State
73,570 recalls have nationwide distribution and so reach Arizona. 8,391 additional recalls listed Arizona specifically in their distribution scope.
Of the 8,391 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 2,047 (24%) are Severe.
Which agencies issued them
These figures cover only the 8,391 recalls whose distribution notice names Arizona specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
KTM is recalling 2019-2020 790 Adventure models because a weak front brake spring may reduce braking functionality, increasing the risk of a crash.
Tiffin Motorhomes is recalling 2017-2021 Bus and Phaeton vehicles due to fuel rail assembly defects that may leak, posing a fire risk. Owners should contact Tiffin customer service at 1-256-356-8661 for a free inspection.
Braun Northwest is recalling 2013-2020 NorthStar Ambulances because LCD displays may lock up, potentially delaying emergency efforts.
Modernist Pantry is recalling Kitchen Alchemy Sodium Hydroxide products because the packaging is not child-resistant and labels violate federal hazardous substance requirements.
Full Vision is recalling Rogers Brothers Rear Impact Guards because the steel may not meet specifications, potentially reducing strength and increasing injury risk in crashes.
American Honda is recalling 2021 CRF450R off-road motorcycles because the drive chain can break while in use, posing crash and injury hazards to the rider.
Real Water, Inc. is recalling Real Alkalized Water in various bottle sizes after the FDA was notified of cases of acute liver failure following consumption.
Real Water, Inc. is recalling Real Alkalized Water concentrate after FDA was notified of cases of acute liver failure following consumption.
Smiths Medical ASD Inc. is recalling specific lots of manifold rotators and related components because they may have insufficient or incomplete welds.
AngioDynamics is recalling specific Safe Sheath Ultralite kits due to potential sterility compromise. The recall affects 337 units distributed nationwide.
Smiths Medical ASD Inc. is recalling specific lots of Medex High Pressure Rotators because they may have insufficient or incomplete welds.
Heartware, Inc. is updating the Instructions for Use and Patient Manual for the HVAD System to clarify carrying case care, driveline cover orientation, and controller power-up sequences.
Smiths Medical ASD Inc. is recalling specific lots of Medex pressure injector lines and related components due to insufficient or incomplete welds.
BIOTRONIK Inc is recalling 3,664 Ilestro 7 VR-T DX implantable defibrillators due to a potential for premature battery depletion.
Stryker Spine is recalling 169 sets of Tritanium X TL instruments because non-conforming components could lead to device failure during surgery.
Biotronik is recalling Inventa 7 ICDs and CRT-Ds due to a potential for premature battery depletion. The recall covers devices distributed nationwide and worldwide.
Pacific Medical Group is recalling 2,452 aftermarket Alaris infusion pump front bezels installed between July 2020 and February 2021. The bezel posts may crack or separate, potentially causing infusion errors.
Hyundai is recalling 2013-2015 Santa Fe Sport vehicles because brake fluid may leak inside the ABS module, creating a risk of engine compartment fire.
Smiths Medical ASD Inc. is recalling specific lots of Medex High Pressure Adaptors and LogiCal Kits due to insufficient or incomplete welds.
Teligent Pharma is recalling 3,432 tubes of Flurandrenolide Ointment 0.05% because the product failed impurity and degradation specifications.
Smiths Medical ASD Inc. is recalling specific lots of LogiCal Left Heart Kits and related components due to insufficient or incomplete welds.
Biotronik is recalling 323 Ilestro 7 VR-T defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
BIOTRONIK is recalling 490 Iforia 7 implantable defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Trinity Sterile, Inc. is recalling 2,970 Midline Catheter Dressing Change Kits with Statlock because evidence of foreign material in the seal caused improper sealing and compromised sterility.
Biotronik Inc is recalling 285 Inventa 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.