State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Merge Healthcare is recalling iConnect Access software versions 3.0.1, 3.1, and 3.2 because the software displayed incorrect prior reports when viewing multiple studies.
Siemens is recalling ADVIA Centaur CA 19-9 Assay kits because they do not meet performance standards on the ADVIA Centaur CP system.
Beckman Coulter is recalling Access Ostase Calibrators because they do not meet expiration date claims within 10% criteria.
Siemens is recalling ADVIA Centaur CA 19-9 Assay kits because they do not meet performance standards on the ADVIA Centaur CP system.
Siemens Healthcare Diagnostics is voluntarily recalling 448 FlexLab Automation Modules. The recall was initiated by the firm and is classified as Class II.
Sorin Group USA is recalling 586 Orchestra Plus programmers because their residual longevity estimates may be inaccurate, potentially affecting patient monitoring.
C.R. Bard is recalling 10,290 units of Magic3 catheters labeled as hydrophilic but lacking the coating.
C.R. Bard is recalling 75,089 Bard Inlay Ureteral Stents to add a warning about potential knots during removal.
Siemens Healthcare Diagnostics is recalling Dimension IRON Flex reagent cartridges because deferoxamine interferes with the assay at a different concentration than listed in the instructions.
Philips Medical Systems is recalling three IQon Spectral CT systems because the product labels do not include the correct current rating.
Philips Medical Systems is recalling 67 Brilliance iCT Computed Tomography X-ray systems because the product labels do not include the correct current rating.
Philips is recalling 15 Ingenuity Core 128 CT scanners because the product labels do not include the correct current rating.
CutisPharma is recalling 5,904 kits of FIRST Omeprazole 2mg/mL because the package insert incorrectly lists the strength as 3mg/mL.
GSK Consumer Healthcare is recalling Zeasorb AF antifungal cream because some bottles have incorrect NDC codes or indications on the labels.
Siemens Healthcare Diagnostics is recalling Dimension Vista IRON Flex reagent cartridges due to deferoxamine interference at concentrations not listed in the Instructions for Use.
CutisPharma is recalling 8,748 Omeprazole compounding kits because the package insert incorrectly lists the strength as 3mg/mL instead of 2mg/mL.
Stryker is voluntarily recalling Care Instructions for the RF MultiGen Generator because they incorrectly support sterilizing the cables.
Philips is recalling two Ingenuity Core CT systems because the product labels do not include the correct current rating.
Philips is recalling three Brilliance ICT SP CT systems because the product labels do not include the correct current rating.
Philips is recalling 27 Ingenuity CT systems because the product labels do not include the correct current rating.
H.J. Heinz is recalling approximately 5,022 pounds of bistro au jus gravy that was incorrectly labeled as pork gravy. The product contains undeclared milk and soy allergens.
BRP is recalling about 2,380 model year 2017 Can-Am Maverick X3 side-by-side off-road vehicles because a steering defect can cause loss of control and crashes.
Forest River is recalling certain 2017 XLR Toyhauler trailers because they may have an incorrect Federal Placard that fails to indicate a third axle.
Nissan is recalling 12,112 model year 2016 Titan XD diesel vehicles because a fuel tank breather tube may not be properly connected, causing inaccurate fuel gauge readings.
E-One is recalling 2010-2016 Cyclone vehicles because suspension air bags may lose pressure and fail, increasing crash risk.