State
73,809 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,823 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 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Honda is recalling 2,443 2017 CBR1000RR and CBR1000RR SP motorcycles because a gap in the fuel tank cap seal may allow water to enter the tank, potentially causing engine stalling and increasing crash risk.
Jaguar Land Rover is recalling 2017 Range Rover and Range Rover Sport vehicles because the instrument cluster may intermittently go blank, increasing crash risk.
Jaguar is recalling 2016-2018 XF, F-Pace, XJ, and XE vehicles because the instrument cluster may go blank, increasing crash risk.
The Harvard Drug Group is recalling Alprazolam Tablets, 0.25 mg, due to an out-of-specification result for an unknown impurity.
Keystone is recalling 2017-2018 Cougar western edition trailers because stabilizer jacks may detach during transit, creating a road hazard.
BMW is recalling 2006-2011 3 Series vehicles because heating and air conditioning wiring may overheat, increasing the risk of a fire.
Death Wish Coffee Company is recalling 80,777 cans of Nitro Canned Cold Brew Coffee nationwide due to a potential for Clostridium Botulinum.
St. Jude Medical is recalling 1,744 Proclaim DRG Implantable Pulse Generators because the battery indicator status may be inaccurate.
St. Jude Medical is recalling 3,119 Infinity 5 and 7 Implantable Pulse Generators because battery longevity estimations may be inaccurate.
Volkswagen Group of America is recalling 2017-2018 Audi A4 and A5 vehicles because loose aluminum door trim can expose sharp edges, increasing the risk of injury to occupants.
St. Jude Medical is recalling 28,817 Proclaim 5 and 7 Elite Implantable Pulse Generators because battery longevity estimations may be inaccurate.
Diving Unlimited International is recalling approximately 480 scuba diving regulators because they can malfunction, posing a drowning hazard. No injuries have been reported.
CareFusion 303, Inc. is recalling Alaris Pump Module model 8100 units due to reports of increased or decreased medication flows.
Bel Brands USA is recalling Merkts Port Wine Cheese Spread after customers reported finding white plastic pieces in the product.
PlanToys is recalling about 500 baby gyms sold in 2016 and 2017 because babies can strangle on the side rope crossbars. No injuries have been reported.
Medtronic is recalling 423 VCLAS laser applicator systems because they were not appropriately tested for saline leakage during manufacturing.
Unichem Pharmaceuticals is recalling 96,876 bottles of Bisoprolol Fumarate 5 mg tablets because stability testing revealed an out-of-specification unknown impurity.
Philips is recalling Brilliance iCT SP CT systems because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patients to be rescanned.
Philips Electronics North America Corporation is recalling 606 Brilliance 64 CT systems in the US because a software defect prevents image reconstruction after certain scans.
Philips is recalling 606 Ingenuity Core CT systems in the US because a software defect prevents image reconstruction after bolus tracking scans.
Teleflex Medical is recalling Pilling Knife Handles because the slot depth is out of specification, which may prevent blades from fitting properly.
Philips is recalling Brilliance iCT CT scanners because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patients to be rescanned.
Toshiba American Medical Systems Inc is recalling 96 Kalare Fluoroscopic X-Ray Systems because images may fail to display on the system monitor or save to the hard disk.
Philips is recalling Ingenuity Core128 CT systems because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patient rescans.
Philips is recalling Ingenuity CT systems because a software defect prevents image generation during bolus tracking procedures, potentially requiring patient rescans.