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.
Kubota is recalling about 3,850 zero turn mowers because the throttle cable can contact internal wiring, posing a fire hazard. No injuries have been reported.
Osage is recalling 2015-2019 Brave, Warrior, and Super Warrior ambulances because brake lights may illuminate when the brake pedal is not pressed, potentially confusing other drivers.
American Honda is recalling approximately 200,000 portable generators because a fuel valve leak can cause fire and burn hazards. No injuries have been reported.
Reckitt Benckiser is recalling Durex Pleasure Pack condoms because five batches failed burst pressure specifications.
Nature's Path is recalling Organic Chocolate Choco Chimps cereal because it may contain undeclared gluten (wheat and barley).
Volkswagen is recalling 2019 Atlas and 2020 Passat vehicles because incorrect side air bags may have been installed, potentially failing to deploy in a crash.
Reckitt Benckiser LLC is recalling Durex Real Feel condoms because five batches failed burst pressure specifications.
Thor Motor Coach is recalling 2018-2019 Quantum RW28 motorhomes because they may be missing mid-ship marker lights, which can cause other drivers to underestimate the vehicle's length.
Steris Corporation is recalling 68 AMSCO 5000 Series Washer/Disinfector units because a software defect may prevent the intended cleaning cycle from processing, potentially leading to inadequate disinfection.
Nature's Path is recalling Organic Gorilla Munch Corn Puffs cereal because it may contain undeclared gluten (wheat and barley). The recall covers 23,969 cases distributed nationwide and internationally.
Fouts Bros is recalling 2017-2018 F-3000, F-Rescue, and F-Pumper fire apparatus vehicles because brake lights may illuminate without the brake pedal being pressed.
Nature's Path is recalling Organic Cinnamon Jungle Munch cereal because it may contain undeclared gluten (wheat and barley).
US Endoscopy Group Inc is recalling Padlock Clip defect closure systems due to a risk of esophageal laceration during patient procedures.
Steris Corporation is recalling 11 AMSCO 3000 Series Washer/Disinfector units because a software defect may prevent intended processing cycles, risking inadequate cleaning or damage to medical instruments.
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz Sprinter and Metris vehicles because they left the plant without final quality inspection of safety-relevant parts.
Linet Spol. S.r.o. is recalling 253 AVE 2 Birthing Beds because the power cable may break or fail, posing a risk of sparks or exposure to live conductors.
Olympus is recalling two TJF-Q180V duodenoscopes because the adhesive used in their repair was incorrectly prepared, potentially affecting the device's durability or effectiveness.
Olympus is recalling two video colonoscopes because the adhesive used in their repair was incorrectly prepared, potentially affecting the durability of the repair.
Lannett Company Inc. is recalling 14,448 bottles of Oxybutynin Chloride Extended-Release Tablets because they failed to meet dissolution specifications.
Olympus is recalling one GIF-H180J videoscope because the adhesive used for its repair was incorrectly prepared, potentially affecting the device's durability.
Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed content uniformity specifications for blend uniformity.
Medtech Products is recalling 4,716 Little Remedies New Baby Essentials Kits because the cartons contain incorrect labeling for two of the five items inside.
Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed blend uniformity specifications. The recall covers 140,589 bottles distributed nationwide.
Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed blend uniformity specifications.
Zimmer Trabecular Metal Technology is recalling 24 units of NexGen Tibial Half Block Augments because the product in the box may not match the label.