State
73,824 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,823 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 1,494 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Brenner is recalling 2015-2017 Liquid Tank trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Moritz is recalling 2015-2016 trailers because axle mounting brackets may not be properly tightened, creating a risk of axle detachment and crashes.
Vermeer is recalling 2015-2016 TR620 and TR626 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Heartland is recalling 2015-2016 Revolution trailers because a rear gate brace blocks the rear clearance light, reducing visibility and increasing crash risk.
Chrysler is recalling 2017 Pacifica vehicles because a center overhead seat belt stow clip may fracture, preventing seat belt use and increasing injury risk in a crash.
Thor Motor Coach is recalling 2017 Outlaw motorhomes because a warning label near the fuel fill station is missing, which could increase the risk of fire if an operator smokes.
NatureBox is recalling Country Ranch Sunflower Kernels due to a supplier notification regarding Listeria monocytogenes. The product was sold nationwide online.
NatureBox is recalling Cheddar and Onion Sunflower Kernels due to a supplier notification regarding Listeria Monocytogenes contamination.
NatureBox, Inc. is recalling SunOpta Country Ranch Sunflower Kernels due to a supplier notification regarding Listeria Monocytogenes contamination.
Let's Talk Health is recalling 75 units of Tox Elim Liquid due to undeclared whey protein and soy lecithin, posing a risk to individuals with milk or soy allergies.
Let's Talk Health, Inc. is recalling Energizer Drink Mix Citrus because it contains undeclared whey protein (milk) and soy lecithin.
Let's Talk Health, Inc. is recalling specific lots of Pomegranate Energizer Drink Mix due to undeclared whey protein, which contains milk and soy lecithin.
Transcraft is recalling 2015-2017 Platform Trailers because improperly machined spring brake valves may delay braking, causing the trailer to roll away.
Let's Talk Health is recalling 200 units of Agua Vitae Kids Multi-Vitamin Liquid due to undeclared whey protein and soy lecithin.
Let's Talk Health, Inc. is recalling Aqua Vitae Multi-Vitamin due to undeclared whey protein and soy lecithin.
Let's Talk Health, Inc. is recalling specific lots of Energizer Drink Mix because they contain undeclared milk and soy.
Ford is recalling 2016 Transit Connect vehicles because metallic debris in the brake pump may degrade electronic stability control, increasing crash risk.
Wabash National is recalling 2015-2017 Van Trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Bickel's Snack Foods is recalling Golden Gourmet Veggie Chips because ranch-flavored chips containing milk were packed in plain bags.
Nissan is recalling 1,522 model year 2016 Sentra vehicles because an engine room harness terminal pin may be too large, potentially causing the engine to stall or fail to start.
Newmar is recalling 2017 Ventana and Dutch Star motorhomes because wipers may block the view or headlights may turn off, increasing crash risk.
Ceg Enterprises is recalling Germ Terminator GT100 toothbrush sanitizers due to reports of excessive heat, power cord discoloration, and suspected counterfeit UL labels.
Saro Trading is recalling about 7,800 children's nightgowns because they fail to meet federal flammability standards, posing a risk of burn injuries.
Immuno-Mycologics, Inc. is recalling 467 units of Histoplasma Yeast Complement Fixation Antigen Dilute (Lot 111WH3) due to bacterial contamination. The product was distributed nationwide to specific states.
Siemens Medical Solutions is recalling 2 Biograph TruePoint scanner upgrades because using non-Siemens phantoms for calibration may result in unexpected SUV values.