State
73,741 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,822 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,493 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mercedes-Benz is recalling 2018 AMG E63S vehicles because the front passenger seat may adjust beyond its intended limit, increasing injury risk in a crash.
Ford is recalling 120V convenience charge cords for 2012-2015 C-Max, Fusion, and Focus Electric vehicles because they lack thermistors, creating a fire risk.
Turtle Top is recalling 2013-2018 Odyssey, VanTerra, and Terra Transit buses because a wheelchair lift cam may fail, allowing the platform to rise too high.
Trailstar is recalling 2019 Dump trailers because improperly installed wheel end nuts may cause the wheel to separate from the axle, increasing crash risk.
REV Ambulance Group is recalling 2017-2018 ambulances equipped with Whelen accessory brake lights that may illuminate without the brake pedal being pressed.
General Motors is recalling 2014-2016 Cadillac CTS vehicles because damaged front seat heaters may overheat and cause a fire when the car is remotely started.
Navistar is recalling 2019 IC Bus CE and RE school buses because a parking brake component may be improperly crimped, causing air leaks and increased stopping distances.
Navistar is recalling 2,089 2019 International and IC Bus vehicles because a brake chamber defect may cause air leaks, increasing stopping distance and crash risk.
Honda is recalling 793 2017 Acura NSX vehicles because road vibrations may loosen screws, causing the center brake light to fail and increasing crash risk.
Nissan is recalling specific 2015-2018 Murano, Maxima, Pathfinder, and 2017 QX60 vehicles because brake fluid leaks may cause electrical shorts and fires.
Honda is recalling 2017-2018 Acura NSX vehicles because fuel tank couplers may leak, increasing the risk of fire if an ignition source is present.
General Motors is recalling 2015 Chevrolet, GMC, and Cadillac vehicles because electric power steering assist may momentarily be lost and then suddenly return, increasing crash risk.
Halcore Group is recalling 2017-2018 AEV Traumahawk ambulances because Whelen accessory brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Micro Bird is recalling 252 2018 MB II school buses because certain child restraint seats are missing warning labels, which may lead to improper use and injury.
Lester Electrical is recalling about 19,000 Links Series golf cart chargers because the control board can fail and overheat, posing fire and burn hazards.
Nissan is recalling 2019 Infiniti QX50 vehicles because the passenger-side knee air bag cover may separate unexpectedly in cold crashes, increasing injury risk.
TJX is recalling swivel barstools sold at HomeGoods, Marshalls, and T.J. Maxx because wood joints can break, posing a fall hazard. Three minor injuries have been reported.
Auro Pharmacies is recalling 81 vials of Methyl-Cobalamin injectable because processes and equipment were inadequate to assure sterility.
Haemonetics is recalling 348 OrthoPAT QuickConnect Reservoirs because a missing cannula prevents blood from being emptied and processed.
Torrent Pharma Inc. is recalling specific batches of Amlodipine, Valsartan, and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Torrent Pharma Inc. is recalling specific batches of Amlodipine and Valsartan Tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Fabform is recalling 2017-2018 Power Tilt dump trailers because welded hinges may fracture, causing the dump box to fall unexpectedly and increasing the risk of injury or death.
Pharmcore Inc. is recalling 5,718 vials of Human Chorionic Gonadotropin 5000 IU due to a lack of assurance of sterility.
Auro Pharmacies is recalling 43 vials of Testosterone Cypionate/Enanthate injectable because inadequate processes and equipment failed to assure product sterility.
Auro Pharmacies is recalling 39 vials of CoEnzyme-Q10 injectable because inadequate processes and equipment failed to assure product sterility.