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.
Forest River is recalling 2017-2019 Crossfit coaches because incorrect weight placards may lead to vehicle overloading and increased crash risk.
Group Rossignol is recalling LOOK Pivot ski bindings because the heel piece can loosen, posing a fall hazard to skiers.
Newmar is recalling 2018 motorhomes because loose electrical connections in the breaker box may overheat and increase the risk of a fire.
KME is recalling 38 Predator fire trucks because improperly routed hydraulic hoses may contact electrical components, creating a fire risk.
Isuzu is recalling 2018-2019 NPR models because a brake switch retainer may not be secured, potentially disabling acceleration and increasing crash risk.
Chrysler is recalling 2018 Jeep Wrangler vehicles because the rear underbody ladder rail may corrode, potentially weakening the floor pan and loosening the rear seat mount.
Forest River is recalling 2018-2019 FR3 and Georgetown recreational vehicles because the entry door latch may not engage fully, allowing the door to open unexpectedly while moving.
General Motors is recalling 2018 Buick Regal vehicles because rear seat belts may be improperly routed, potentially failing to restrain passengers in a crash.
Forest River is recalling 2018 Salem recreational trailers because the federal placards list incorrect tire pressure, which may lead to under-inflation and increased crash risk.
L.L.Bean is recalling Allagash fixed blade hunting knives because the blade can cut through the leather sheath, posing a laceration hazard.
The King Arthur Flour Company is recalling 100% Organic Finely Ground Coconut Flour because it tested positive for Salmonella. Consumers should stop using the product.
Natural Grocers by Vitamin Cottage is recalling Organic Coconut Smiles because the product tested positive for Salmonella.
Volkswagen Group of America is recalling specific Audi models because a coolant pump defect may cause overheating or short-circuiting, increasing the risk of a fire.
Conagra Brands is recalling approximately 135,159 pounds of Salisbury steak products due to possible bone contamination. The recall follows reports of minor oral injuries.
International Harvest, Inc. is recalling Organic Go Smile! Dried Coconut Raw because the product tested positive for Salmonella.
GE Healthcare is recalling 1,742 units of the Monica Novii Wireless Patch System because incorrectly reconnected cables may cause fetal and maternal heart rate signals to be displayed swapped.
Fresenius Medical Care is recalling 127 K2 Hemodialysis Machines because a software defect may allow the ultrafiltration pump to run at unsafe rates during SLED treatments.
Baxter Healthcare is recalling 3,440 Prismaflex Control Units worldwide due to reports of operators failing to follow safe unloading instructions and software errors in specific versions.
C.R. Bard is recalling specific lots of HydroSil Gripper Intermittent Catheters because some units were found caught in the sterile barrier seal or cut.
C.R. Bard is recalling Magic 3 Intermittent Catheters because some units were caught in the sterile barrier seal or cut.
GE Healthcare is recalling 355 Monica IF24 Interface Systems because incorrectly reconnected cables can cause fetal and maternal heart rate signals to be displayed incorrectly.
C.R. Bard is recalling Personal Intermittent Catheters because some units were found caught in the sterile barrier seal or cut.
Arrow International is recalling 930 Radial Artery Catheterization Kits because the included povidone iodine prep pads are labeled with an incorrect 36-month shelf life instead of 24 months.
GE Healthcare is recalling 569 units of Centricity PACS-IW because a database error may cause image series to be missing from exams without user notification.
Halyard Health is recalling CORTRAK 2 feeding tubes because the internal stylet may be visible in the exit port window, deviating from specifications.