State
73,827 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.
Which agencies issued them
These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Oxysure Systems is recalling 1,005 Model 615 oxygen cartridges because they do not meet FDA flow rate standards.
Ameritrans is recalling 2015 225 vehicles because the back-up camera may display reversed images, increasing the risk of a crash.
Boehringer Ingelheim is recalling 358,647 Combivent Respimat inhalers because the delivery system may fail to spray properly.
Dairy Farmers of America is recalling Borden Fat Free Sharp Cheddar cheese because a piece of plastic film strip might remain attached to the cheese slice.
Dairy Farmers of America is recalling Borden 2% Pepper Jack White cheese because plastic film strips may remain attached to the slices.
Siemens is recalling ACUSON S2000 and S3000 ultrasound systems with Virtual Touch IQ due to a potential measurement alignment error.
Dairy Farmers of America is recalling Meijer Monterey Pepper Jack cheese slices because a piece of plastic film might remain attached to the cheese.
Dairy Farmers of America is recalling specific Borden Sucrem and Country Fare imitation cheese slices because plastic film may remain attached to the product.
Dairy Farmers of America is recalling various brands of fat free American cheese because a piece of plastic film strip might remain attached to the cheese slice.
Dairy Farmers of America is recalling Borden Sensations Applewood Bacon Cheddar because a piece of plastic film might remain attached to the cheese slice.
Hardy Diagnostics is recalling MDR Acinetobacter and other diagnostic media because they lack FDA 510(k) clearance.
Dairy Farmers of America is recalling fat free pepper jack cheese products because a piece of plastic film strip might remain attached to the cheese slice.
Dairy Farmers of America is recalling Sensations Southwest Pepper Jack cheese because plastic film strips may remain attached to the slices.
Dairy Farmers of America is recalling specific imitation cheese products because a piece of plastic film might remain attached to the cheese slice.
Dairy Farmers of America is recalling Swiss Style Cheese Alternative slices because a piece of plastic film might remain attached to the cheese.
Dairy Farmers of America is recalling specific Swiss imitation cheese products because a piece of plastic film might remain attached to the slices.
Dairy Farmers of America is recalling Hyvee Pepper Jack cheese because plastic film may remain attached to the slices.
Hardy Diagnostics is recalling several microbiology media products, including BEA Broth with Vancomycin, because they lack FDA 510(k) clearance.
Dairy Farmers of America is recalling Borden 2% Light Mozzarella Reduced Fat Slices because a piece of plastic film strip might remain attached to the cheese.
Dairy Farmers of America is recalling SOYA KAAS White Cheddar Flavor Cheese Alternative slices because a piece of plastic film might remain attached to the cheese.
Hardy Diagnostics is recalling specific lots of MacConkey Agar and other diagnostic media because they lack FDA 510(k) clearance.
Dairy Farmers of America is recalling reduced-fat cheese products because a piece of plastic film strip might remain attached to the cheese slice.
Dairy Farmers of America Inc. is recalling imitation pasteurized process cheese food products because a piece of plastic film strip might remain attached to the cheese slice.
Hardy Diagnostics is recalling several microbiology media products, including BEA Agar with VGA, because they lack FDA 510(k) clearance.
Synthes (USA) Products LLC is recalling 31 pre-bent maxillary plates due to potential incorrect laser etch denoting orientation.