State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Abbott Point Of Care Inc. is recalling 894 i-STAT DE handheld data processing modules because a software upgrade resets customized settings and prevents certain data from updating.
Bausch & Lomb is voluntarily recalling 1,236,749 LaserEdge Knives intended for ophthalmic surgery due to an atypical volume of complaints regarding dull blades.
Bausch + Lomb is voluntarily recalling 1,236,749 LaserEdge Knives intended for ophthalmic surgery due to an atypical volume of complaints regarding dull blades.
Hospira Inc. is recalling Labetalol Hydrochloride Injection vials because of cracked glass at the rim, which is covered by the stopper and crimp seal.
Bausch + Lomb is voluntarily recalling specific LaserEdge ophthalmic knives because an atypical volume of complaints reported dull blades.
Bausch & Lomb is voluntarily recalling specific LaserEdge ophthalmic knives because of an atypical volume of complaints regarding dull blades.
Ortho-Clinical Diagnostics is recalling VITROS DAT Performance Verifier V units due to storage labeling errors that may cause lower than expected VITROS BENZ results.
Bausch & Lomb is voluntarily recalling 1,236,749 LaserEdge Knives used in ophthalmic surgery because of an atypical volume of complaints regarding dull blades.
Instrumentation Laboratory is recalling 14,894 Hemosll ReadiPlasTin kits due to reported performance issues, including increased imprecision and out-of-range quality controls.
Springside Cheese Corp is recalling Monterey Jack Tomato Basil Cheese because it may have been made with milk held for 13.8 seconds during pasteurization.
SCA Pharmaceuticals is recalling 480 syringes of labetalol HCl injection because some labels display incorrect compounding and use-by dates.
Akorn, Inc. is recalling 31,812 bottles of Atropine Sulfate Ophthalmic 1% Solution because testing revealed low viscosity results.
AstraZeneca is recalling 18,056 bottles of Lynparza (olaparib) capsules 50 mg due to elevated levels of a specific quality attribute.
Amazon is recalling about 260,000 portable power banks because the batteries can overheat and ignite, posing fire and chemical burn risks.
MAAX Spas is recalling about 550 hot tubs and swim spas in the U.S. because the internal UV generator can ignite, posing a fire hazard.
Honda is recalling 2014-2016 Odyssey vehicles because the second row left outboard seatback may fail to lock, increasing injury risk in a crash.
Helvetia Sports is recalling SwissStop EXOTherm cycling disc brake pads because they can separate from the backplate, posing a fall hazard to users.
Autocar is recalling 1,320 Xpeditor vehicles equipped with factory-installed methane detection systems because inadequate circuit protection may cause the wiring harness to overheat, increasing the risk of a fire.
Ford is recalling 2013-2016 Focus and Fusion vehicles with manual transmissions because the clutch may fracture, causing transmission damage and fluid leaks that could lead to fire.
Daimler Trucks North America is recalling 9,480 Freightliner Custom Chassis vehicles due to a power steering hose defect that may cause electrical arcing and fire.
Ford is recalling 2014-2018 Fusion and Lincoln MKZ vehicles because the steering wheel bolt may loosen, allowing the wheel to detach and causing loss of control.
Hyundai is recalling 2016-2018 Sonata Plug-In Hybrids because a voltage protection device may activate inadvertently, causing loss of power and increasing crash risk.
SynTec Seating Solutions is recalling S3B Non-Restraint Wall Mounted Seats because the mounting bracket may crack, increasing injury risk in a crash.
Forest River is recalling 2018 Stealth Evo recreational trailers because the federal placard lists incorrect tire sizes. This error could lead owners to install wrong replacement tires, increasing crash risk.
Ferrari is recalling 2016 488 GTB and 488 Spider vehicles because a software error may prevent drivers from receiving warnings about critically worn brake discs.