State
72,940 recalls have nationwide distribution and so reach Nebraska. 4,547 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,547 recalls naming Nebraska we have scored against our rubric, 705 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,119 (25%) are Severe.
Which agencies issued them
These figures cover only the 4,547 recalls whose distribution notice names Nebraska specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Get Tested International AB is recalling 16 units of its Allergy & Food Intolerance Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1 unit of its Food Sensitivity Test Medium because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its GI Microbiome Profile XL because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 48 units of its Diabetes Test (ketones & glucose) because the product was distributed without premarket approval or clearance.
Siemens Medical Solutions USA is recalling 6 MAMMOMAT Inspiration systems because operator tables were sold together with a bus-installation kit they are not released for.
Get Tested International AB is recalling 24 units of its Akkermansia Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1 unit of its Alcohol (ALC) Test Saliva because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 2043 units of its 8 in 1 STI Test Kit because the product was distributed without premarket approval or clearance.
Fresenius Kabi USA is recalling 15,862 Ivenix Infusion System large volume pumps because downstream occlusion alarms may occur at low flow rates when a check valve is added to the administration set.
Get Tested International AB is recalling 16 units of its Food Intolerance Test Medium because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 18 units of its Neurotransmitters Basic because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 94 units of its Parasite Test because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 14700 bottles of Globe Clotrimazole Cream USP over current good manufacturing practice deviations.
Get Tested International AB is recalling 5 units of its Food Intolerance Test Small because the product was distributed without premarket approval or clearance.
Siemens Medical Solutions USA is recalling one MAMMOMAT Fusion system because an operator table was sold together with a bus-installation kit it is not released for.
Get Tested International AB is recalling 71 units of its Allergy Test IgE because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 7,920 bottles of Nivagen Zinc Oxide Ointment USP 20%, 1 oz, over current good manufacturing practice deviations.
Get Tested International AB is recalling 6 units of its Gut Microbiome Test Small because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 109 units of its Candida Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 27 units of its PSA Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 55 units of its SIBO Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its Gut Microbiome Test Large because the product was distributed without premarket approval or clearance.
Philips North America is recalling 6 CT 5300 systems because a tube heat exchanger whose screws are not tightened after replacement may detach and damage other components.
Get Tested International AB is recalling 14 units of its Neurotransmitters XL because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1 unit of its Drug Test Small (4 substances) because the product was distributed without premarket approval or clearance.