State
72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Aston Martin is recalling 2024 Valkyrie vehicles because incorrect screws may damage the wiring harness, potentially causing loss of critical functions and increasing crash risk.
Chrysler is recalling specific Mopar side curtain air bags because improperly sealed seams may cause insufficient pressure retention, increasing the risk of ejection and injury during a crash.
Chrysler is recalling certain Ram 2500 and 3500 vehicles with a 3.5 inch cluster and column shifter because a software error may make the gear selection display inaccurate.
General Motors is recalling 2025 Chevrolet Express and GMC Savana vehicles because the front passenger seat head restraint may be improperly welded, increasing injury risk in a crash.
Chrysler is recalling certain 2022-2025 Pacifica and Voyager vehicles because improperly sealed seams may leave the side curtain airbags with insufficient pressure retention.
Chrysler is recalling certain 2019-2024 Ram 1500 vehicles because the driver's side airbag may not be connected properly, which can prevent deployment. 71 units affected.
DEMDACO is recalling approximately 3,000 Maril Brand 8-ounce scented candles because the glass container can crack or break while burning, posing laceration and fire hazards. Three incidents of glass breaking have been reported, with no injuries or property damage so far.
Legend Brands is recalling approximately 500 Bliss hair dryers due to lack of immersion protection, which can cause death or serious injury from electrocution if the dryers fall into water while plugged in. No injuries have been reported.
Yamaha Corporation of America is recalling about 37,400 PA-300C AC power adaptors that can overheat and ignite. The company has received four reports of adaptors burning or smoking, though no injuries have been reported.
Delta-branded Gas Ball Valves pose fire and burn hazards because small amounts of gas can leak from the valve when it is in the open position. About 3,700 units were sold in the United States.
Sanven Technology recalls approximately 800 Vevor stainless steel cable railing kits sold online from May 2021 through September 2024 because the bottom hole on the cable support posts poses an entrapment hazard to children.
Volvo is recalling certain 2021-2025 vehicles because the rearview camera image may not display when the vehicle is placed in reverse. 413,151 units are affected.
About 3,400 Xylolin peg doll toy sets sold on Amazon.com are being recalled because the spherical ends of the peg dolls can block a child's airway, posing a choking risk. Consumers should take the product away from children immediately and dispose of it.
Thor Motor Coach is recalling 2025-2026 Outlaw motorhomes because step bracket bolts may loosen, allowing steps to detach and increase injury risk.
Deuter USA is recalling Kid Comfort, Kid Comfort Pro, and Kid Comfort Active Child Carriers because hinges on the foldable rear kickstand support leg can crack or break, creating a fall hazard. No injuries have been reported.
Certain GE Healthcare CARESTATION 750 A2 anesthesia systems may not provide effective ventilation in Volume Control Ventilation mode. Users should switch to Pressure Control Ventilation or Manual ventilation modes.
GE Healthcare CARESTATION 650C A1 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Ventilation can be achieved using alternate modes or manual ventilation.
Waldemar Link GmbH & Co. KG is recalling Distal Femoral Augment devices because the preassembled femoral augment screw was missing its thread. The defect may affect proper device function.
GE Healthcare CARESTATION 620 A1 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Effective ventilation is available in Pressure Control or Manual ventilation modes.
GE Healthcare CARESTATION 750c A1 anesthesia systems may not provide effective ventilation in Volume Control Ventilation mode. Affected units can achieve ventilation through alternative modes or manual operation.
Waldemar Link is recalling Posterior Femoral Augments used in knee surgery because some units were delivered with a preassembled screw missing its thread, which could compromise surgical fixation.
Waldemar Link GmbH & Co. KG is recalling Tibial Augment devices distributed nationwide because preassembled Femoral Augment screws were delivered missing their threads.
American Regent, Inc. is recalling certain lots of Nicardipine Hydrochloride Injection due to product leakage around the vial neck that could compromise sterility assurance. The recall affects 7,249 cartons distributed nationwide.
American Regent, Inc. is recalling Nicardipine Hydrochloride Injection due to product leakage around the vial neck that could compromise sterility assurance. The recall affects multiple lots distributed nationwide.
Certain GE Healthcare CARESTATION 620, 650, 650c, 750, and 750c anesthesia delivery systems may not provide effective ventilation in Volume Control Ventilation (VCV) mode. Effective ventilation is available using other ventilation modes or manual ventilation.