State
73,486 recalls have nationwide distribution and so reach North Carolina. 10,298 additional recalls listed North Carolina specifically in their distribution scope.
Of the 10,298 recalls naming North Carolina we have scored against our rubric, 1,486 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,898 (28%) are Severe.
Which agencies issued them
These figures cover only the 10,298 recalls whose distribution notice names North Carolina specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
RayStation 9B SP1 radiation treatment planning software has an issue where treatment course information may not be propagated to other systems in some workflows. This could potentially affect treatment planning accuracy.
Queen Bee Gardens recalls Truffle Dark Gift Box due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product poses a risk to consumers with tree nut allergies.
Honeymoons Dark Chocolate Cashew products may contain undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. The product is being recalled from Queen Bee retail locations in Colorado, New Mexico, Wyoming, and nationwide online.
Queen Bee Gardens is recalling Honeymoons Milk Chocolate Pecan candies due to the potential presence of undeclared tree nuts. Consumers with tree nut allergies should not consume this product.
Cipla is recalling 8,136 bottles of Difluprednate ophthalmic emulsion nationwide due to defective container caps that can break and expose the medication tip, compromising sterility.
Becton Dickinson is recalling approximately 1.96 million BD Connecta Stopcock devices due to potential leakage at the housing component, which could interrupt treatment and expose patients to biohazardous material.
Queen Bee Gardens is recalling Chocolate Sampler 13 oz packages due to undeclared tree nuts. The products may contain pecans, almonds, coconut, macadamia nuts, or walnuts.
Aesculap is recalling its S4 Cervical Cross Connector used in spinal fusion surgery due to insufficient clamping force that may cause the connectors to move on the rods or shed particles.
Queen Bee Gardens is recalling Macadamia Classic Truffles because they may contain undeclared tree nuts including almonds, coconut, and walnuts. The product poses allergen risks to consumers with tree nut allergies.
Nephron Sterile Compounding Center is recalling Oxytocin 30 Units/500 mL injectable solution due to lack of sterility assurance. Approximately 1,810 bags with lot codes OX2013C and OX2013E were distributed nationwide.
Certain 2022-2023 BMW IX and 2022 i4 vehicles are recalled due to high-voltage batteries that may develop internal damage and short-circuit, posing a fire risk. Owners should not drive or charge the vehicle until the battery is replaced.
Queen Bee Gardens is recalling Almond Coconut Classic Truffles for undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). The affected product was sold in Colorado, New Mexico, Wyoming, and nationwide online.
Nephron Sterile Compounding Center is recalling HYDROmorphone HCl Injection syringes nationwide due to lack of assurance of sterility. The recall affects 12,900 syringes across two manufacturing lots.
Queen Bee Gardens is recalling Dark on Dark Classic Truffle products due to the potential presence of undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, and walnuts) that pose an allergen risk to sensitive consumers.
Nephron Sterile Compounding Center is recalling 2,315 pre-filled syringes due to lack of sterility assurance. The compounded injectable medication was distributed nationwide.
Queen Bee Gardens is recalling QBee Sea Salt Caramel due to undeclared tree nuts. The affected product was sold at ten retail locations in Colorado, New Mexico, and Wyoming, and via internet sales.
Becton Dickinson is recalling BD Connecta Stopcocks due to potential leakage at the housing component. The defect may interrupt treatment and expose patients to biohazardous material.
Nephron Sterile Compounding Center recalls 36,354 pre-filled syringes of Sodium Bicarbonate Injection due to lack of sterility assurance. The medication was distributed nationwide.
Hill-Rom PRO+ mattresses are being recalled for a Microclimate Management feature failure that could increase pressure ulcer risk in patients. The recall affects 200 units distributed in the US and Canada.
Aesculap Implant Systems is recalling the AESCULAP S4 Cervical Cross Connector (product code SWT113T) used in spinal fusion surgery. The connectors may not clamp properly onto rods, potentially causing movement and wear particles.
The ENNOVATE MIS removal key used in spinal fixation systems may fracture if the 90-degree angle is not maintained during use. A product redesign is underway.
Stryker is recalling Triton Canister Scanning Labels that may have color variance issues, potentially resulting in lower-than-expected blood loss estimates. The recall affects 16,700 units distributed nationwide.
Nephron Sterile Compounding Center is recalling 18,840 syringes of Succinylcholine Chloride Injection nationwide because the manufacturing process cannot be assured to have maintained sterility.
Becton Dickinson recalls BD Connecta 3-Way Stopcocks due to potential leakage at the housing that may delay treatment and expose patients to biohazardous material.
Nephron Sterile Compounding Center is recalling Morphine Sulfate Injection syringes distributed nationwide due to lack of assurance of sterility. Approximately 43,385 syringes are affected.