State
73,833 recalls have nationwide distribution and so reach Oklahoma. 5,824 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,824 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 5,824 recalls whose distribution notice names Oklahoma specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The FDA is recalling OxiMax N-560 Pulse Oximeters because missing display segments may cause users to misinterpret oxygen saturation and pulse rate data.
FDA is recalling OxiMax N-65 handheld pulse oximeters because missing display segments may cause users to misinterpret oxygen saturation and pulse rate data.
Disney Store is recalling about 300 Gadget Pencil Cases because the magnets on the lids can detach and be swallowed, posing a serious internal injury risk to children.
Prism Medical is recalling 409 P-600 Portable Ceiling Lifts because sling loops may not stay attached to the carry bar hooks.
Prism Medical is recalling P-440 Portable Ceiling Lifts because sling loops may not stay attached to the carry bar hooks.
MZB is recalling about 1.9 million children's watches because the case-back can detach, exposing the interior to water and causing skin irritation or chemical burns.
Dairy Farmers of America is recalling specific fat-free Swiss cheese products because plastic film strips may remain attached to the slices.
Siemens is recalling ACUSON S 1000, S 2000, and S 3000 ultrasound systems due to a potential measurement error in the Doppler manual trace tool that could lead to misdiagnosis.
Philips is recalling 82 Ingenuity Core CT systems due to software errors affecting image quality, dose control, and heart rate monitoring.
Philips Medical Systems is recalling two Brilliance iCT SP CT systems due to software issues affecting image quality, dose control, and heart rate measurement.
Philips is recalling 38 Brilliance iCT CT systems due to software errors affecting dose control, heart rate measurement, and image artifacts.
Newmar is recalling 82 model year 2015-2016 Mountain Aire, King Aire, and Essex motor homes because the air suspension control module may lose power, potentially affecting vehicle control.
Philips is recalling 139 Ingenuity Core 128 CT scanners due to software errors affecting image quality, dose control, and heart rate monitoring.
Winnebago is recalling 2012-2016 Era recreational vehicles because certification labels list incorrect front tire inflation pressures, which could lead to tire failure.
Dairy Farmers of America is recalling specific Sandwich Mate cheese slices because a piece of plastic film might remain attached to the product.
Oxysure Systems is recalling 1,005 Model 615 oxygen cartridges because they do not meet FDA flow rate standards.
Ameritrans is recalling 2015 225 vehicles because the back-up camera may display reversed images, increasing the risk of a crash.
Boehringer Ingelheim is recalling 358,647 Combivent Respimat inhalers because the delivery system may fail to spray properly.
Dairy Farmers of America is recalling Borden Fat Free Sharp Cheddar cheese because a piece of plastic film strip might remain attached to the cheese slice.
Dairy Farmers of America is recalling Borden 2% Pepper Jack White cheese because plastic film strips may remain attached to the slices.
Siemens is recalling ACUSON S2000 and S3000 ultrasound systems with Virtual Touch IQ due to a potential measurement alignment error.
Dairy Farmers of America is recalling Meijer Monterey Pepper Jack cheese slices because a piece of plastic film might remain attached to the cheese.
Dairy Farmers of America is recalling specific Borden Sucrem and Country Fare imitation cheese slices because plastic film may remain attached to the product.
Dairy Farmers of America is recalling various brands of fat free American cheese because a piece of plastic film strip might remain attached to the cheese slice.
Dairy Farmers of America is recalling Borden Sensations Applewood Bacon Cheddar because a piece of plastic film might remain attached to the cheese slice.