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.
Datascope is recalling the CS300 IABP running software version C.01 because the battery runtime and cycle specifications in the device's Instructions for Use need to be updated.
Acme United Corporation is recalling Dukal BZK Antiseptic Towelettes over current good manufacturing practice deviations.
Acme United Corporation is recalling Green Guard Antiseptic Wipes over current good manufacturing practice deviations.
Cipla USA is recalling three lots of Nilotinib Capsules 150 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.
Cipla USA is recalling one lot of Nilotinib Capsules 200 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.
Mercedes-Benz is recalling 2026 GLA 250 vehicles because an incorrectly installed bowden cable may prevent the door from opening from inside, potentially trapping occupants.
Kia is recalling certain 2026 K4 vehicles because the rear center seat belt anchor buckle may not latch properly, risking occupant restraint failure in a crash.
Webasto is recalling specific CV Standard Gen1 traction batteries that may fail, potentially causing loss of drive power or a fire.
Forest River is recalling 2026 Dynamax Europa and Grand Sport GT motorhomes because the distribution panel may not be properly bonded to the chassis ground, posing a risk of injury or electrocution.
Toyota is recalling certain 2021-2024 Highlander and Highlander Hybrid vehicles because the second-row seat backs may fail to lock into position during seat back adjustment.
GM is recalling certain 2025-2026 Chevrolet Silverado 3500 and GMC Sierra 3500 vehicles with gasoline engines and dual fuel tanks because the rear fuel pump may not transfer adequate fuel to the front tank.
Forest River is recalling 2026 Impression fifth wheel trailers because exposed wire conductors may cause electrical arcing and increase fire risk.
Pebble Mobility is recalling 2026 Flow recreational trailers because the adhesive securing roof solar panels may fail, creating a road hazard.
General Motors is recalling 2025-2026 Chevrolet Express and GMC Savana cutaway vehicles because tires may have sidewall damage, increasing crash risk.
Forever 21 Kids Disney Mickey Mouse Pajama Pants are being recalled because they violate the mandatory flammability standards for children's sleepwear.
Tomum Minoxidil Hair Growth Treatment spray bottles are being recalled because the bottles are not child-resistant, as required for minoxidil under the Poison Prevention Packaging Act.
HALO Magic Sleepsuits in three batch codes are being recalled because the zipper head can detach from the garment, posing a choking hazard to infants.
Escape Trailer Industries is recalling 2025 E17, E19, E21, and E5.0 recreational trailers because the spare tire carrier may detach during transit, creating a road hazard.
Cubimana Island Storm 3 In 1 Building Sets are being recalled because the battery compartment in the LED light piece lets children access button cell batteries.
Mitsubishi Fuso is recalling 2024-2025 Rizon trucks because an electrical control unit error may prevent the vehicle from moving, increasing crash risk.
Prime Food Processing is recalling Dried Croaker Fish, 8 oz, because the fish is uneviscerated. The FDA has classified this recall as Class I, its most serious category.
Agebox is recalling 665 bottles of iKids-Growth Day Formula capsules because they contain undeclared ibutamoren, a drug ingredient not approved for marketing in the U.S.
Olympus is recalling all lots of its Inner Sheath, Model A2641, used in urological endoscopic procedures, due to complaints that the ceramic tip can break during use.
Encore Medical, LP is recalling 20 Reverse Shoulder Prosthesis implants due to incorrect labeling. The recall affects nationwide distribution across multiple US states.
Wizcure Pharmaa is recalling all lots of Fluorescein Sodium Ophthalmic Strips because the products may not have been manufactured according to current good manufacturing practices, raising concerns about sterility assurance.