State
72,940 recalls have nationwide distribution and so reach North Carolina. 10,261 additional recalls listed North Carolina specifically in their distribution scope.
Of the 10,261 recalls naming North Carolina we have scored against our rubric, 1,476 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,520 (25%) are Severe.
Which agencies issued them
These figures cover only the 10,261 recalls whose distribution notice names North Carolina specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Aju Pharm is recalling 2,569 AlternatiV+ Max Knotless Anchors after reports of device failure including anchor breakage, bending, pull out and suture breakage.
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.
Gold Star Distribution is recalling toothbrushes and toothpaste-with-brush packs over potential exposure of rodents and rodent activity in its distribution center.
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.
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.
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.
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.
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.
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.
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.
Philips North America is recalling 5 units of the Ingenia Elition S because exported MR Elastography stiffness maps may show stiffness value errors.
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.
Gold Star Distribution is recalling first aid kits and bandages over potential exposure of rodents and rodent activity in its distribution center.
Cardinal Health is updating the instructions for use on 1,169,726 chest drainage units to clarify that the intended patient population is adults 18 years and older.
Philips North America is recalling 1 unit of the SmartPath to dStream for 3.0T 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.
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.
Weaver's Brew is recalling 1,014 cases of Goldenroot Lemon Ginger Hibiscus Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.
Gold Star Distribution is recalling pregnancy tests over potential exposure of rodents and rodent activity in its distribution center.
Philips North America is recalling 3 units of the Evolution Upgrade 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Aju Pharm is recalling 1,088 units of the Fixone Biocomposite Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
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 21 units of the Ingenia Ambition X because exported MR Elastography stiffness maps may show stiffness value errors.