State
73,566 recalls have nationwide distribution and so reach North Carolina. 10,299 additional recalls listed North Carolina specifically in their distribution scope.
Of the 10,299 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 2,899 (28%) are Severe.
Which agencies issued them
These figures cover only the 10,299 recalls whose distribution notice names North Carolina specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2022 F-150 and related models due to a software error that may disable trailer brake functionality. Loss of trailer brakes increases stopping distance and crash risk.
Boxine US is recalling tonies Blocks wooden toys containing high-powered magnets sold online from November through December 2021. When swallowed, multiple magnets can lodge in the digestive system and cause serious injury or death.
Prevost is recalling 140 X3-45 Commuter buses from 2021-2022 because a loose cable in the rear junction box may overheat and cause a fire.
EGL Motor is recalling about 500 EGL and ACE-branded youth ATVs (models MADIX 110 and B125) sold nationwide from May to September 2020 due to violations of federal ATV safety standards. The vehicles exceed speed limits for their age group, have defective brakes, and handlebars that pose laceration hazards in crashes.
Chrysler is recalling 2021-2022 Pacifica and 2021 Voyager vehicles because the second-row seat mounting latch may fail to secure the seat properly, increasing the risk of injury in a crash.
Commencal Ramones 14-inch children's bicycles lack required foot brakes and are equipped only with hand brakes, posing a crash hazard or risk of injury to young children unable to stop them. About 925 bicycles are affected.
Segway is recalling about 960 Ninebot children's bicycle helmets because they fail to meet safety standards for positional stability and retention, creating a risk of head injury in a crash. No injuries have been reported.
Sakar International is recalling about 89,000 Dimensions Bluetooth Speaker Helmets sold at Walmart because they do not meet U.S. federal safety standards for bicycle helmets and pose a risk of head injury in a fall.
Reading Truck is recalling 2019-2021 Master Mechanic Crane vehicles because a poorly mounted module can overheat and cause a fire.
Certain 2021-2022 Jeep Grand Cherokee L vehicles may have a missing weld in the child seat tether anchorage system. This could allow the tether to separate during a crash, increasing the risk of child injury.
Family Pharmacy of Statesville is recalling Trimix (Alprostadil/Papaverine/Phentolamine) injectable vials distributed in North Carolina due to lack of assurance of sterility.
Audi is recalling 2013-2017 A8, S6, S7, S8, and RS7 vehicles because a blocked turbocharger oil strainer can cause engine failure and increase crash risk.
Volkswagen is recalling certain 2022 and 2021 vehicles because rear suspension knuckles may corrode, crack, and break, potentially causing loss of stability and increasing crash risk.
Family Pharmacy of Statesville is recalling one lot of Fentanyl 150 mcg/mL Infusion Solution in 250 mL bags because the manufacturer cannot assure the product's sterility.
B. Braun Medical, Inc. is recalling 33,742 bags of 0.9% Sodium Chloride Injection USP due to leaking that compromises sterility assurance. The intravenous medication was distributed nationwide.
Jaguar Power Honey packaged in gold boxes is being recalled nationwide because it contains a hidden drug ingredient not listed on the label. Consumers should not consume this product.
SD Biosensor's STANDARD Q COVID-19 Ag Home Test kits were illegally imported without FDA approval, clearance, or authorization. Approximately 400,000 units were distributed nationwide.
Family Pharmacy of Statesville is recalling three bags of Ketamine 50 mg Infusion Solution because the manufacturer cannot assure sterility of the product.
Walmart is recalling Avaphinal Maximum Male Enhancement Sexual Pills (2000 MG, 10-capsule cartons, Lot DK1027) distributed nationwide because they contain undeclared sildenafil, making them an unapproved drug.
Family Pharmacy of Statesville is recalling Hydromorphone HCl 5 mg/mL Infusion in 250 mL bags because the manufacturer cannot assure the product meets sterility requirements.
Family Pharmacy of Statesville is recalling Morphine Sulfate 6 mg/mL infusions in 250 mL bags due to lack of assurance of sterility. The affected product was distributed in North Carolina.
Ice cream products manufactured by Royal Ice Cream Company in Manchester, CT are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed across multiple states under various retail and food service brand names.
Family Pharmacy of Statesville is recalling Vancomycin 14 mg/mL Fortified Ophthalmic Solution due to lack of assurance of sterility. The affected lot was distributed in North Carolina.
Family Pharmacy of Statesville is recalling four bags of Hydromorphone HCl 1 mg/mL (250 mL each) distributed in North Carolina due to lack of assurance of sterility. The affected lots have beyond-use dates of October 25–30, 2020.
Family Pharmacy of Statesville is recalling Hydromorphone HCl 2 mg/mL Infusion 250 mL bags (2 units) distributed in North Carolina due to lack of assurance of sterility.