State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Philips North America is recalling the IntelliVue Patient Monitor MX750 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX400 over a potential issue where the monitors did not alarm.
Hale inc is recalling 54 bottles of Lotsa Pasta Roasted Garlic Infused Olive Oil over the potential for Clostridium botulinum contamination.
Great Lakes Cheese is recalling 4,131 cases of mozzarella and provolone shredded cheese blend, sold under four brands, over potential metal fragments from a supplier raw material.
Great Lakes Cheese is recalling 235,789 cases of low-moisture part-skim mozzarella shredded cheese, sold under 26 brands, over potential metal fragments from a supplier raw material.
Philips North America is recalling the IntelliVue MP60 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX500 over a potential issue where the monitors did not alarm.
Costco is recalling 612 retail units of Kirkland Signature Chicken Sandwich with Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Philips North America is recalling the IntelliVue MP30 over a potential issue where the monitors did not alarm.
Blonde Beard's is recalling 4,888 8 oz bottles of Dojo Asian Wing Sauce because the product contains undeclared soy.
Philips North America is recalling the IntelliVue MP70 over a potential issue where the monitors did not alarm.
Prime Food Processing is recalling frozen Lava Bun with Green Tea Flavor because the products do not declare milk in the Contains statement or the ingredient statement.
Great Lakes Cheese is recalling 117 cases of Food Club Finely Shredded Pizza Style Four Cheese Blend over potential metal fragments originating in a supplier raw material.
Prime Food Processing is recalling 2,243 cases of frozen Lava Bun with Salted Egg Yolk because the products do not declare milk in the Contains statement or the ingredient statement.
Great Lakes Cheese is recalling 1,900 cases of Happy Farms by Aldi Italian Style shredded cheese blend over potential metal fragments originating in a supplier raw material.
Philips North America is recalling the IntelliVue Patient Monitor MX100 over a potential issue where the monitors did not alarm.
Breckenridge Pharmaceutical is recalling 3,397 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Breckenridge Pharmaceutical is recalling 7,389 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Volkswagen is recalling 3,138 model year 2025 Tiguan vehicles because a fault in the passenger occupant detection system wiring may deactivate the front passenger air bag when the seat is occupied.
Motor Coach Industries is recalling various transit bus models because the front door lower curb view glazing material is incorrect, which may reduce driver visibility and increase crash risk.
Philips North America is recalling the IntelliVue Patient Monitor MX600 over a potential issue where the monitors did not alarm.
Ventura Foods is recalling 700 cases of Publix Deli Carolina-Style Mustard BBQ Sauce after foreign objects, described as black plastic planting material, were found in granulated onion.
Philips North America is recalling the IntelliVue Patient Monitor MX450 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX700 over a potential issue where the monitors did not alarm.
Accriva Diagnostics is recalling 20,250 Hemochron Activated Clotting Time Low-Range test cuvettes because a foreign object with sharp edges may pose a risk of injury if not detected before handling.