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.
Oshkosh is recalling 2018-2019 S-Series Mixer vehicles because hydraulic hoses may be installed incorrectly, causing loss of steering assist and increasing crash risk.
Forest River is recalling 2019-2020 Georgetown and FR3 motorhomes because slide-out mechanisms may activate unintentionally, increasing injury risk.
Forest River is recalling 2017-2020 Shasta and Coachmen recreational trailers because exterior kitchen outlets may lack GFCI protection, posing an electrical shock risk.
Navistar is recalling 2011 IC Bus RE, CE, and BE school buses because plastic parts on non-retractable seat belt buckles may crack, making them difficult to fasten.
Ranee's is recalling about 55 women's beach cover-ups because they fail to meet federal flammability standards, posing a risk of burn injuries.
H.E. Industrial is recalling Profusion Heat electric garage heaters because the heating element can overheat, posing a fire hazard. No injuries have been reported in the United States.
Honeywell is recalling about 22,000 photoelectric smoke sensors sold with fire alarm systems because they may fail to alert occupants of a fire.
Forest River is recalling 2020 Work and Play fifthwheel trailers because generator cables may not be isolated, creating a risk of electrical short and fire.
Specialty Manufacturing is recalling Prolo 24-inch roof hatches because the external handle may break, preventing emergency exit from the vehicle.
Charles Machine is recalling 2018-2019 Ditch Witch trailers because improperly crimped brake wire terminals may cause the brakes to fail, increasing crash risk.
Navistar is recalling 2011 IC CE transit buses because plastic parts on the seat belt buckles may crack, preventing proper restraint in a crash.
TRW is recalling air bag electronic control units that may malfunction, potentially disabling or unexpectedly deploying air bags and seat belt pretensioners.
Hunter Fan Company is recalling Brunswick ceiling fans because damaged light kit wires pose an electric shock hazard. No injuries have been reported.
Heritage Pharmaceuticals is recalling Prochlorperazine Edisylate Injection because microbial growth was detected in a sublot. The affected vials are distributed nationwide.
Heritage Pharmaceuticals is recalling Amikacin Sulfate Injection vials because microbial growth was detected in a sub-lot. The affected product is distributed nationwide in the USA.
Blue Bird is recalling 2018-2019 Vision and All American electric school buses because a software defect may cause the vehicle to lose drive and power steering.
Pharm D Solutions is recalling specific lots of Trimix injectable vials due to a lack of sterility assurance.
Pharm D Solutions, LLC is recalling Sermorelin/GHRP-2 &6 vials due to a lack of sterility assurance. The recall affects products distributed nationwide in the United States.
Pharm D Solutions, LLC is recalling Sermorelin/GHRP-2 &6 vials nationwide because the product lacks sterility assurance.
Pharm D Solutions is recalling specific lots of Testosterone Cypionate 200 mg/mL vials due to a lack of sterility assurance.
Pharm D Solutions is recalling 100 vials of Sermorelin/GHRP-2 & 6 due to a lack of sterility assurance. The products were distributed nationwide in the United States.
Edwards Lifesciences is recalling IntraClude Intra-Aortic Occlusion Devices because the balloon may rupture during cardiopulmonary bypass, potentially obscuring the operative site and requiring a change in surgical strategy.
Pharm D Solutions is recalling Nandrolone Decanoate 200 mg/mL injectable vials due to a lack of sterility assurance. The recall covers 50 vials distributed nationwide.
Synthetopes Inc is recalling Sn-d, l-Exametazime vials nationwide due to a lack of processing controls. The FDA classifies this as a Class II recall.
Pharm D Solutions, LLC is recalling Sermorelin/GHRP-2 9 mg/9 mg vials because they may lack sterility assurance. The recall covers 6 vials distributed nationwide.