State
73,598 recalls have nationwide distribution and so reach Nebraska. 4,576 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,576 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 4,576 recalls whose distribution notice names Nebraska specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Bridgestone is recalling specific Firestone and Bridgestone tires that may have a pinhole in the sidewall, which can cause slow air leaks and increase crash risk.
Volkswagen Group (Audi) is recalling 2020-2021 S5, A5, and RS5 vehicles due to missing anti-abrasion protection on rear light wiring. In a crash, exposed wires may be damaged, potentially disabling door locks and hazard lights.
Lidl US is recalling Powerfix Steel Shelving Units because missing wall mounting hardware creates tip-over and entrapment risks. Consumers should stop using the units if not wall-mounted.
Merit Medical Systems is recalling Cultura Flex Swabs because the flocked tip may break off during use, potentially causing soft tissue injury or treatment delays.
Thomas Scientific is recalling Wuxi Nest patient specimen collection tubes to replace units manufactured and distributed prior to Enforcement Discretion Approval.
Santa Cruz Bicycles is recalling about 2,900 model year 2020 aluminum frames because thermal damage can cause them to bend or buckle, posing a fall hazard.
RH is recalling approximately 7,800 wine barrel chandeliers because hanging hardware can break, causing the fixture to fall. No injuries have been reported.
Certain 2020-2021 Toyota RAV4, RAV4 Hybrid, Avalon, and Avalon Hybrid vehicles may have damaged steering column breakaway pins that could reduce airbag performance in a crash. Toyota will replace the steering column at no cost.
Kibbi is recalling certain 2019-2021 Renegade motorhomes with Dometic cooking stoves due to a potential gas leak from an overtightened saddle valve bolt, which could increase fire risk. Dealers will install repair kits free of charge.
Stryker is recalling Mako MICS Handpieces due to a characterization issue that may cause unsuccessful checkpoint verification or bone cuts differing from the preoperative plan.
Cardinal Health 200, LLC is recalling Kangaroo Connect 1000ml Bag Sets because the feeding spike sets may leak at the tube and spike connector interface.
Merit Medical recalls its Cultura Collection and Transport System because the swab tip may break off during sample collection, potentially causing soft tissue injury.
Roche Diagnostics is recalling 40 cobas infinity central lab licenses because an erroneous QC status may cause incorrect validation of results.
General Motors is recalling 2015-2016 Chevrolet Silverado and GMC Sierra trucks because the roof-rail air bag inflator end cap may detach, posing an injury risk.
Merit Medical is recalling Cultura Collection and Transport Systems because the swab tip may break off during sample collection, potentially causing soft tissue injury.
Herobility is recalling Eco Baby Spoons, Forks, and Feeding Sets because they can break into small pieces, posing a choking hazard. No injuries have been reported.
Front seat attachment bolts may not have been properly installed on certain 2021 Chevrolet Tahoe, Suburban, and GMC Yukon models. If loose or missing, the seats could move during a crash, increasing injury risk.
Siemens Healthcare Diagnostics is recalling Atellica IM 1300 Analyzers because scanning specific test definitions may reset custom settings, causing inaccurate test results.
Ortho Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 IgG Control and Calibrator lots due to elevated signal/cutoff values and decreased signal.
LivaNova is recalling 134 VNS Therapy AspireSR Generators because an extra digit in the serial number makes them incompatible with specific therapy programmers.
Apotex Corp. is recalling Aripiprazole Tablets 15 mg because they failed to meet dissolution specifications. The affected products were distributed nationwide in the USA.
Siemens is recalling 26 Artis X-ray systems worldwide because incorrect diodes may fail to protect against overvoltage, potentially causing system malfunction.
Hikma Pharmaceuticals is recalling specific lots of Sodium Chloride Injection USP 0.9% 2 mL vials because they failed pH specifications.
Siemens Healthcare Diagnostics is recalling Atellica IM 1600 Analyzers because scanning a new kit lot may reset custom settings to defaults.
Ortho Clinical Diagnostics is recalling specific lots of VITROS SARS-CoV-2 IgG Calibrators because they produced elevated signal values. The recall also includes one lot of IgG Controls with decreased signal.