State
73,817 recalls have nationwide distribution and so reach South Carolina. 7,153 additional recalls listed South Carolina specifically in their distribution scope.
Of the 7,153 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 2,170 (30%) are Severe.
Which agencies issued them
These figures cover only the 7,153 recalls whose distribution notice names South Carolina specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The Anspach Effort, Inc. is recalling 462 System Console units because the supplied directions for use did not contain a recommended service interval.
Profile Design is recalling Cobra S bicycle handlebar stems because they can corrode and break, causing riders to lose control and crash.
FCA US LLC is recalling 2013-2016 Ram 1500, 2500, and 3500 trucks because a sensor fault may disable side curtain air bags and seat belt pretensioners, increasing injury risk in crashes.
Mercedes-Benz is recalling 5,818 vehicles because electronic stability control software may keep brakes slightly applied, increasing crash and fire risks.
Chrysler is recalling 2017 Jeep Compass vehicles because the left front halfshaft may not be properly seated, potentially causing loss of drive or vehicle roll.
General Motors is recalling 2016-2017 Chevrolet Spark vehicles because the front passenger air bag may injure an unbelted child's neck during deployment.
The USDA FSIS issued a public health alert for frozen ready-to-eat fried chicken and pork sausage products due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Polaris is recalling about 6,000 model year 2017 RMK and SKS snowmobiles because a steering post weld can separate, causing loss of control.
Norgren Inc. is recalling one Kneeling Module because improperly seated snap rings may cause a loss of suspension air pressure, increasing crash and injury risks.
American Honda is recalling about 2,200 2017 Pioneer 700 recreational off-highway vehicles because a manufacturing defect may cause the front passenger seat belt buckle to fail.
Forest River is recalling 2017 XLR ToyHauler trailers because the Federal Placard incorrectly lists rear tire pressure as 50psi instead of 80psi, which could lead to tire failure.
TRW is recalling aftermarket lower ball joints for Toyota 4Runner, Sequoia, and Tundra vehicles because a design defect could cause steering loss and increase crash risk.
DGFA is recalling about 200 women's scarves sold on Amazon because they fail to meet federal flammability standards, posing a burn risk.
Springs Window Fashions is recalling motorized window coverings sold with Zeus brand lithium batteries due to fire and burn hazards.
Akron Brass Company is recalling Ultrajet firefighting nozzles because internal components may bind, limiting water output and hindering firefighting efforts.
Segway is recalling specific off-board chargers for Personal Transporters because a wire can detach and cause a shock hazard. No injuries have been reported.
KZRV is recalling 2018 Sport Trek and Durango travel trailers with outside kitchens due to potential propane line leaks that could cause fire or explosion.
Marcho Farms is recalling approximately 5,620 pounds of veal, beef, and pork products due to possible non-O157 Shiga toxin-producing E. coli contamination.
Combi USA is recalling about 1,000 Shuttle Travel Systems because the car seat can disengage from the stroller frame, posing a fall hazard to infants.
Honda is recalling 2015-2016 CR-Vs that received replacement engines potentially built with wrong pistons, which may cause engine stalls and increase crash risk.
Jim Reed's Truck Sales is recalling 2014-2016 Hino 338 trucks because certification labels fail to identify the final stage manufacturer, potentially hindering safety recall awareness.
Isomeric Pharmacy Solution, LLC is recalling 5,165 bottles of Phenylephrine 2.5% and Tropicamide 1% ophthalmic drops due to a lack of assurance of sterility.
Isomeric Pharmacy Solution, LLC is recalling 2,335 vials of Triamcinolone Acetonide and Lidocaine HCl injection due to production processes that cannot assure sterility.
The FDA is recalling hCG Body Shaper because it was marketed without approval and contains human chorionic gonadotropin, making it an unapproved drug.
Medtronic is notifying clinicians that an improved splice kit is available to replace the HeartWare HVAD Pump Driveline Splice Kit due to a safety issue.