allows electrical cables to chafe, potentially causing a short circuit and fire.
Navistar is recalling 2016-2020 International and IC Bus models because an HVAC wiring terminal may overheat, increasing the risk of a fire.
General Motors is recalling certain 2003-2023 GMC Savana and Chevrolet Express Cutaway vehicles with optional rear HVAC systems. Exposed wiring and connectors can corrode and overheat, creating a fire risk.
Jaguar Land Rover North America is recalling certain 2022–2023 Land Rover Range Rover vehicles because the second-row left seat frame may have been insufficiently welded and may not adequately secure occupants during crashes or sudden braking.
Certain 2023 Land Rover Range Rover Sport vehicles have incorrect rear taillights and brake lights that do not illuminate correctly, reducing vehicle visibility. Dealers will replace the lights free of charge.
Monti Kids is recalling Basket with Balls toys sold in subscription boxes because the blue crocheted ball's sewn swirls can separate and expose small parts, creating a choking hazard for young children.
Nikola is recalling 2022-2024 TRE BEV trucks because the electronic parking brake may fail to engage, increasing the risk of a crash.
IKEA is recalling about 25,000 BLÅVINGAD fishing games because a small metal rivet in a wooden play piece can come loose and pose a choking hazard to young children. Four incidents have been reported globally, with none in the U.S. requiring medical attention.
BISSELL is recalling about 2,000 Cordless Multi-Surface Wet Dry Vacuums (models 2551R and 25518) because the battery pack circuit board can overheat and smoke, creating a fire hazard. No injuries have been reported.
THE ISH COMPANY is recalling 355 ISH Shrimpish Sample Meal Kits distributed to multiple states throughout 2022 for undeclared soy protein that may cause allergic reactions in sensitive consumers.
New Flyer is recalling 2023 XD60 and XDE60 buses because the anti-lock brake system may lose power during hard braking, increasing crash risk.
Maserati is recalling 2023 MC20 Cielo vehicles because insufficient windshield frame bonding could allow the frame to detach in a crash, increasing injury risk.
Porsche is recalling 2004-2005 Carrera GT vehicles because suspension joints may fail, increasing crash risk. Owners should not drive until repaired.
Over 127,000 disposable tourniquet cuffs are being recalled because they may fail to achieve or maintain pressure during surgery due to fabric tearing or O-ring defects, risking operative bleeding and hemorrhage.
Kawasho Foods USA is recalling Geisha Medium Shrimp 4 oz cans due to leaking and bulging containers. The defect may compromise food safety.
Ascend Laboratories is recalling 13,560 bottles of Dabigatran Etexilate 75 mg capsules nationwide because testing detected N-nitroso-dabigatran impurity levels above acceptable limits. The issue stems from a manufacturing quality control deviation.
Defibtech is recalling 29 units of the DDU-100 Lifeline AED due to an untested component that could cause device failure. The affected device may not deliver therapy if a malfunction occurs.
Preat Corp is recalling Neodent GM X 6mm titanium base components due to a dimensional defect causing vertical movement. This instability may lead to abutment fracture and potential ingestion of dental materials by patients.
Endo Pharmaceuticals is recalling Calcitonin Salmon Nasal Spray due to out-of-specification impurities and subpotent drug content. Affected lots distributed nationwide have expiration dates ranging from March 2023 to March 2025.
Entopsis, Inc. is recalling PCRopsis Reagent RVD-RT diagnostic kits due to misleading label statements that could affect proper use and test interpretation.
GaGa Pro Lighting Equipment Co. manufactures Class IV Laser Light Show projectors that are being recalled due to non-compliance with FDA's Performance Standard for laser products. Eleven units distributed nationwide are affected.
Covidien is recalling Shiley Lo-Pro Oral/Nasal Tracheal Tubes due to potential leaks in the inflation system. The affected devices, used during anesthesia and procedures, may not maintain proper airway sealing.
Ascend Laboratories is recalling 12,804 bottles of Dabigatran Etexilate 150mg capsules nationwide due to detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake limit caused by manufacturing process deviations.
Baxter Healthcare Corporation is recalling 16 Automated Peritoneal Dialysis Systems due to incomplete electrical safety testing. Affected devices require additional testing.
Direct Rx is recalling Ropinirole 1 mg tablets nationwide due to manufacturing process deviations. Consult a pharmacist before stopping this medication.