State
73,817 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,635 recalls naming Georgia we have scored against our rubric, 1,471 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,567 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Garden of Light Inc. is recalling Seven Sundays Vanilla Cherry Pecan Muesli because the product contains almonds but is labeled as containing only pecans.
Keystone RV Company is recalling 2016-2018 Springdale and Summerland recreational trailers because incorrectly connected wiring for electric stabilizer jacks can cause an electrical short and increase the risk of fire.
NeuroLogica Corporation is recalling 87 Samsung GU60A digital X-ray systems because unintended areas are exposed to radiation during the Stitching function.
Neusoft Medical Systems is recalling 154 NeuViz 128 CT scanners due to a software defect. The FDA mandated this Class II recall for units distributed nationwide.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that could cause equipment failure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that can cause equipment failure.
Vyaire Medical is recalling specific lots of AirLife Reduced Heparin Arterial Blood Samplers because they contain incorrect sub-assemblies with larger needles, syringes, and heparin doses.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems due to a cooling system leak that could cause equipment failure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that can cause equipment failure.
Forest River is recalling 2017-2018 Prime Time Wildcat fifth-wheel trailers because the water heater may be installed too close to the slideroom, potentially allowing carbon monoxide to enter the vehicle.
Alcon is recalling 1,074 LuxOR microscope floor stands because casters may break or detach from the base after impact or stress.
Siemens Medical Solutions is recalling 986 AXIOM Artis zee and Q angiography systems in the US due to a cooling system leak that could cause equipment failure.
Smith & Nephew is recalling 402 Polarstem Cardan joints because the device may fracture or fail after multiple uses.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen x-ray systems in the US because a cooling system leak could cause equipment failure.
Optovue is recalling 326 iVue 500 devices because FDA determined a 510(k) is needed for the Vault Mapping software.
Tris Pharma is recalling 34,824 bottles of Morphine Sulfate Oral Solution because the liquid is leaking from the containers.
Neusoft Medical Systems is recalling 234 NeuViz 64 CT scanners due to a software defect. The FDA mandated this recall for units distributed nationwide.
Edwards Lifesciences is recalling specific Fogarty Adherent Clot Catheters because the balloon diameter measures 6mm instead of the intended 10mm.
Optovue is recalling 326 iVue devices because FDA determined a 510(k) is needed for the Vault Mapping software.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US because a cooling system leak could cause equipment failure.
Optovue is recalling 326 iFusion and iVue devices because FDA determined a 510(k) is needed for the Vault Mapping software.
Certified Safety Mfg Inc is recalling sterile burn sheets included in first aid kits because they may shred, potentially failing to protect patients from infection.
KIND, LLC is recalling 4-count boxes of KIND Breakfast Dark Chocolate Cocoa Bars because the outer boxes may be mislabeled and contain KIND Breakfast PROTEIN Dark Chocolate Cocoa Bars.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that can cause equipment failure.
Beckman Coulter is recalling 310 UniCel DxH Slidemaker Stainer units because a fitting may not completely seal after installation.