State
73,741 recalls have nationwide distribution and so reach South Carolina. 7,152 additional recalls listed South Carolina specifically in their distribution scope.
Of the 7,152 recalls naming South Carolina we have scored against our rubric, 1,275 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,169 (30%) are Severe.
Which agencies issued them
These figures cover only the 7,152 recalls whose distribution notice names South Carolina specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling 2017-2019 Fiat 124 Spider vehicles with automatic transmissions due to a software defect that may cause unexpected downshifting and sudden deceleration.
Indian Motorcycle is recalling Scout and Scout Bobber models because an accessory brake lever may apply the front brake unintentionally, increasing crash risk.
Fisher-Price is recalling about 44,000 Children's Power Wheels Barbie Dream Campers because the vehicles can continue running after the foot pedal is released.
DeWALT is recalling DWD110 and DWD112 drills because internal wiring can contact moving parts, posing a shock hazard. No injuries have been reported.
Mazda is recalling 2016-2019 MX-5 vehicles with automatic transmissions because incorrect software may cause unexpected downshifting and abrupt deceleration.
Forest River is recalling 2019 Rockwood and Flagstaff trailers because improper wiring may prevent brakes from engaging if the trailer disconnects from the tow vehicle.
Ford is recalling 2019 Ranger vehicles with 10-speed automatic transmissions because the shift lever can move from Park without the key or brake pedal, risking unexpected movement.
Daimler Vans is recalling 2019 Mercedes-Benz Sprinter VS30 vehicles because the steering shaft may disconnect, causing a sudden loss of steering control.
Life Line Emergency Vehicles is recalling 2017-2019 Type I and Type III ambulances because Whelen accessory brake lights may falsely illuminate, potentially confusing other drivers.
Draeger Medical is recalling 170 units of VentStar Basic 250 breathing circuits because they were incorrectly pre-assembled, creating a risk of incorrect connection or short circuiting.
Draeger Medical is recalling 325 units of VentStar Basic 180 breathing circuits due to incorrect pre-assembly that may cause incorrect connections.
Draeger Medical is recalling 525 units of VentStar Basic (P) 180 breathing circuits because they were incorrectly pre-assembled, posing a risk of incorrect connection or short circuiting.
Bound Tree Medical is recalling Epi Safe Administration and Training Kits because the instructions recommend an unapproved epinephrine dosage for young children.
Bound Tree Medical is recalling 339 Curaplex Epi Kits because the instructions recommend an unapproved epinephrine dosage for young children.
Draeger Medical is recalling 25 units of VentStar Watertrap (P) 180 breathing circuits because they were incorrectly pre-assembled, posing a risk of incorrect connection.
Teleflex Medical is recalling Percuvance Percutaneous Shafts because the distal tip may deform or break off during use, potentially compromising the tool's security.
Del Monte is recalling Fiesta Corn seasoned with Red & Green Peppers because incorrect thermal processing may allow Clostridium botulinum growth.
Teleflex Medical is recalling 1,962 units of Percuvance Percutaneous Shafts because the distal tip may deform or break off during use, potentially requiring surgical intervention.
Draeger Medical is recalling 25 units of ID Circuit Watertrap breathing circuits because they were incorrectly pre-assembled, creating a risk of incorrect connection or short circuit.
Proterra is recalling 2015-2018 Catalyst buses because a height control system may overload front tires, increasing crash risk.
Draeger Medical is recalling 25 units of ID Circuit Basic 180 breathing circuits due to incorrect pre-assembly that may cause connection errors.
Draeger Medical is recalling 20 units of ID Circuit Basic 250 breathing circuits due to incorrect pre-assembly that may cause connection errors.
Dr. Reddy's is recalling specific bottles of Ezetimibe and Simvastatin tablets because black speckles were observed on the tablets.
Draeger Medical is recalling 75 units of VentStar Basic (P) 250 breathing circuits because they were incorrectly pre-assembled, creating a risk of incorrect connection or short circuit.
Draeger Medical is recalling 10 units of VentStar Anesthesia WT(P) 180 breathing circuits due to incorrect pre-assembly that could cause incorrect connections.