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.
Siemens is recalling 144 RAPIDLab 1240 Blood Gas Analyzers because patient names may be printed with data from a different patient.
Mars Chocolate North America is recalling Combos Buffalo Blue Cheese Pretzels due to potential undeclared peanut residue.
ICU Medical is recalling 760 Transpac IV Trifurcated Monitoring Kits because of a potential for leaks in the SafeSet Reservoir and blood sampling components.
ICU Medical is recalling 125 SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.
Mars Chocolate North America is recalling Combos Cheddar Cheese Crackers due to potential undeclared peanut residue.
ICU Medical is recalling 10 units of SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.
Howmedica Osteonics Corp. is recalling AccuLIF PL Cages because some implants have shown a reduction in height greater than 1 mm after surgery.
ICU Medical is recalling specific SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.
Mars Chocolate North America is recalling Combos Pizzeria Pretzels due to potential undeclared peanut residue. The recall covers 183,678 cases distributed nationwide and abroad.
Hostess Brands is recalling Zingers Raspberry cakes because they were made with flour containing peanut allergen but are not labeled to contain peanuts.
Clark Laboratories is recalling specific lots of the Captia Measles IgM test kit because the product failed quality control stability testing.
Mentor Texas, LP. is recalling 48 Artoura Breast Tissue Expanders because CPX4 devices may have been packaged in Artoura boxes.
Mentor Texas, LP. is recalling 30 units of CPX4 Breast Tissue Expanders because they may have been packaged in the wrong box.
Kill Cliff is recalling Strawberries & Cream Protein Bars because they may contain mold. The recall started on June 21, 2016.
Integra LifeSciences is recalling 14 packages of Meshed Dermal Regeneration Template due to an incorrect calculation of peel strength test results.
Amerisource Health Services is recalling 2,626 bottles of bupropion hydrochloride extended-release tablets due to failed dissolution specifications.
Siemens is recalling 101 Syngo Plaza PACS systems because a suffix on DICOM images may indicate that displayed measurements differ from actual values.
Sysmex America Inc is recalling Fluorocell PLT reagent because it may produce falsely low platelet results on Sysmex XN-Series analyzers.
Siemens is recalling 101 Syngo.Plaza VB 10 A image processing systems because a suffix on DICOM images may indicate that displayed measurement values differ from real values.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 31, Lot 3155, because an incorrect value on the Assay Data Disks prevents successful calibration of the HbA1c assay.
Biomerieux is recalling 229 VIDAS NT-pro-BNP kits because they contain the incorrect number of control vials.
Alere San Diego, Inc. is recalling LDX Optical Check Cassettes because the expiration date on the magnetic strip does not match the labeled date.
New Flyer is recalling 38 model year 2016 XN60 and XN40 transit buses because a pressure relief device may fracture, releasing high-pressure gas and increasing fire risk.
Ducati is recalling 2016-2017 XDiavel motorcycles because a loose final drive pulley nut may cause loss of power to the rear wheel, increasing crash risk.
Porsche is recalling specific 1L and 30L brake fluid containers manufactured between September 2015 and August 2016 because they lack the required 'DOT 4' label, posing a risk of incompatible fluid use.