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.
Newmar is recalling 2018-2019 motorhomes because improperly adjusted door latch rods may allow the entry door to open during transit.
Star Natural Meats is recalling raw pork sausage products because they contain undeclared milk, soy, and restricted ingredients.
Mercedes-Benz is recalling 2018 E 400 Cabrio vehicles because the child seat anchoring system may not be properly installed, increasing injury risk in a crash.
Freedman Seating Company is recalling GO-ES Foldaway Seats because the cushion may not stay locked during a crash, increasing injury risk.
Mercedes-Benz is recalling 2018 CLA250 and CLA45 AMG vehicles because the front passenger air bag may fail to deactivate if a child seat is installed.
Mercedes-Benz is recalling 2018 E-Class and 2019 CLS vehicles because the front passenger air bag may not deactivate if a child seat is installed, increasing injury risk.
Honda is recalling Genuine Accessory Centerstand Kits for 2016-2018 Africa Twin motorcycles because a broken circlip can cause the stand to detach, creating a road hazard or causing the bike to fall.
Mercedes-Benz is recalling 2018 GLE 350 and AMG GLE43 vehicles because the panoramic sunroof may not be properly adhered, creating a road hazard.
Van Oriental Foods Inc. is recalling pork egg rolls that may contain soft plastic. No illnesses have been reported.
Rena Ware is recalling about 700 Nutrex pressure cookers because they can discharge steam at lower pressures than intended, posing a burn hazard.
Zebra Technologies is expanding a recall of power supply units for thermal printers due to a fire hazard. The units can overheat and catch fire when exposed to moisture.
Dexter Axle Company is recalling certain trailer axles because incorrect tapered roller bearings may have been installed, increasing the risk of a crash.
Newmar is recalling 119 motorhomes because brake caliper mounting bolts may be insufficiently tightened, potentially reducing braking performance and increasing crash risk.
Subaru is recalling 2019 Ascent vehicles because missing spot welds on the B-Pillar may compromise vehicle strength, increasing the risk of injury in a crash.
Thor Motor Coach is recalling 2017-2019 Aria and Venetian motorhomes because brake caliper mounting bolts may loosen, potentially reducing braking performance.
Miller Fireworks is recalling specific rocket and cracker fireworks that violate federal standards due to explosion and burn hazards.
General Motors is recalling 2018 Chevrolet Express and GMC Savana vans because the tire pressure monitoring system may be incorrectly calibrated, potentially delaying low-pressure warnings.
CPSC recalls Hill Topper electric bike motor controllers that may accelerate on their own, posing crash and injury risks to riders.
Textron Specialized Vehicles is recalling about 255 Arctic Cat snowmobiles because the handgrip can break, posing an injury hazard to the rider.
Major Pharmaceuticals is recalling specific lots of 80 mg Valsartan tablets because a carcinogen impurity was detected in the active ingredient.
Olympus is recalling 2,399 Uretero-reno fiberscopes because the insertion tube bending section may break during surgery.
Major Pharmaceuticals is recalling specific lots of 160 mg Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Cayenne Medical Inc. is recalling specific models of the AperFix Femoral Implant Coring Removal Drill due to a trend of premature wear and breakage identified in 2010.
Philips Healthcare is recalling 459 Allura Xper systems because shutter positions reset when procedure types change, potentially affecting imaging accuracy.
Olympus is recalling 2,548 Uretero-reno videoscopes because the insertion tube bending section may break during surgery.