State
73,509 recalls have nationwide distribution and so reach Nebraska. 4,576 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,576 recalls naming Nebraska we have scored against our rubric, 715 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,343 (29%) are Severe.
Which agencies issued them
These figures cover only the 4,576 recalls whose distribution notice names Nebraska specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The Boppy Company is recalling approximately 3.3 million Boppy newborn loungers due to suffocation risk. Eight infant deaths have been reported associated with the product.
Braun Ambulances is recalling 2020-2021 Demers MXP153 vehicles because damaged electrical wires and oxygen tubes may increase fire risk.
Altec is recalling 2011-2016 AT200A aerial devices because cracks in the mounting frame legs may cause the side plate to break, increasing injury risk.
Volkswagen is recalling 2018 Tiguan vehicles because an incorrect roof reinforcement assembly may have been installed during prior repairs, potentially compromising structural integrity and airbag deployment.
Nissan is recalling 2022 Pathfinder vehicles because the third-row headrests may move or detach due to improper welds or misaligned components. Detached headrests could fail to restrain occupants in a crash, increasing injury risk.
DRV Suites is recalling 2018-2021 Elite and Mobile Suites because brake caliper clips may bend, causing the caliper to unseat and increasing crash risk.
Daimler Trucks North America is recalling 2015-2018 Thomas Built Minotour school buses because a corroded solenoid connector may cause an electrical short, leading to fire.
Nissan is recalling certain 2022 Pathfinder vehicles because the second-row seat back frames may have insufficient welds that could separate. This could cause seats to fail to restrain occupants properly during a crash, increasing injury risk.
Ready Pac Foods is recalling ready-to-eat salads containing meat and poultry because they include salad dressing with an undeclared anchovy allergen.
General Motors is recalling certain 2021 Chevrolet Tahoe vehicles due to a fuel pump power control module defect that may cause engine stalls, increasing crash risk.
Motor Coach Industries is recalling 2005-2012 MCI J4500 and E4500 motorcoaches because the wheelchair lift's outer barrier may fail under force, increasing injury risk.
Ducati is recalling 2019 Hypermotard 950 SP motorcycles because the side stand may be improperly welded. A broken stand could cause the motorcycle to fall, increasing injury risk.
Polaris is recalling about 13,000 model year 2011–2021 Phoenix 200 ATVs because the throttle speed control stop can break and become stuck, posing a crash hazard. The company has received 18 reports of throttle stop failure including one crash with minor injury.
Hydro Pineapple Burn Max Health supplement sachets are being recalled because they contain undeclared sibutramine and were marketed without FDA approval. The product was distributed nationwide.
Ford is recalling 2011-2013 Explorers in 23 states and D.C. because a rear suspension part may fracture, causing loss of steering control.
Cordis Corporation recalls SUPER TORQUE MB angiographic catheters worldwide due to risk of entrapment between endovascular devices and vessel wall, potentially causing marker band dislodgement.
Cordis is recalling its SUPER TORQUE MB Angiographic Catheter worldwide because it may become entrapped between endovascular devices and the vessel wall. This entrapment can cause marker band movement or dislodgement.
Armstrong Medical Services Limited is recalling AMSORB PLUS PREFILLED anesthesia canisters due to risk of high resistance to gas flow that could prevent adequate ventilation. Not all defective units will be detected by standard pre-use testing.
Greenpark Compounding Pharmacy is recalling Spironolactone Ophthalmic Solution 0.005 mg/mL due to lack of assurance of sterility. The 15 mL bottles were distributed nationwide.
ICU Medical Inc is recalling AMINOSYN II 15% An Amino Acid Injection due to the presence of particulate matter including fibers, hair, and proteinaceous material found in retained samples.
Florance Morris ANTISEPTIC Hand Sanitizer (70% ethyl alcohol) in 8.45 fl oz and 33.81 fl oz bottles is being recalled due to methanol contamination found in some lots. All lots are affected due to manufacturing under the same conditions as contaminated products.
Florance Morris ANTISEPTIC Hand Sanitizer (70% ethyl alcohol) distributed nationwide is recalled due to FDA-detected methanol contamination and insufficient ethanol content. The product was distributed by Asimex International LLC in Florida.
Teligent Pharma is recalling Lidocaine Hydrochloride Topical Solution, USP 4% due to the product being superpotent. The recall affects 32,544 bottles distributed nationwide in the United States and Canada.
Cordis is recalling approximately 1,610 SUPER TORQUE PIG PIGTAIL SPECIAL angiographic catheters worldwide because the device can become entrapped between endovascular devices and the vessel wall, potentially causing marker band movement or dislodgement.
Cordis is recalling angiographic catheters that may become entrapped between devices and vessel walls, risking marker band dislodgement during vascular procedures. Approximately 71,330 units were distributed worldwide.