State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Toshiba is recalling 165 Aquilion Lightning CT scanners because a reconstruction error may interrupt scanning if the scan range exceeds the maximum Field of View.
Integra LifeSciences Corp. is recalling specific lots of Lumbar Drainage Sets because final inspection revealed an incomplete packaging seal on the sterile product.
Ivoclar Vivadent is recalling 5 units of Zenostar MT Color Impulse orange dental porcelain due to potential packaging leaks that may cause skin irritation.
Ivoclar Vivadent is recalling 19 units of Zenostar MT Color C2 dental porcelain coloring liquid due to potential packaging leaks that may cause skin irritation.
Ivoclar Vivadent is recalling 7 units of Zenostar MT Color B4 dental porcelain liquid due to packaging leaks that may cause skin irritation.
Arrow International Inc is recalling 2,425 Walrus Arterial Embolectomy Catheters nationwide due to incorrect labeling.
Ivoclar Vivadent is recalling 25 units of Zenostar MT Color Impulse violet dental porcelain coloring due to packaging leaks that may cause skin irritation.
Ivoclar Vivadent is recalling 11 units of Zenostar MT Color A4 dental porcelain liquid due to potential packaging leaks that may cause skin irritation.
Sun Pharmaceutical Industries is recalling 31,762 bottles of Bupropion Hydrochloride Extended-Release Tablets because they failed dissolution specifications.
Philips Medical Systems is recalling 185 Brilliance 64 CT scanners because infant head scans in High Resolution mode may show degraded image quality.
Ivoclar Vivadent is recalling 60 units of Zenostar MT Color Impulse grey dental porcelain due to packaging leaks that may cause skin irritation.
Biocompatibles is recalling Varithena administration packs because they contain the incorrect type of syringe. The recall covers 3,254 packs distributed nationwide.
Terumo is recalling CDI H/S Cuvettes because they may fail to connect to the probe, causing the monitor to display an error and preventing blood parameter display.
Siemens is recalling RAPIDPoint 400 Measurement Cartridges because of an error in the value assignment for Chloride calibrators.
Siemens Healthcare Diagnostics is recalling RAPIDPoint 405 Measurement Cartridges due to an error in the value assignment for Chloride calibrators.
Shire is recalling 7,680 bottles of Vyvanse 30 mg capsules because foreign tablets or capsules were found in the product.
Hyundai is recalling 2015-2016 Sonata and Sonata Hybrid vehicles because the panoramic sunroof panel may detach while driving, creating a road hazard.
Nissan is recalling 2017 Versa vehicles because a seam in the side curtain air bags may tear during deployment, increasing the risk of injury in a crash.
Specialized is recalling about 1,000 road bicycles because the rear wheel can detach, causing frame fractures and potential rider injury.
Christianson is recalling aluminum black ladders for Toy Hauler RVs because the hinges may separate, causing the ladder to fall and risk injury.
Honda is recalling 2016 Civic vehicles because the electric parking brake may fail to engage immediately after the ignition is turned off, increasing the risk of the vehicle rolling away.
Silver Springs Farms is recalling ground beef and sandwich steak products that may be adulterated with E. coli O157:H7.
REV Ambulance Group is recalling 39 ambulances from 2016-2017 because defective seat tracks may allow attendant seats to move rapidly during a crash, increasing injury risk.
Newmar is recalling 2015 Dutch Star motorhomes because the brake signal to towed devices may not deactivate, causing dragging brakes, overheating, fire, or crashes.
Hyundai is recalling 2010-2016 Genesis Coupe vehicles because the front passenger air bag sensor connector may dislodge, potentially causing incorrect air bag deployment in a crash.