State
72,940 recalls have nationwide distribution and so reach Oklahoma. 5,788 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,788 recalls naming Oklahoma we have scored against our rubric, 1,033 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,238 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,788 recalls whose distribution notice names Oklahoma specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Securitas Healthcare is recalling 1,898 Arial 900 MHz Call Stations, model CSK200-900MR, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.
IMRIS Imaging is recalling 122 HFD100 Head Fixation Devices because a torque screw may crack or separate, which could lead to inadequate head stabilization and risk of patient injury.
Remote Diagnostic Technologies is recalling 7,129 Philips Tempus Pro Patient Monitors because intracranial and bladder pressure measurements have not been tested or validated for accuracy.
Securitas Healthcare is recalling 5,627 Arial 900 MHz Call Stations, model CSK200-900, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.
Beckman Coulter is recalling 6,457 UniCel DxI 800 analyzers because a potential communication issue may prevent the instrument restarting after a standard shutdown, causing delayed results.
Alembic Pharmaceuticals is recalling Fesoterodine Fumarate Extended-release Tablets, 8 mg, because levels of a diester impurity exceeded the specification limit.
Integra LifeSciences is recalling 1,301 Codman Microsensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.
AvKARE is recalling 7,991 cartons of Rosuvastatin Tablets, USP 10 mg, because the product was out of specification for dissolution.
Sophysa is recalling 105 Pressio 2 ICP Monitoring Systems following customer complaints of the Pressio monitor rebooting.
SpecGx is recalling 287,988 bottles of Oxycodone and Acetaminophen CII Tablets, 10 mg/325 mg, because of the potential for the imprint to be missing on tablets.
Beckman Coulter is recalling 1,272 UniCel DxI 600 analyzers because a potential communication issue may prevent the instrument restarting after a standard shutdown, causing delayed results.
Integra LifeSciences is recalling 5,116 Codman CereLink ICP Sensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.
SpecGx is recalling 74,544 bottles of Oxycodone and Acetaminophen CII Tablets, 7.5 mg/325 mg, because of the potential for the imprint to be missing on tablets.
Ziyad Brothers Importing is recalling 2,865 cases of Baraka French Style Puff Pastry because the product may contain partially hydrogenated oils.
Ziyad Brothers Importing is recalling 575 cases of Baraka Gourmet Pastry Kunafe because the product may contain partially hydrogenated oils.
East Trailers is recalling 2024-2026 Beast and Beast II trailers because an improper weld may cause the rear impact guard to detach, increasing crash injury risk.
Lippert is recalling 3000 Series Hidden Hinge Ramp Doors because they may break away from the frame during use, increasing the risk of injury.
Terex is recalling 2025 TL, LT, LTM40, HR40, HR46, and SCM55 aerial devices because a control valve defect may cause hydraulic equipment to overheat, posing a burn risk.
Jaguar Land Rover is recalling 2026 Range Rover Sport vehicles because the certification label lists incorrect weight information, which could lead to overloading.
Goodyear is recalling specific Cooper Discoverer SRX tires because incorrect Tire Identification Numbers prevent proper registration and compliance with federal safety standards.
About 18,700 Julie and Judah pajama and lounge pants and shorts are being recalled because they violate the mandatory flammability standards for children's sleepwear.
About 1,430 NFSVLB baby bath seats are being recalled because they are unstable, can tip over, and have leg openings that allow a child's torso to become entrapped.
About 4,155 Vasicar 18-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 870 Rattan 6-Drawer Dressers, model YD001, are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 60,250 DR Power walk-behind and tow-behind leaf vacuums are being recalled because pieces can come loose inside the unit or debris can pierce the chute, ejecting material.