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.
Forest River is recalling specific model years of Auto Plus, Sandpiper, Vengeance, Cargo Mate, Hydra-Lift, and XLR trailers because wheel studs may break, potentially causing the wheel to detach.
Performance Machine is recalling certain Coastal Moto Phantom motorcycle wheels because spokes may crack, potentially impairing vehicle handling and increasing crash risk.
Spartan Motors is recalling 144 model year 2015-2016 K2, K3, and MM chassis because rear axle fasteners may be loose, risking loss of vehicle control.
Champion is recalling 2013-2015 transit buses because seat belts may rub against metal frames and fray, failing federal safety standards.
Nuevotanicals is recalling Greenjoy Herbal Mind & Body Shots because the product contains Kratom. The recall covers products distributed in twelve states.
Jaguar Land Rover is recalling 2012-2013 LR4 vehicles because the panoramic roof adhesive may not secure the assembly, increasing crash risk.
Jaguar Land Rover is recalling 2013-2016 Range Rover and 2014-2016 Range Rover Sport vehicles because doors may unlatch unexpectedly, increasing crash risk.
Philips Medical Systems is recalling Extended Brilliance Workstation UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Baxter Healthcare is recalling specific lots of Heparin Sodium in Sodium Chloride Injection because the raw material was found to be subpotent and out of specification.
ResMed is recalling Astral 100 and 150 ventilators because clinicians can disable all alarms, including circuit disconnection alerts, posing a risk of insufficient ventilation.
Akorn, Inc. is recalling Hydroxyzine Hydrochloride oral solution because it failed impurities and degradation specifications. The product was distributed nationwide, including Puerto Rico.
Nuevotanicals is recalling Kr8om Max3 and Kr8om Max10 capsules because they contain Kratom. The products were distributed in 12 states.
Smith & Nephew is recalling 40 units of R3 Constrained Liners because the locking groove is oversized, preventing the locking ring from engaging properly.
Nuevotanicals is recalling Kratom alkaloid suspension oil products because they contain Kratom.
Fresenius Medical Care is recalling CRIT-LINE Blood Chambers because the connection may leak during use.
Philips Medical Systems is recalling 23 Ingenuity Flex UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Philips Medical Systems is recalling Precedence 6 UPS accessory devices for CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Zimmer is voluntarily recalling 752 M/L Taper hip implants because they contain higher than allowed cytotoxicity levels, posing a risk of adverse biological response.
Philips is recalling 15 Gemini GXL 16 Slice CT systems worldwide because their UPS accessory devices may leak battery acid, overheat, or emit fumes.
Roche Diabetes Care is recalling Accu-Chek Spirit insulin pumps because mechanical errors may stop insulin delivery, potentially leading to severe hyperglycemia.
Transportation Collaborative, Inc. is recalling 2012-2015 Trans Tech Student Safety Transport buses because the rear axle may fail if loaded to full capacity.
Smith & Nephew is recalling R3 Constrained Liners because the locking groove is oversized, which may prevent the locking ring from engaging properly.
Roche is recalling Accu-Chek Spirit Combo insulin pumps because mechanical errors may stop insulin delivery, potentially leading to severe hyperglycemia.
Philips is recalling 31 TruFlight Select PET/CT systems because the Uninterruptible Power Supply (UPS) accessory devices may leak battery acid, overheat, or emit fumes.
HeartWare Inc is recalling HVAD systems due to complaints of damaged or bent connection pins in the power supply ports of the VAD controller.