State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling 2019 Ram 1500 vehicles because an improperly secured battery ground fastener may cause loss of power steering assist, increasing crash risk.
Honda is recalling 2017-2019 Ridgeline trucks because exposure to acids can crack the fuel pump feed port, creating a fire hazard.
Mack Trucks is recalling 2019-2020 Anthem, Granite, and Pinnacle vehicles because the passenger-side door mirror may detach, posing a risk of injury or crash.
Chrysler is recalling 2019 RAM 1500 trucks with 12-inch touchscreens and base HVAC systems because the windshield defroster does not work, increasing crash risk.
Acura is recalling 2014-2019 ILX vehicles because a deformed fuel tank may cause the fuel gauge to display inaccurate levels, potentially leading to stalling and crashes.
Kimberly-Clark is recalling U by Kotex Sleek Regular Tampons because they may come apart upon removal.
Spartan is recalling 2019-2020 K1 motor home chassis because missing or improper cotter pins may cause brake actuator rods to detach, increasing stopping distance.
Arthrex is recalling Nano Corkscrew FT Suture Anchors because they may break during insertion. The recall covers 1,418 units distributed in the US and abroad.
Forest River is recalling 2018 XLR recreational trailers because they lack liquid propane and carbon monoxide detectors, posing an injury risk.
Carrier is recalling ComfortPro 210STA and PC6112 auxiliary power units because a second power supply harness lacks a ground fault circuit interrupter, increasing injury risk.
Kimberly-Clark is recalling U by Kotex Sleek tampons because they may come apart upon removal. The recall covers 68,852,076 units distributed nationwide and in Canada.
Zimmer Biomet is recalling 971 Maximum Variable Pitch Compression Screw Caddies due to a potential for silicone shedding during cleaning and sterilization.
Kimberly-Clark is recalling U by Kotex Sleek Regular Tampons because they may come apart upon removal.
Zimmer Biomet is recalling 971 Maximum Variable Pitch Compression Tray Bases because they may shed silicone during cleaning and sterilization.
Meridian Bioscience is recalling Premier Cryptococcal Antigen kits because an enzyme reagent may not maintain stability, potentially causing false negative results.
Waldemar Link is recalling 11 LINK STEM Reconstruction Prostheses because a manufacturing defect prevents the reaming guide from reaching the intended depth, which may lead to incorrect surgical positioning.
Bayer Medical Care is recalling MAVIG Portegra and Portegra2 Overhead Counterpoise Systems because the head mount knob may not be properly tightened, causing the injector head to become loose or fall.
Kimberly-Clark is recalling U by Kotex Sleek Regular Tampons because the product may come apart upon removal.
Teva Pharmaceuticals USA is recalling specific lots of Olmesartan Medoxomil and Hydrochlorothiazide Tablets because they failed to meet dissolution specifications.
Arrow International Inc. is recalling specific lots of pediatric central venous catheters because the lidstock labels list incorrect priming volumes and flow rates.
Ethicon is recalling 840 units of PERMA-HAND Silk Sutures because the product inside the packaging does not match the size or type indicated on the label.
Bound Tree Medical is recalling 84 Curaplex Epi Safe Administration and Training Kits because the epinephrine vials inside expired in December 2018, despite the outer label showing January 2020.
Bound Tree Medical is recalling 747 Curaplex Epi Safe Kits because they are incorrectly labeled with an expiration date of May 2018 instead of May 2019, and the syringe component lacks 510(k) clearance.
Forest River is recalling 2017-2019 Glaval Entourage and Berkshire Coach Ultra motorhomes because a block heater cable defect may cause a fire.
Mack Trucks is recalling 2018 Anthem and Pinnacle vehicles because a clutch component may fail, causing unintended movement and increasing crash risk.