State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Immuno-Mycologics is recalling 630 units of the Cryptococcal Antigen Lateral Flow Assay because specific lots have lower specificity, leading to reported false positive results.
Zimmer Biomet is recalling Vanguard Total Knee System femoral components because packaging labels may incorrectly identify the size or side of the implant.
Ortho-Clinical Diagnostics is recalling VITROS Na+ Slides because they may produce biased results if stored on the analyzer for 10 days after minimum warm-up.
Siemens Medical Solutions USA is recalling 55 Mammomat Inspiration digital x-ray mammography systems due to a software error.
Roland Foods is recalling Manzanilla Olives Stuffed With Anchovies because FDA sampling found non-pathogenic Gram Positive Rods.
Sony is expanding a recall of Panasonic lithium-ion battery packs used in VAIO laptops due to overheating risks that can cause burns and fires.
Cruiser RV is recalling 2016-2017 Boss recreational trailers because a vertically-mounted furnace may have exhaust ports at the top, creating an unsafe operating condition.
Lamborghini is recalling 2012-2017 Aventador vehicles because gasoline may contact the exhaust system, increasing the risk of a fire.
Volkswagen is recalling 2017 Jetta vehicles with 1.4L engines because the engine block may be improperly cast, potentially causing the engine to seize and leading to a loss of vehicle control.
REV Recreation Group is recalling 391 Holiday Rambler and Fleetwood motorhomes because a spring shackle bolt may puncture fuel components, creating a fire hazard.
Midwest Fire Equipment is recalling one 2017 All-Poly 3000 Series vehicle because the stop light switch may fail to illuminate brake lights, increasing crash risk.
Nissan is recalling 2002 Pathfinder and Infiniti QX4 vehicles because the front passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Walt Disney Parks and Resorts is recalling Happy Holidays! Mickey Mouse Nightlights because liquid can leak onto electrical outlets, posing a fire hazard.
BMW is recalling specific 2011-2012 models because the rear driveshaft CV joint may break, causing loss of propulsion and increasing crash risk.
Jayco is recalling 2017 Seismic and Seismic Wave fifth-wheel trailers because improper wiring may prevent the breakaway switch from functioning, increasing crash risk.
Restoration Hardware is recalling approximately 1,400 Venetian style glass mirrors because they may detach from the backing, posing a laceration hazard.
Boulder Brands is recalling Earth Balance Vegan Mac and Cheese products due to undeclared milk, a major allergen.
Highland Ridge RV is recalling 2016-2017 Open Range fifth-wheel vehicles because axle hangers may puncture the riser tube, causing axle misalignment and tire failure.
Roche Diabetes Care is recalling the Accu-Chek Connect app because software defects may cause incorrect insulin bolus recommendations, potentially leading to hypoglycemia.
Boulder Brands is recalling Earth Balance Vegan Mac and Cheese products because they contain undeclared milk, a major allergen.
Soft Computer Consultants is recalling Softbank II software due to a software error that may produce incorrect results in transfusion services.
Roche Diagnostics is recalling 30 cobas b 123 POC systems because a software issue may prevent automatic quality control from running, potentially leading to undetected incorrect test results.
Baxter Healthcare is recalling Phoenix Dialysis Machine Preventive Maintenance Kits due to incorrect silicone connectors that may cause fluid leaks.
Medline Industries is recalling Unna-Z compression wraps due to contamination with common mold species. The recall affects units distributed in the US and several international countries.
Atrium Medical is recalling Pediatric Chamber Ocean Drains because the outer packaging is not sterile. The recall covers units with expiration dates prior to October 2019.