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.
Lumber Liquidators is recalling 5-gallon mixing buckets because they lack required warning labels, posing a drowning risk to young children.
Öhlins is recalling about 5,400 front air suspension bicycle forks sold on Specialized bikes because the air cartridge can spring out, posing fall and injury risks.
Ducati is recalling 2,742 motorcycles because the shift knob may detach, preventing gear shifting and increasing crash risk.
Fujian Wanda is recalling aftermarket replacement windshields for 2014-2018 Toyota Highlanders because water leaks into the wire harness, potentially damaging the Engine Control Module and causing the engine to stall.
Mercedes-Benz is recalling specific 2018-2019 C-Class and GLC-Class vehicles because the passenger air bag status may display incorrectly, potentially leaving occupants unaware the air bag is off.
Airstream is recalling 2019 Interstate motorhomes because incorrect fuses may allow battery cables to overheat, increasing fire risk.
BMW is recalling one 2019 F850GS motorcycle because engine connecting rods may be loose, risking engine damage and loss of power.
Maserati is recalling 2014-2015 Quattroporte and Ghibli vehicles because damaged fuel lines may leak, increasing the risk of a fire.
Irvine Shade & Door is recalling windshield motor shades that may unroll while driving, potentially blocking the driver's view and increasing crash risk.
Volkswagen is recalling 2018-2019 Atlas, Tiguan, and Jetta vehicles because the instrument cluster may fail to provide an audible warning when the key is left in the ignition.
Nova Bus is recalling 2013-2018 LFS Artic transit buses because a software fault may cause the vehicle to operate at zero velocity and lack dampening, increasing crash risk.
FCA US LLC is recalling 2017-2018 Alfa Romeo Giulia AWD vehicles because brake fluid may leak onto the exhaust, increasing fire risk.
Chunwei, Inc. is recalling meat and poultry products because they are misbranded and may contain undeclared allergens and MSG, with no confirmed illness reports.
New Flyer is recalling certain 2013-2017 buses because a fire extinguisher actuator may fail, preventing the suppression system from discharging during a fire.
Epic Products, LLC is recalling Euphoric Premium Male Performance Enhancer capsules because they contain undeclared sildenafil, tadalafil, and oxytetracycline.
Sandoz Inc. is recalling 1,550 bottles of Isosorbide Dinitrate Tablets 20 mg due to cross-contamination with other products.
Zero Xtreme USA is recalling 16 bottles of Zero Xtreme Dietary Supplement capsules because they contain undeclared sibutramine and were marketed without an approved NDA or ANDA.
GE Healthcare is recalling 1,166 Millennium MG gamma camera systems because a detector can detach and fall.
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
GE Healthcare is recalling 4,207 Aisys anesthesia system touchscreen display kits because they fail to transition to backup ventilation if a patient stops breathing.
GE Healthcare is recalling 18 Millennium MC units because a detector can detach and fall.
Navistar is recalling certain 2018-2019 International trucks because a clutch component may fail, causing unintended vehicle movement and increasing crash risk.
Sandoz Inc. is recalling Isosorbide Dinitrate Tablets 5 mg due to cross-contamination with other products. The recall affects 7,817 bottles distributed nationwide.
Sandoz Inc. is recalling 5,100 bottles of Isosorbide Dinitrate Tablets, USP 10 mg, due to cross contamination with other products.
GE Healthcare is recalling 276 Millennium MyoSIGHT Nuclear Cardiology Imaging Systems because a detector can detach and fall.