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.
ADM is recalling Baker's Corner All Purpose Flour because of the potential presence of E. coli O26. The product was sold at ALDI stores in 11 states.
ADM is recalling specific lots of flour products due to the potential presence of E. coli O26. The affected products were distributed to retailers and commercial bakeries in multiple states.
ADM is recalling Pillsbury Hi Gluten Flour because of potential E. coli O26 contamination. The affected flour was distributed to food service in New York and Pennsylvania.
Datascope Corp. is recalling CS100 Intra-Aortic Balloon Pumps because improper battery maintenance may result in less than minimum run time. Revised labeling and training are being offered.
Datascope Corp. is recalling 6,197 Cardiosave Hybrid Intra-Aortic Balloon Pumps worldwide due to inadequate labeling regarding battery maintenance.
ADM is recalling bulk flour products due to the potential presence of E. coli O26. The affected flour was distributed to retailers and commercial bakeries in multiple states.
Chang Type is recalling Porter-Cable 10-inch table saws sold at Lowe's because the motors can overheat and cause fires. No injuries have been reported.
Daimler Trucks North America is recalling 2019-2020 Freightliner Cascadia trucks because brake airlines may be damaged, reducing brake effectiveness and increasing crash risk.
Datascope Corp. is recalling CS300 Intra-Aortic Balloon Pumps because improper battery maintenance may result in less than the minimum required operating power.
ADM is recalling specific lots of Latina Niagra Flour due to the potential presence of E. coli O26. Consumers should check their pantry for the affected product code and lot number.
Braun is recalling 2016-2019 Ford Explorer BraunAbility MXV wheelchair accessible vehicles because an electric solenoid may overheat, causing a fire.
ADM is recalling specific lots of Dominator Flour because of the potential presence of E. coli O26. The product was distributed in New York and Pennsylvania.
ADM is recalling various flour products, including King Arthur and Pillsbury brands, due to the potential presence of E. coli O26.
Olympus is recalling WM-NP2 and WM-DP2 mobile workstations because the control panel arm may cause the unit to fall over if a heavy monitor is attached.
DeRoyal is recalling 108 custom surgical packs in Oklahoma because they contain defective Cardinal Health Blunt Cannulas that could compromise sterility.
Sprouts Farmers Market is recalling 1,046 cases of Cut Leaf Spinach because testing revealed the presence of Listeria monocytogenes.
Trek is recalling Kickster balance bikes because the steer tube clamp can break, posing a fall hazard to children. Consumers should take bikes to a retailer for a free repair.
GE Healthcare is recalling Revolution CT scanners because they may expose patients to additional low-dose radiation.
DJO, LLC is recalling 9 units of Aircast REF 3011 sterile cuffs because they may not meet sterility requirements.
Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vehicles because the printed operator's manual may not match the vehicle's features, increasing crash risk.
Oregon Potato Company is recalling 2,970 cases of frozen whole red raspberries due to potential Norovirus contamination. The product was distributed across ten western and central US states.
Daimler Trucks North America is recalling specific Thomas Built Buses because the roof escape hatch handle may break, preventing emergency exit.
Zimmer Biomet is recalling 92 Comprehensive Reverse Shoulder Instrument Cases because they lack adequate sterilization validation. The products were distributed in the US and 16 foreign countries.
Zimmer Biomet is recalling 1,257 Comprehensive Reverse Shoulder Instrument Cases because they lack adequate sterilization validation. The products were distributed in the US and 16 foreign countries.
Clariance Inc is recalling Erisma-LP posterior fixation system components due to a potential for polyaxial screws to disassemble during implantation.