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.
About 2,650 Uuoeebb infant walkers are being recalled because they can fit through a standard doorway and fail to stop at the edge of a step, and their leg openings can entrap a child's head.
Fresenius Kabi USA is recalling 483 cases of Ivenix LVP Primary Administration Sets after incorrect assembly of a specific lot that the firm states could result in serious patient injury.
Bridgestone is recalling Firestone Destination LE3 tires because a belt edge insert may be out of position, causing tread separation and increasing crash risk.
Lucid is recalling 2026 Gravity vehicles because incorrect seat covers may prevent side air bags from deploying correctly, increasing injury risk.
Philips North America is recalling the IntelliVue Patient Monitor MX550 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP80 over a potential issue where the monitors did not alarm.
Great Lakes Cheese is recalling 15,490 cases of Italian style shredded cheese blend, sold under eight brands, over potential metal fragments originating in a supplier raw material.
Costco is recalling 142,532 retail units of Kirkland Signature Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Philips North America is recalling the IntelliVue Patient Monitor MX800 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP2 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP50 over a potential issue where the monitors did not alarm.
Illumina is recalling 11,916 NextSeq 550Dx reagent kits because flow cell gaskets have a quality issue that may cause leaks during runs, including possible toxic substance exposure to the user.
Great Lakes Cheese is recalling 4,298 cases of pizza style shredded cheese blend, sold under six brands, over potential metal fragments originating in a supplier raw material.
Enterix is recalling 201,426 InSure ONE Fecal Immunochemical Test kits after the test failed sensitivity testing with one test card lot, which may result in false negative results.
Philips North America is recalling the IntelliVue Multi Measurement Server X2 over a potential issue where the monitors did not alarm.
Medtronic is recalling 6,591 Aurora EV-ICD and Clinical EV-ICD single chamber extravascular defibrillators over the potential for delayed time to high-voltage therapy in a rare sequence of events.
Philips North America is recalling the IntelliVue MP90 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP20 over a potential issue where the monitors did not alarm.
Blue Bird is recalling 2025-2027 Vision school buses because a missing support brace may cause the wheelchair lift to fail, increasing injury risk.
Water Pure is recalling 17,612 bottles of My Bladder dietary supplement because the product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303.
Blue Bird is recalling 2026-2027 Vision and All American school buses because wheelchair restraints may fail to lock, increasing injury risk.
Philips North America is recalling the IntelliVue Multi-Measurement Module X3 over a potential issue where the monitors did not alarm.
Great Lakes Cheese is recalling 1,850 cases of Good & Gather Mozzarella & Parmesan shredded cheese blend over potential metal fragments originating in a supplier raw material.
Philips North America is recalling the IntelliVue Patient Monitor MX850 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP5 over a potential issue where the monitors did not alarm.