State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Siemens is recalling 492 RAPIDPoint 400 Blood Gas Analyzers because patient names may be printed with data from a different patient.
ICU Medical is recalling specific Transpac IV Monitoring Kits because of a potential leak in the SafeSet Reservoir and blood sampling components.
ICU Medical is recalling specific Transpac IV Monitoring Kits because of a potential leak in the SafeSet Reservoir and blood sampling components.
Haitai is recalling Matdongsan Peanut Crunch Snack because it contains undeclared soy lecithin. The recall affects specific lot codes distributed across 18 states.
ICU Medical is recalling 10 units of SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.
ICU Medical is recalling 110 units of Double Kit with SafeSet and 03mL Flush Device due to a potential for leak.
Mars Chocolate North America is recalling Combos Pepperoni Pizza Crackers due to the potential for undeclared peanut residue. The recall affects 183,678 cases distributed nationwide and in foreign markets.
Hostess Brands is recalling Donettes Maple Glazed Mini Donuts because the product contains peanut allergen but is not labeled to contain peanuts.
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.
Reese Pharmaceutical is recalling Good Neighbor Pharmacy Cranberry Tablets because the label omits calcium and lists the wrong serving size.
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.