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.
First Aid Research is recalling Maximum Strength Bacitraycin Plus Ointment with Lidocaine because the packaging fails to meet child-resistant closure requirements, posing a poisoning risk to young children.
Zevex Incorporated is recalling Moog Curlin Infusion Administration Sets because particulate matter was found on the spike. The recall covers 7,979 cases distributed nationwide and internationally.
Stryker Communications is recalling 850 Berchtold Chromophare Dual Monitor Carrier Arms and Flat Panels because the mounts may have missing or incomplete welds.
Daimler Trucks North America is recalling 2007-2018 Thomas Built Buses Minotour school buses because the wheelchair lift may operate while the vehicle is in motion.
ConMed is recalling STAT 2 I.V. Gravity Flow Needle-Free Controller sets because they exhibit inaccurate or inconsistent flow rates.
M&P Food Productions is recalling Vareniki - farmer cheese due to undeclared wheat. Consumers with celiac disease or wheat allergies should not consume the product.
M&P Food Productions is recalling Vareniki Sour Cherry because the product contains undeclared wheat and Red #40.
BMW is recalling 2018 X3 xDrive30i and M40i vehicles because the rear spoiler may not be properly attached or may be missing screws, posing a road hazard.
Hitachi Medical Systems America Inc is recalling 55 ultrasound transducers (Model UST-5550-R) because they may not have adequate protection against electrical shock hazards.
M&P Food Productions is recalling Vareniki Cabbage because the product contains undeclared wheat. Consumers with celiac disease or wheat allergies should not eat the product.
M&P Food Productions is recalling Hand Made Russian Style Blintzes because they contain undeclared wheat. Consumers should check their pantries for the affected product.
LifeCell is recalling 25,798 units of the Revolve Advanced Adipose System due to bacterial endotoxin levels above acceptable limits.
Zevex Incorporated is recalling specific lots of Moog Curlin Infusion Administration Sets due to particulate matter found on the spike.
Siemens Medical Solutions is recalling Axiom Artis devices due to a potential for liquid entry.
Fresenius Medical Care is recalling 15 hemodialysis machines due to a software error that causes a discrepancy between the displayed and actual ultrafiltration rates.
Tosoh Bioscience is recalling ST AIA-PACK Prog II assay kits because DHEA-S supplements can cause falsely elevated progesterone results.
Zevex Incorporated is recalling specific lots of Moog Curlin Infusion Administration Sets because particulate matter was found on the spike.
M&P Food Productions is recalling Hand Made Russian Style Blintzes because they contain undeclared wheat and FD&C Red #40.
Zimmer Biomet is recalling 38,069 units of Versys 6 inch Beaded Full Coat Plus Hip Prostheses because weight issues may have compromised the sterile barrier.
Philips is recalling 1,486 Allura Xper FD and ORT X-ray systems because extra monitors mounted on the ceiling suspension may disengage and fall.
Accord Media, LLC is recalling 30 units of the Truth Renew device because it uses an unapproved green LED light to treat hyperpigmentation.
Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.
Trumpf Medical Systems is recalling 212 surgical camera systems because their wireless receivers emit radiation above accepted limits, potentially interfering with other operating room devices.
Accord Media is recalling 67 units of the Truth Renew Plus device because it uses an unapproved green LED light to treat hyperpigmentation.
Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.