State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Philips is recalling infant/child defibrillator pads due to incorrect age range labeling on the foil packaging.
GE Healthcare is recalling Proteus XR/a radiographic systems because they may fail to provide an audible indication when an exposure is complete.
GN Otometrics is recalling Gold Cup and Snap Leadwires because the electrode lead connector has a protruding conductor beyond the insulation.
Smiths Medical is recalling Medfusion 4000 Syringe Infusion Pumps with PharmGuard Server Software due to potential wireless network connectivity issues caused by a Radio Module defect.
Johnson Matthey Inc. is recalling fentanyl citrate active pharmaceutical ingredient due to potential glass contamination.
Siemens Healthcare Diagnostics is recalling 169 kits of the Atellica IM anti-CCP IgG assay because a reagent carryover mitigation step fails to complete on the analyzer.
Roche Diabetes Care is recalling the Accu-Chek Connect App because users on Android OS 8.0 and above may be unable to transfer meter values to the app.
Akorn, Inc. is recalling Lidocaine Hydrochloride Jelly USP, 2% due to a finding of metal particulate matter in the filling room. No particulates were identified in the product itself.
Arrow International Inc is recalling 520 units of ARROW+gard Blue PSI Kit Cath-Gard central venous access devices because they may contain the incorrect banner card.
Pfizer is recalling 7,824 bottles of ethosuximide capsules because the expiration date on the label is incorrect.
Randox Laboratories is recalling Randox Urinalysis Control Level 2 kits because the leukocyte range for the Siemens Multistix method was incorrect.
Pfizer is recalling 7,686 bottles of Zarontin (ethosuximide) capsules because the expiration date on the label is incorrect.
BMW is recalling 2017-2020 K 1600 GT, GTL, and B motorcycles because transmission parts may not be hard enough, risking rear wheel lockup and crashes.
Jayco is recalling 2019-2020 Jay Feather X19H travel trailers because emergency exit window handles may not allow windows to open sufficiently for egress.
Jayco is recalling 2019-2020 Redhawk SE motorhomes because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition, increasing crash injury risk.
Ford is recalling 28,579 2019 F-250 and F-350 trucks because the passenger-side rear axle shaft may fail prematurely, potentially causing loss of drive power or unintended movement.
Keystone is recalling 2020 Cougar fifth wheels and travel trailers because incorrect solar wiring may cause an electrical short circuit and fire.
Ford is recalling 2020 Explorers because a wiring harness may contact the A/C pulley, causing a short circuit and increasing fire risk.
Tip Top Poultry is recalling ready-to-eat chicken products produced in 2019 due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Mercedes-Benz is recalling certain 2019-2020 A 220, CLA 250, and GLC 300 vehicles because the driver's front airbag module may not be properly secured.
Bombardier Recreational Products is recalling 2019-2020 Can-Am Ryker motorcycles because wheel nuts may crack, causing wheels to loosen and increasing crash risk.
Jaguar is recalling 2019-2020 F-Type vehicles with 18-inch rear wheels because the tire placard label lists an incorrect tire size, which could lead to improper tire installation.
BMW, Rolls-Royce, and Toyota are recalling specific 2018-2020 models because backup camera settings may persist, hiding the rear view image and increasing crash risk.
Daimler Trucks North America is recalling 618 school buses because loose torque converter fasteners could cause the vehicle to become disabled in traffic, increasing injury risk during evacuation.
Lucon is recalling 2018-2019 Custom Heavy Haul dual axle trailers because axle bearings may lack proper grease, increasing crash risk.