State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kronos Foods is recalling Natural Mini Caterer's Assortment due to the potential for metal fragments in the baked goods.
Ameditech is recalling Micro Screen 6 Panel Cup drug abuse tests because they have shown reduced reactivity.
Kronos Foods is recalling its Deluxe Assortment baked goods due to the potential for metal fragments. The recall affects 8 cases distributed in specific US states and Canada.
Philips is recalling ECG sync cables used with HeartStart monitors because electrical interference can cause misinterpretation of heart signals or interrupt pacing.
Columbia Northwest is recalling 2013-2014 Somerset E1 and Santa Fe trailers because the water heater may overheat, causing scalding.
National Frozen Foods is recalling Target-exclusive Italian Blend frozen vegetables due to potential Listeria monocytogenes contamination.
National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Lakeside Foods is recalling specific lots of frozen peas and carrots after testing confirmed the presence of Listeria monocytogenes.
Forest River is recalling specific 2007-2015 motorhomes because a bolt on the electric entry steps may fracture, causing the steps to become unstable and increasing the risk of injury.
National Frozen Foods Corporation is recalling Monarch and Valmont Italian Vegetable Blend due to potential Listeria monocytogenes contamination.
Downing Labs, LLC is recalling Taurine Injectable, 50mg/mL, 30mL vials due to a lack of assurance of sterility. The recall affects 123 vials distributed nationwide and internationally.
Civco Medical Instruments is recalling 54 boxes of Large Gauge Infiniti Plus Needle Guides because the sterility of the product cannot be assured.
Kronos Foods is recalling Chocolate Almond Treasure because metal fragments were detected after increased metal detector rejections.
Kronos Foods is recalling Classic Baklava because metal fragments were detected during quality control. Consumers should stop eating the product and return it to the store.
Kronos Foods is recalling Orange Blossom Baklava due to the potential for metal fragments in the baked goods.
National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Civco Medical Instruments is recalling 717 boxes of Infiniti Plus Needle Guides because the sterility of the product cannot be assured.
Civco Medical Instruments is recalling 1,139 boxes of Biopsy Starter Kits because the sterility of the product cannot be assured.
Newmar is recalling 2016 King Aire vehicles that may lack a required emergency exit window over the driver's side dinette table, potentially delaying escape during an emergency.
US Compounding Inc is recalling 1,421 vials of Lincomycin/Lidocaine due to deficient practices that may impact sterility assurance.
TZ Medical Inc. is recalling Neptune Plus hemostasis pads because the instructions for use do not match the original FDA submission.
Vintage Pharmaceuticals is recalling 912 bottles of 12.5 mg Hydrochlorothiazide capsules because of the presence of particulate matter.
Ameditech is recalling specific Immutest drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and in Australia.
Ameditech is recalling 787 kits of 1 Step 12 Panel Cup drug tests due to reduced reactivity. The products were distributed in the US and Australia.
Astora is recalling 52 units of the MiniArc Pro Single incision Sling System because the lot number on the outer carton did not match the labels inside the box.