State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Forest River is recalling specific 2016-2017 Berkshire and 2016 Cross Country recreational vehicles because front sway bar brackets may not fit properly, risking detachment and crashes.
CareFusion 303, Inc. is recalling 23,397 Alaris PC units, Model 8015, because a super capacitor failure may cause a system error code at power-up.
Applied Medical Technology Inc is recalling Wilson Penile Implantation System Retractor Frames due to a reported open pouch that breaches sterilization validation.
Great Lakes is recalling 1998-2016 Drywall Pup trailers because rear impact guards do not meet federal safety standards, increasing injury risk in crashes.
TwinGo is recalling about 4,000 baby carriers because the waist buckle can break, posing a fall hazard to children. No injuries have been reported.
Siemens is recalling eight MAGNETOM Aera/Skyra MRI systems because the patient table's docking station cover may contain a magnetic plate that attracts to the main magnet.
Applied Medical Technology Inc is recalling 1,100 units of the Wilson Implantation System after a complaint revealed an open pouch that breached sterilization validation.
Applied Medical Technology is recalling 3,754 units of TLC Self-Retaining Retractor Frames because a complaint reported an open pouch, which breaches sterilization validation.
Applied Medical Technology Inc is recalling 5,334 units of TLC Self Retaining Retractor Systems because a complaint reported an open pouch that breaches sterilization validation.
Ab Sciex is recalling Analyst MD software versions 1.6.1 and 1.6.2 because it may display wrong quantitative results, potentially leading to incorrect patient diagnoses.
Siemens is recalling 84 units of Syngo Dynamics software due to a defect that may cause old measurements to be carried forward into new reports.
Chrysler is recalling 2007-2010 Jeep Wrangler vehicles because dust contamination in the clockspring assembly may prevent the driver's air bag from deploying.
Pacific Coachworks is recalling 2016 Rage'N toy haulers because an incorrect Cargo Carrying Capacity value on the Federal Information label could lead to overloading.
Robert Bosch Tool Corp. is recalling about 91,000 Bosch 1380 Slim small angle grinders because they can overheat, melt brush covers, and expose hot components, posing a burn risk.
Iowa Select Herbs LLC is recalling 1-gallon bottles of Alcohol-Free Cyperus Leaf because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling 7.5 fl. oz. bottles of Cranberry because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Momordica Leaf under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Rhodiola Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Hawthorn Berry dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
Iowa Select Herbs LLC is recalling Yohimbe Bark products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Propolis (Ligustrum lucidum) supplements because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Jewel Weed under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Milk Thistle Seed products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Biosense Webster is recalling Pentaray NAV High-Density Mapping Catheters to clarify contraindication language regarding patients with prosthetic valves.
Alcon Research is recalling INFINITI Ultrasound Packs because the irrigation line tubing may leak near the white luer.