State
72,968 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 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Evenflo is recalling Gold Revolve360 Slim and Revolve360 Slim child seats because loose headrest foam can break off and pose a choking hazard to children.
Land Rover is recalling certain 2023 Range Rover Evoque vehicles because water may enter the rearview camera, so the image may not appear on the display or may appear distorted.
General Motors is recalling certain 2024 Chevrolet Equinox EV vehicles because the pedestrian alert sound system may not change volume enough between standstill and low speed, failing FMVSS 141.
International Motors is recalling 2026 IC Bus CESB school buses because a weld failure may prevent the left-side wiper from working, increasing crash risk.
Altec is recalling 2021-2025 aerial devices because the outrigger pad holder may be installed too close to the exhaust, increasing fire risk.
International is recalling 2026 IC Bus CECB commercial buses because a weld on the wiper crank shaft may fail, causing the left-side wiper to stop working.
Kia is recalling certain 2021-2023 Sorento vehicles because the heating, ventilation and air conditioning blower motor wiring harness may be inadequate, which can result in a fire.
About 550 Autoez bamboo shades are recalled because long operating cords and accessible inner cords pose strangulation and entanglement hazards to children. No incidents reported.
3M Ranger Blood/Fluid Warming High Flow Sets are the subject of a field action to clarify flow rates, inlet fluid temperatures and the location of the outlet temperature. The FDA classified it as Class I.
Unichem Cyclobenzaprine Hydrochloride Tablets, 10 mg, lot GMML24026A, are recalled because bottles labeled as cyclobenzaprine contained yellow Meloxicam 7.5 mg tablets. The FDA classified the action as Class I.
SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCK, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 15,834 units are affected.
SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCMC, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 8,413 units are affected.
SmartDrive MX2+ SpeedControl Dials are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. The FDA classified the action as Class I. 25,389 units are affected.
Volkswagen is recalling certain 2025-2026 GTI, Golf R, Audi A5, S5, A6 and Q4 e-Tron models because the torsion bar in one or both front seat belt retractors may have been damaged during production.
Volkswagen is recalling one Audi SQ7 vehicle because the fasteners securing the high pressure fuel pump may not be tightened properly, resulting in a fuel leak. The vehicle has been repaired.
SureStep Foley Tray Systems with Bard Lubri-Sil catheters, REF A942216 lot NGJX4320, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating. 3,670 units are affected.
Fagron Sterile Services bevacizumab (Avastin) Injection, 1.25 mg/0.05 mL single-dose syringes, is recalled nationwide for lack of assurance of sterility. 109,320 syringes are affected.
Charge-Up Chilaquiles, 3.5 oz, lot 52061, is recalled because Yellow #5 and Yellow #6 are undeclared. 566 packages are affected.
Sun Pharmaceutical's Kit for the Preparation of Technetium Tc 99m Mertiatide, lot AD70995, is recalled after an out-of-specification result for sulphate in the sodium tartrate dihydrate used in production. 1,870 kits are affected.
Exactech Equinoxe Reverse Shoulder humeral liners in 38 mm and 42 mm sizes are recalled because the articular surface position falls outside the dimensional specification in the labeling. 11,542 units are affected.
Best Yet, Arctic Shores and Great American branded frozen cooked shrimp is recalled because it was made under insanitary conditions and may have been contaminated with Cesium-137. 11,081 cases are affected.
Exactech Equinoxe Reverse Shoulder humeral liners under REF 320-38 and 320-42 are recalled because the articular surface position falls outside the dimensional specification in the labeling. 61,334 units are affected.
SureStep Foley Tray Systems, REF A303414A lot NGJY3685, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating, risking infection or allergic reaction.
Sand Bar, Great American and First Street branded frozen raw shrimp in 2 pound bags is recalled because it was made under insanitary conditions and may have been contaminated with Cesium-137.
UniCel DxH 600 Coulter Cellular Analysis Systems configured with the LED HGB photometer are recalled because they may produce erroneously high hemoglobin results on samples with elevated white blood cell counts.