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.
East Manufacturing is recalling 2016-2018 Frame Dump trailers because cracks in the cross member may cause failure, increasing crash risk.
Honda is recalling specific 2010, 2016, and 2017 VT1300CX Fury motorcycles because missing welds on the fuel tank mounting bracket could cause fuel leaks and fire.
Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Almonds because the product contains undeclared milk (casein).
Won Industry Co. is recalling three unapproved Compressible Limb Therapy Systems because they have incorrect air compression level setups. The devices were distributed in Maryland, Texas, and Mexico.
H. A. R. Maspeth Corp. is recalling Woldong World's Best Kimchi due to undeclared sesame seeds. The product was distributed in nine states.
Leclerc Foods USA is recalling Fit & Active Chocolatey Chip Protein Meal Bars because flexible pieces of yellow plastic were found in the product.
Biosense Webster is recalling 185 SMARTABLATE RF System Generators because they may inadvertently deliver RF energy if the foot pedal is placed near Stereotaxis magnets.
Becton Dickinson is recalling 2,598,000 BD Precision Glide Needles due to hub damage that can cause breakage or leakage during use.
Pro-Med Instruments is recalling DORO Sterile Disposable Skull Pins because two instances of pin tip breakage were reported during surgery.
Roche Diabetes Care is recalling the Accu-Chek Connect app because a bug in the Bolus Advisor feature may prevent correction bolus advice from being available for recent glucose readings.
ICU Medical Inc is recalling MedNet 6.1 and 6.21 software because it may alter piggyback medication settings without user notice.
Biosense Webster is recalling PENTARAY NAV High-Density Mapping Catheters because the instructions for use were updated to indicate they should not be used in patients with prosthetic valves.
Krispy Kreme is recalling Original Glazed Doughnuts because a foreign matter strand was found on the product. The recall affects 4,041 boxes and containers distributed in Georgia and South Carolina.
Krispy Kreme is recalling Original Glazed Doughnut Holes because a foreign matter strand was found in the product. The recall affects boxes sold in Georgia and South Carolina.
The Kroger Co. is recalling Comforts FOR BABY Purified Water with Fluoride Added after a complaint of mold was found in the product.
DeRoyal is recalling sterile custom surgical kits containing Medline Aplicare Povidone Iodine Prep Pads due to incorrect expiration dates.
Novo Nordisk is recalling specific batches of Dial-A-Dose insulin pen cartridge holders because they may crack or break when exposed to certain cleaning agents.
Krispy Kreme is recalling specific lots of doughnuts and doughnut holes found with a foreign strand. Consumers in Georgia and South Carolina should discard these products.
Krispy Kreme is recalling Glazed Mini Crullers because a foreign matter was found on the product. The recall affects 4,041 boxes and containers distributed in Georgia and South Carolina.
Krispy Kreme is recalling Glazed Pumpkin Spice Cake Doughnuts because a foreign matter strand was found in the product. The recall affects 4,041 boxes sold in Georgia and South Carolina.
Krispy Kreme is recalling Glazed Blueberry Cake Doughnuts because a foreign matter strand was found in the product. The recall affects 4,041 boxes distributed in Georgia and South Carolina.
Krispy Kreme is recalling Glazed Mini Crullers because a foreign strand was found in the product. The recall affects 4,041 boxes sold in Georgia and South Carolina.
Won Industry Co. is recalling two Morning Life air compression devices because they were distributed without FDA approval and have incorrect air compression settings.
Fukuda Denshi is recalling DS-8100M and DS-8100N patient monitors because a damaged lithium-ion capacitor may cause a short-term battery error message.
Biosense Webster is recalling 73,796 PENTARAY NAV High-Density Mapping Catheters to update contraindication language in the Instructions For Use regarding prosthetic valves.