State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Walmart is recalling specific Hyper Tough 2 Ton Jack Stands that may collapse unexpectedly under load, posing a risk of injury to nearby persons.
ZF is recalling air bag crash sensors in 2019 Chrysler Jeep Cherokee and 2018 Volkswagen Atlas vehicles due to manufacturing defects that may delay or prevent air bag deployment.
Bio Source Naturals is recalling Wintergreen and Birch Sweet Essential Oils because the packaging is not child-resistant, posing a risk of poisoning to young children.
Miles Industries is recalling about 370 Valor H5 gas fireplaces in the U.S. because delayed ignition can shatter the glass window, posing burn and laceration risks.
General Motors is recalling 2020 Buick, Cadillac, Chevrolet, and GMC vehicles because the roof-rail air bag inflator may separate during deployment, increasing injury risk.
Xtreme Outdoors is recalling 2020 Little Guy Mini Max Trailers because understated weight ratings on certification labels may cause trailers to exceed tow vehicle capacity.
Transliquid Technologies is recalling Mystic Shield hand sanitizer bottles due to the presence of undeclared methanol.
Winnebago is recalling 2019-2020 Micro Minnie 5 travel trailers because a bedroom emergency exit window was not installed, potentially preventing escape during an emergency.
Lupin Pharmaceuticals is recalling Cefdinir for Oral Suspension due to out-of-specification assay results in retention samples.
Boston Scientific is recalling 48 IcePearl 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Carefusion 2200 Inc is recalling Thora-Para 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling IcePearl 2.0 CX 90 Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Medtronic Xomed is recalling IPC software upgrade v 2.7.3.0 because the M5 Microdebrider may rotate faster than the set value.
REV Recreation Group is recalling 2019-2020 Fleetwood Pace Arrow motorhomes because loose battery brackets may cause a short circuit and fire.
Carefusion 2200 Inc is recalling Safe-T-Centesis 6 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion 2200 Inc is recalling Safe-T 8 Fr Thora-Para Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion is recalling Safe-T PLUS Thora-Para 5 Fr Non-Valved Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling 79 IceFORCE 2.1 CX Prostate Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.
Boston Scientific is recalling 88 Prostate Cryoablation Kits because needle surfaces deteriorated during procedures due to unexpected electrolysis.
Carefusion 2200 Inc is recalling Safe-T 5 Fr Thora-Para Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion 2200 Inc is recalling Safe-T-Centesis PLUS 6 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion 2200 Inc is recalling Safe-T-Centesis PLUS 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling 193 IcePearl 2.1 CX Prostate Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.
Boston Scientific is recalling 205 IcePearl 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Philips is recalling 3,075 IntelliVue G7m Anesthesia Gas Modules due to a firmware issue that may interrupt gas measurement and display.