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.
Gillig LLC is recalling specific fire extinguishers sold as aftermarket parts because the actuator may fail to discharge the suppression agent, increasing injury risk during a fire.
Kubota is recalling approximately 11,670 zero turn mowers because the rollover protective structure can loosen and fail to protect the operator during a rollover accident.
Penn State Industries is recalling about 1,000 quick change jaw chuck systems for woodworking lathes because the jaws can loosen and break off, posing a laceration hazard.
Daimler Trucks North America is recalling 2017-2019 Thomas Built Buses Saf-T-Liner C2 school buses because improperly applied roof adhesive may reduce roof header strength during a rollover crash.
Daimler Trucks North America is recalling 2017-2019 Thomas Built Buses Saf-T-Liner C2 transit buses because improperly applied roof adhesive may increase injury risk in rollover crashes.
Forest River is recalling 2019 Rockport vehicles because the Federal Placard may display an incorrect Gross Axle Weight Rating, potentially allowing the vehicle to be overloaded.
PACCAR is recalling 2018 Kenworth and Peterbilt trucks because seat belt buckles may be glued instead of sewn, risking separation in a crash.
Mercedes-Benz is recalling two 2018 vehicles because the steering coupling may not be locked, which could reduce steering ability and increase crash risk.
Micro Bird is recalling 2015-2018 CT-Series buses because foldaway seats may not stay locked during a crash, increasing injury risk.
Rosenbauer America is recalling 2017-2018 Fire Apparatus vehicles because Whelen accessory brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Altec is recalling 2017-2018 Aerial Devices, Service Bodies, and Digger Derricks because Whelen accessory brake lights may illuminate without the brake pedal being pressed.
Keystone RV Company is recalling 2018-2019 Raptor recreational trailers because an incorrectly routed propane line allows the grill to be stored while lit, increasing fire risk.
Kawasaki is recalling 1,173 2018 Z900 and Z900RS motorcycles because the rear brake hose or sensor wire may contact the tire, risking brake failure or ABS malfunction.
Kawasaki is recalling about 1,000 Mule Pro off-highway utility vehicles because the rollover protection structure may fail to protect occupants, posing an injury hazard.
Meijer is recalling about 25,000 Falls Creek Kids infant and toddler hoodies because the zipper slider can detach, posing a choking hazard to young children.
Skip Hop is recalling Tuo convertible high chairs because the legs can detach from the seat, posing fall and injury hazards to children.
General Motors is recalling 2019 Chevrolet Silverado 1500 and GMC Sierra 1500 Crew Cab vehicles because the passenger-side air bag may not inflate properly in a crash.
NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.
Volkswagen is recalling 2018 Golf R vehicles because a fuel hose connector may detach, causing a leak that increases fire risk.
Eurotrol Inc. is recalling HemoTrol Level 2 hematology quality control mixtures because microbial contamination causes incorrect measurement results.
NxStage Medical is recalling 7,275 units of PureFlow B Solution because the bag's smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.
Synaptive Medical Inc is recalling 37 units of BrightMatter Guide software due to a defect that occurs when switching between specific port trajectories during surgery.
Volkswagen is recalling 2015-2016 Audi A6 and 2015 A7 vehicles because an incorrectly inserted auxiliary heater connector may overheat and cause a fire.
Maquet Cardiovascular is recalling QUADROX-i Neonatal membrane oxygenators due to a potential for blood leakage at the blood inlet connector when using a specific reducing screw adapter.
NxStage Medical is recalling specific lots of PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.