State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Smith & Nephew is recalling nine Biosure Ratchet Drivers because they are oversized and may not fit screws properly or may cause screws to stick.
Pfizer is recalling specific lots of Lyrica (pregabalin) 50 mg capsules due to the potential presence of deformed or damaged capsules.
Smith & Nephew is recalling 157 Biosure Drivers that are oversized and may fail to insert screws properly or cause screws to stick.
Olympus is voluntarily removing all TJF-Q180V duodenoscopes to replace the forceps elevator mechanism with a new design consistent with recent 510(k) specifications.
Siemens Healthcare Diagnostics is recalling 87 ADVIA Chemistry XPT Systems due to software defects that may cause test failures, calibration errors, and system restarts.
Horiba Instruments Inc is recalling 216 units of ABX PENTRA Cholesterol CP reagent because N-acetylcysteine can cause falsely low results.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur PSA Assay kits because they do not meet the High Dose Hook Effect expectation in the Instructions for Use.
Perrigo Company PLC is recalling Nystatin, USP Powder for Rx compounding due to a labeling error regarding the declared strength.
Horiba Instruments Inc is recalling ABX PENTRA Triglycerides CP assays because N-acetylcysteine in patient blood can cause falsely low results.
Horiba Instruments Inc is recalling ABX PENTRA Glucose reagents because N-acetylcysteine in patient blood can cause falsely low glucose results.
Baxter is recalling RAPIDFILL Syringe Strips because the packaging claims a 12-month shelf life without supporting evidence.
Mylan Institutional, Inc. is recalling Clonazepam Tablets, 0.5 mg, because a known impurity exceeded specifications at the 6-month timepoint.
Honda is recalling 2016 Civic vehicles with 2.0L engines because missing or incorrect piston circlips may cause engine seizure, increasing the risk of a crash or fire.
Kalmar is recalling 622 Ottawa T2 trucks from 2014-2016 because an unprotected power board may cause an electrical short and fire.
Classic Characters is recalling infant knit Elf Booties because the toe pompoms can detach, posing a choking hazard to young children.
Haier is recalling 55-inch LED televisions installed in fifth-wheel recreational vehicles because mounting brackets may separate, causing the TVs to fall.
IKEA is recalling HYBY and LOCK ceiling lamps because plastic clips can break, causing glass shades to fall and pose a laceration hazard.
Vosges, LTD is recalling 135 pounds of Uncured Bacon Ganache chocolate bars sold at Trader Joe's in four states because the product contains undeclared coconut, a known allergen.
Stoughton is recalling 2015-2016 Barrett P gooseneck trailers because the upper coupler rating is lower than the trailer's GVWR, risking separation.
PACCAR is recalling 2015-2016 Peterbilt 365 and 367 trucks because improperly tightened drive axle nuts may cause the driveshaft to disconnect, increasing crash risk.
BMW is recalling approximately 840,000 vehicles because the driver's frontal air bag inflator may rupture during deployment, potentially causing serious injury or death.
General Motors is recalling specific 2015-2016 Chevrolet and GMC trucks and SUVs because the brake pedal pivot nut may loosen, potentially making the brake pedal inoperative.
Toyota is recalling specific 2003-2006 Land Cruiser, LX470, Tundra, Sequoia, 4Runner, and GX470 vehicles because side air bags may deploy unexpectedly, increasing injury risk.
Kia is recalling 2011 Fortes because a defective transmission cooler hose may leak fluid, potentially causing the vehicle to stop moving and increasing crash risk.
Genie is recalling 2016 TZ-34/20 trailer-mounted boom lifts because bolts attaching the turntable may not be properly tightened, posing a risk of platform fall and injury.