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.
Jayco is recalling 2019 White Hawk recreational trailers because screws securing ladder steps may break, posing a fall risk.
Jayco is recalling 2018-2019 Alante, Precept, Seneca, Redhawk, and Melbourne motorhomes because the cargo capacity label overstates limits, increasing crash risk.
Jayco is recalling 2019 Alante and Precept motorhomes because windshield wiper arms may lift at highway speeds, reducing visibility and increasing crash risk.
Keystone RV Company is recalling 2018-2019 Dutchmen Aerolite recreational trailers because the Federal Certification Label lists the wrong rim size, which could lead to unsafe rim replacements.
Philips is recalling 477 OmniDiagnost Classic X-ray systems because a broken tilt actuator could cause the table to rotate uncontrollably, posing a risk of injury.
Konica Minolta is recalling CS-7 medical devices because the Panasonic Toughbook laptops used in some configurations have a potential battery ignition risk.
Konica Minolta is recalling ImagePilot D9MA units because the Panasonic Toughbook laptops used in some configurations may experience battery ignition.
Philips is recalling 508 OmniDiagnost-Eleva X-ray systems because a broken actuator fixation can cause the table to rotate uncontrollably, posing a risk of injury.
St Jude Medical is recalling Promote Quadra implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
St Jude Medical is recalling Fortify ICDs and CRT-Ds to release new firmware that strengthens security against unauthorized access. Older devices may require permanent disabling of RF communication.
Teleflex Medical Europe Ltd is recalling 573 units of Pilling Universal Shears because incorrect plastic was used for the handles, causing them to melt during sterilization.
Siemens is recalling Artis zee MP systems because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.
St Jude Medical is releasing new firmware for high voltage implantable cardiac devices to strengthen security against unauthorized access.
Siemens Medical Solutions is recalling two Artis Q.zen biplane systems because the display may fail to show images after power save mode, potentially requiring treatment cancellation or patient transfer.
Siemens is recalling 39 ARTIS Pheno Interventional Fluoroscopic X-Ray Systems because the C-arm may drop up to 20 mm, potentially injuring patients.
Siemens Medical Solutions is recalling five Artis Q ceiling units because the display may fail to show an image after exiting power save mode, potentially requiring treatment cancellation.
Siemens Medical Solutions is recalling 56 Artis zeego systems because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Siemens is recalling 68 Artis zee biplane systems because the large display may remain black after exiting power save mode, potentially requiring treatment cancellation or patient transfer.
Cenorin, LLC is recalling 14 HLD Systems 600 Series Washer/Pasteurizers because a supplier quality issue with terminal blocks may cause overheating, charring, or burning.
St Jude Medical is recalling Unify Assura implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
St Jude Medical is recalling 68,117 Quadra Assura MP implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
St Jude Medical is recalling 72,673 Quadra Assura implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
St Jude Medical is recalling Unify Quadra implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Siemens is recalling Artis zee floor MN systems because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
RaySearch Laboratories is recalling RayStation Radiation Therapy Treatment Planning System software versions 6.0 through 7.0 because dose calculation accuracy may be less than expected in some situations.