State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hickory Springs is recalling specific school bus seats because the foam in the knee impact area may not absorb enough energy in a crash, increasing injury risk.
BMW is recalling 2018 M5 vehicles because a fuel level sensor may stick to a fuel line, causing inaccurate fuel gauge readings that could lead to stalling and increased crash risk.
Ford is recalling 2013-2016 Fusion and 2013-2014 Escape vehicles because a transmission shifter cable bushing may degrade, allowing the vehicle to move unexpectedly.
TRW is recalling brake caliper pistons with insufficient coating for vehicles from Volkswagen, Fiat Chrysler, BMW, and Mercedes-Benz to prevent reduced braking performance.
Ford is recalling 2018 F53 stripped chassis vehicles because improperly heat-treated front wheel studs may break, increasing crash risk.
Keystone RV Company is recalling 2018-2019 Dutchmen Aerolite trailers because the safety chains are rated lower than the trailer's weight, increasing crash risk if detached.
Volkswagen is recalling 2018 Tiguan vehicles because the panoramic sunroof LED module may short circuit, increasing the risk of a fire.
Forest River is recalling 2019 Palomino hardside truck campers because the Federal Placard lists an incorrect dry weight, which may result in the vehicle being overloaded.
Chrysler is recalling specific 2014-2018 Chrysler 300, Dodge Charger, and Challenger vehicles because a defect may prevent the cruise control system from disengaging.
Allura Imports is recalling about 64,000 children's pajamas and onesies because they fail to meet federal flammability standards, posing a burn risk.
Multiquip is recalling 2018 TRLR45H and TRLR70USH trailers because the center-mounted jack may collapse under excessive load, increasing the risk of injury.
FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter may damage implanted leads if over-tightened, potentially requiring replacement.
FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter can damage implanted leads and stylets when over-tightened, requiring device replacement.
FHC, Inc. is recalling the microTargeting STar Drive System (Manual) because the Depth Stop Adapter may damage the lead and stylet if the screw is over-tightened.
FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter can damage leads and stylets, potentially causing short circuits.
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads, causing short circuits and requiring replacement.
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads and stylets, requiring replacement.
FHC, Inc. is recalling Depth Stop Adapters because over-tightening the screw can damage implanted leads, requiring removal and replacement.
FHC, Inc. is recalling the microTargeting Drive System Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring replacement.
Ingenus Pharmaceuticals is recalling Irinotecan Hydrochloride Injection because of high out-of-specification assay values for potency.
Fagron Compounding Services is recalling 390 prefilled syringes of Neostigmine Methylsulfate Injection Solution because some may be incorrectly labeled with the wrong strength.
Fagron Sterile Services is recalling 840 prefilled syringes of Neostigmine Methylsulfate Injection Solution because they may be incorrectly labeled with the wrong strength.
FHC, Inc. is recalling 2,952 microTargeting Drive Systems because over-tightening the depth stop screw can damage implanted leads, requiring replacement.
Howmedica Osteonics Corp. is recalling specific LFIT Anatomic CoCr Femoral Heads because of a higher than expected number of complaints regarding disassociation from the hip stem.
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring surgical replacement.