State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2020 Explorer and Lincoln Aviator vehicles because a missing parking brake cover or Factory Mode setting may allow the vehicle to roll away or hide gear selection.
Harley-Davidson is recalling specific Touring and CVO Touring motorcycles because a luggage conversion kit removed rear red reflectors without providing replacements, reducing visibility.
Forest River is recalling 2019-2020 Arctic Wolf and Flagstaff trailers because incorrect pin box bolts may allow the hitch to rotate, increasing crash risk.
Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because an improper weld on the fuel filler pipe may cause a fuel leak, increasing fire risk.
Mercedes-Benz is recalling certain 2018-2019 SL models because the front passenger air bag seam may tear during deployment, increasing injury risk.
Toyota is recalling 2019 Camry vehicles because the occupant classification system may be improperly calibrated, potentially preventing front passenger air bags from deploying in a crash.
Honda is recalling 2019 CR-V vehicles because an insufficient weld on the fuel tank may cause fuel leaks, increasing the risk of fire.
Winnebago is recalling 2018-2019 Fuse motorhomes because wheel studs may be too long, preventing lug nuts from securing wheels properly and increasing crash risk.
Thor Motor Coach is recalling 2019-2020 Omni and Magnitude motorhomes because the battery tray may detach, causing the vehicle to stall.
Super Jumper is recalling approximately 23,000 trampolines because welds on the metal railings can fail, posing fall and injury hazards.
Probar LLC is recalling 14,999 bars of PROBAR MEAL Original Trail Mix because they may contain undeclared milk and soy allergens.
Dorel Juvenile Group is recalling about 24,000 inclined infant sleepers, including Eddie Bauer and Disney Baby models, due to safety concerns about inclined sleep products.
The Crystal Spoon Corp. is recalling Top Chef Meals Grilled Bison Burgers due to potential E. coli contamination. Consumers should not eat the product.
Probar LLC is recalling 50,951 Chocolate Coconut meal bars because they may contain undeclared milk and soy allergens.
Probar LLC is recalling 61,849 Peanut Butter Chocolate Chip meal bars because they may contain undeclared milk and soy.
Pharma-Natural Inc. is recalling Workvie Instant Pain Relieving Roll On due to current good manufacturing practice deviations, including lack of process and cleaning validation.
Gordon Laboratories is recalling 277 boxes of MONSEL'S (Ferric Subsulfate) Solution due to microbial contamination and high iron content.
Tris Pharma is recalling 2,550 bottles of Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-Release Suspension due to high out-of-specification results for active ingredients and preservatives.
Geritrex, LLC is recalling 6,165 bottles of Gericare Diocto Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.
The FDA is recalling PROBAR Meal Wholeberry Blast bars because they may contain undeclared milk and soy ingredients. Consumers should discard affected bars and consult their healthcare provider if allergic.
Geritrex, LLC is recalling Ritussin DM Double Strength cough syrup due to cGMP deviations that may result in microbial contamination.
BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because improperly welded front seatback frames may fold unexpectedly, increasing injury risk in a crash.
Geritrex, LLC is recalling Preferred Plus Pharmacy Iron Elixir due to cGMP deviations that may result in microbial contamination.
Geritrex, LLC is recalling 5,107 bottles of Ritussin DM Children & Adults due to cGMP deviations that may result in microbial contamination.
Geritrex, LLC is recalling Preferred Plus Dioctyl Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.