State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Biomet 3i, LLC is recalling Preformance Post Dental implants because pouches may not have been sealed during packing.
Medtronic is recalling Valleylab Laparoscopic Flexible Argon Blade Electrodes because the packaging may be compromised, potentially breaching the sterile barrier.
Biomet 3i, LLC is recalling specific Gingihue Post dental implants because pouches may not have been sealed during packing.
Medtronic is recalling 6,720 Valleylab Laparoscopic Straight Spatula Electrodes because the package may be compromised, potentially breaching the sterile barrier.
Biomet 3i is recalling Locator Light Retention Replacement Males because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Prep-tite Cap Dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling Pick-Up Impression Coping dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling certain Pick-Up Coping dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Preformance Temporary Cylinder Dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Standard Abutment Transfer Coping Dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling 1,648,273 dental implant devices because pouches may not have been sealed during packing.
Biomet 3i is recalling Locator Abutment dental implants because pouches may not have been sealed during packing.
Teleflex Medical is recalling 45 units of the Weck EFx Classic Fascial Closure System because incorrect expiration dates were printed on the labels.
Biomet 3i is recalling Conical EP Pick-Up Coping dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling EP Twist Lock Coping Dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling certain Bellatek Encode Healing Abutment dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling certain Gingihue Post Dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Locator Abutment dental implants because pouches may not have been sealed during packing.
Jumping Jack is recalling 2014-2015 utility trailers because a small torsion arm may detach, causing loss of stability and increasing crash risk.
Land Rover is recalling certain 2014-2015 Range Rover Evoque and 2015 Discovery Sport vehicles because the transmission may unexpectedly shift to neutral, increasing crash risk.
Arctic Cat is recalling about 4,500 side-by-side utility vehicles because a stuck throttle cable can prevent the vehicle from returning to idle, posing a crash hazard.
Morbark is recalling 2013-2016 Beever M15R and M20R wood-chipper trailers because stop and tail lights may be positioned too high to be easily seen, increasing crash risk.
ALEX Toys is recalling three infant building sets because small parts can detach, posing a choking hazard to young children.
McDonald's is recalling Step-iT activity wristbands because they can cause skin irritation or burns. Consumers should remove the bands from children and return them for a free replacement.
Crownplace Brands is recalling Aladdin MaxBrite kerosene lamp burners because the threads can disengage, posing burn and fire hazards.