State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pharmaceutical Associates, Inc. is recalling Nystatin Oral Suspension because it tested below the required potency level.
Organic By Nature, Inc. is recalling Nested Naturals Super Kids powder because the flaxseed ingredient contains an unapproved herbicide.
Randox Laboratories is recalling Chemistry QC Premium Plus due to incorrect Sodium target values. The error affects quality control accuracy for diagnostic assays.
Organic By Nature, Inc. is recalling Alkamind Creamy Vanilla Organic Daily Protein because the flaxseed powder ingredient contains unapproved herbicide Haloxyfop.
Siemens Healthcare Diagnostics is recalling Dimension Vista Total Bilirubin reagent cartridges because they may produce inaccurate results for patients taking eltrombopag.
Organic By Nature is recalling Slim Natural Raw Meal due to the presence of unapproved herbicide Haloxyfop in the flaxseed powder.
Siemens Healthcare Diagnostics is recalling Atellica CH Ethyl Alcohol assays due to potential positive bias in results within the 10-day calibration interval.
Organic By Nature is recalling RAWr! Life Organic Superfoods because the flaxseed powder ingredient contains an unapproved herbicide.
Quidel is recalling Triage TOX Drug Screen Control 1 kits due to a programming error in the control chip that causes false failing results for AMP and mAMP tests.
Organic By Nature, Inc. is recalling Alkamind Creamy Chocolate Organic Daily Protein due to the presence of unapproved herbicide Haloxyfop in the flaxseed powder ingredient.
Bard Peripheral Vascular Inc is recalling 178 PowerPort implantable ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgery.
Mylan Pharmaceuticals is recalling specific lots of 5mg Tacrolimus capsules because 1mg capsules may be present in the bottles.
Organic By Nature, Inc. is recalling Purim Daily Fiber Blend because the flaxseed ingredient contains unapproved herbicide Haloxyfop.
Grato Holdings, Inc. is recalling 659 bottles of Colostat homeopathic remedy because the indications on the product label are incorrect.
Cummins is recalling specific B6.7 diesel engines used in school buses, trucks, and emergency vehicles because the fuel heater may overheat, melt, or cause a fire.
Subaru is recalling 2019 Crosstrek vehicles because the rear seat belt locking mechanism may not function as intended, increasing injury risk in crashes.
Altec is recalling 2016-2018 AT200A vehicles because incorrect rear tire markings may cause overloading, increasing crash risk.
Nissan is recalling 216,678 vehicles from 2011-2017 because the driver-side air bag inflator may rupture during deployment, potentially causing serious injury or death.
Bombardier is recalling 2020 Can-Am Spyder RT motorcycles because a brake support could break during emergency braking, causing total loss of braking ability.
BMW is recalling 2013-2016 328d xDrive vehicles because a driveline joint may fail, causing loss of rear power and increasing crash risk.
Chrysler is recalling 2019 Jeep Grand Cherokee and Dodge Durango vehicles because insufficiently hardened front differential pinion gears can wear down, leading to a loss of power or the PARK function.
Land Rover is recalling 2020 Range Rover Evoque vehicles because some headliners lack a required metal plate, potentially reducing head impact protection in a crash.
Daimler Vans USA is recalling 2019 Sprinter vans because the Operator's Manual may contain incorrect information about the automatic parking function, potentially increasing crash risk.
General Motors is recalling 2019-2020 Chevrolet Bolt EVs because a rear door cable may be too long, potentially causing the door to open unintentionally while driving.
Philips is recalling HeartStart MRx Monitor/Defibrillators because internal damage from drops or shocks may prevent therapy delivery, even if the device appears undamaged.