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.
Teleflex Medical is recalling 3,700 Rusch EasyCath Kits because they may not be sterile. The kits were distributed nationwide to eight states.
Burlington Medical is recalling 310 two-piece full wrap vests and kilts because the protective material may provide inadequate shielding against scatter radiation.
Inovo, Inc. is recalling 690 Single Luman Conservers because the pressure gauge may dislodge from the mount, creating a leak.
Seattle Manufacturing Corporation is recalling Kobah Ice Axes because the spike or head can detach from the handle, posing serious injury and fall risks.
Burlington Medical is recalling 210 thyroid collars because the protective material may provide inadequate protection against scatter radiation, potentially exposing users to increased health risks.
ImprimisRx NJ is voluntarily recalling 405 bottles of Timolol-Latanoprost P-F ophthalmic drops because the medication was found to be subpotent.
Burlington Medical is recalling 37 radiation protection kilts because the protective material may provide inadequate shielding against scatter radiation.
American Health Packaging is recalling Doxycycline Hyclate 100 mg tablets because they failed to meet dissolution specifications. The affected lot was distributed nationwide.
Agfa N.V. is recalling four DR 800 digital radiography systems because the exposed area of fluoroscopic exams may not match the active detector area.
Alto Development Corp is recalling Ultra-Flex MYO/Wire pacing wires to update instructions for use to ensure consistency with the M-21 loop electrode.
Lupin Pharmaceuticals is recalling Kaitlib Fe chewable tablets because long-term stability testing showed out-of-specification impurities or degradation.
Philips is recalling 229 Azurion Interventional Fluoroscopic X-ray Systems because a software defect may cause radiation levels too low for diagnostic images.
Major Pharmaceuticals is recalling 828 cartons of Divalproex Sodium Extended-Release Tablets because they were exposed to high humidity during packaging.
Piramal Critical Care is recalling Gablofen (baclofen injection) due to the presence of an unknown impurity observed during shelf life.
Xhale Assurance is recalling 701,272 Nasal Alar SpO2 Sensors because the Instructions for Use are missing steps for checking and changing the application site.
Ralston Group is recalling 534 Maximum Pelvic Trainer units because the device was incorrectly listed with the FDA and lacks a required 510(k) submission.
Altec Industries is recalling 2018-2019 aerial devices because high-strength fasteners may fail, potentially causing the pedestal to separate from the turntable.
BRP is expanding a recall for 2017-2018 Ski-Doo snowmobiles because the fuel delivery system can leak, posing a fire hazard. No injuries have been reported.
BMW is recalling 2008-2012 128i, 135i, and 135is vehicles because blower-regulator wiring may overheat and cause a fire. Owners should contact dealers for a free inspection and replacement.
KME is recalling specific 2018-2019 Predator fire trucks because front shocks may separate, potentially causing a loss of power steering assist and increasing crash risk.
Toyota is recalling 2019 RAV4 and RAV4 Hybrid vehicles because a damaged electrical connector may prevent the backup camera from activating, increasing crash risk.
Altec Industries is recalling 2017-2019 LS60 Aerial Devices because they may not meet stability requirements, creating a risk of overturning and injury.
Ford is recalling 2020 Explorer and Lincoln Aviator vehicles because a missing parking brake cover or Factory Mode setting may allow the vehicle to roll away or hide gear selection.
Harley-Davidson is recalling specific Touring and CVO Touring motorcycles because a luggage conversion kit removed rear red reflectors without providing replacements, reducing visibility.
Forest River is recalling 2019-2020 Arctic Wolf and Flagstaff trailers because incorrect pin box bolts may allow the hitch to rotate, increasing crash risk.