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.
Greenstone is recalling 3,456 cartons of methylprednisolone tablets Dosepak, 4 mg, because the blister foil was applied in the wrong orientation, giving incorrect dosing information.
Philips North America is recalling 24 units of the Ingenia 3.0T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Siemens is recalling 41 units of the LUMINOS Q.namix R fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.
Gold Star Distribution is recalling condoms over potential exposure of rodents and rodent activity in its distribution center.
Philips North America is recalling 6 units of the Ingenia 3.0T CX MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Daimler Coaches is recalling 2026 Mercedes-Benz Tourrider buses because a faulty door valve may prevent doors from opening, delaying emergency evacuation.
About 700 Scepter B62 gas and oil combination fuel containers are being recalled because they lack flame mitigation devices and the spout is not child-resistant.
Gold Star Distribution is recalling feminine hygiene products over potential exposure of rodents and rodent activity in its distribution center.
Aju Pharm is recalling 400 units of the Genesis Dual Thread Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Gold Star Distribution is recalling first aid kits and bandages over potential exposure of rodents and rodent activity in its distribution center.
Philips North America is recalling 3 units of the SmartPath to dStream for XR and 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.
Philips North America is recalling 5 units of the Ingenia Elition S because exported MR Elastography stiffness maps may show stiffness value errors.
Aju Pharm is recalling 600 units of the Genesis Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Aju Pharm is recalling 2,569 AlternatiV+ Max Knotless Anchors after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Weaver's Brew is recalling 421 cases of Goldenroot Lemon Ginger Jalapeno Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.
Quten Research Institute is recalling Qunol Extra Strength Turmeric 1000mg capsules after mold contamination was detected in raw material lots produced in July and used in finished goods.
Philips North America is recalling 9 units of the MR 7700 MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Philips North America is recalling 31 units of the Ingenia Elition X MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Philips North America is recalling 1 unit of the Evolution Upgrade 3.0T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Prima Vera Nueva is recalling 16,790 packages (4 tamales per package) of Black Bean Bonanza Tamales with Black Beans over potential contamination with Listeria monocytogenes.
LSL Healthcare is recalling 1,400 Central Line Dressing Kits because the BD ChloraPrep Triple Swabsticks inside exhibit an open seal on the applicator packaging.
NIPRO Technical Services is recalling 499 units of Conductivity Standard Solution because a defect in the solution can cause meters to report incorrect conductivity values for dialysate.
Philips North America is recalling 10 units of the Ingenia 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Siemens is recalling 7 units of the LUMINOS Q.namix T fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.
Aju Pharm is recalling 233 units of the Fixone Hybrid Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.