State
73,596 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, 1,311 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,049 (24%) are Severe.
Which agencies issued them
These figures cover only the 8,391 recalls whose distribution notice names Arizona specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling 2021 Cadillac Escalade vehicles because the front passenger seat belt and airbag status lights may be invisible in daytime, increasing crash injury risk.
Shilpa Medicare Limited is voluntarily recalling 2,064 vials of Busulfan Injection due to CGMP deviations. The recall is nationwide and the lot expired in December 2020.
Volkswagen Group of America is recalling 2020 Audi Q3 vehicles because the brake pedal plate can bend or detach, increasing crash risk.
LG Energy Solution Michigan is recalling about 1,815 RESU 10H home batteries because they can overheat and cause fires. Consumers should contact the company for a free replacement.
Shilpa Medicare Limited is voluntarily recalling 35,931 vials of Azacitidine for Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Fresenius Kabi is recalling 13,525 bottles of Dexmedetomidine HCl Injection due to cross-contamination with trace amounts of lidocaine.
Volkswagen is recalling 2012-2014 Beetle and Beetle Convertible vehicles because the driver's side air bag inflator may explode due to propellant degradation.
Shilpa Medicare Limited is recalling 2,008 vials of Docetaxel Injection USP due to Current Good Manufacturing Practice (CGMP) deviations.
Shilpa Medicare Limited is recalling 4,166 bottles of Imatinib Mesylate 400 mg tablets nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Daimler Trucks North America is recalling 28 electric school buses where the parking brake may release unexpectedly, increasing crash risk.
Shilpa Medicare Limited is recalling 6,560 vials of Azacitidine for Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall is voluntary and nationwide.
JMH International is recalling Chef Myron's Premium Teriyaki Sauce because it contains wheat-derived gluten despite a gluten-free claim.
Camp Chef is recalling about 20,600 portable gas stoves because a sharp edge on an internal gas regulator part can cause gas leaks, posing a fire hazard.
Medtronic is recalling 71,030 Evolut PRO System units worldwide due to a potential for transcatheter aortic valve leaflet damage during post-implant balloon dilatation.
Mani, Inc. is recalling Trocar Kit 23G S units because Luer connector dimensions are out of specification, which may cause fluid leakage or disconnection during ophthalmic surgery.
Kroger is recalling HomeChef Pretzel-Crusted Chicken meal kits because a supplier ingredient was suspect for Listeria species.
Graco is recalling inclined sleeper accessories for four playard models due to a risk of infant suffocation. Consumers should stop using the accessory immediately and contact Graco for a refund.
Philips is recalling 16 IntelliVue X2 Multi Measurement Servers because speaker failures may prevent audible alarms, potentially delaying patient treatment.
Shimadzu Medical Systems is recalling 22 MH-200S X-Ray systems because a software issue could cause the ceiling arm to move unexpectedly, posing a risk of collision or harm to patients and operators.
Medtronic is recalling Evolut R System transcatheter aortic valves due to a potential risk of leaflet damage during post-implant balloon dilatation.
K2M, Inc. is recalling 197 units of the Everest MI XT Tab Removal Tool because the threaded interface may crack, causing Loctite to leak from the handle.
JMH International is recalling Chef Myron's Szechuan Sauce because it contains wheat-derived fermented soy sauce despite a gluten-free claim.
Medtronic is recalling 19,961 Evolut PRO+ Transcatheter Aortic Valve systems due to a potential for leaflet damage during post-implant balloon dilatation.
Chromsystems Instruments & Chemicals GmbH is voluntarily recalling 342 vials of MassChrom Amino Acid Analysis Plasma Control Level III due to a Class II device defect.
Cycling Sports Group is recalling about 1,270 Cannondale Canvas NEO e-bicycles because the front fender can detach and stop the wheel, posing a fall hazard.