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.
Arcadia Trading Inc. is recalling 34 cartons of imported lizard fish found to be uneviscerated during FDA sampling.
Porsche is recalling specific replacement gasoline engines because screws may shear off, causing a fuel leak that increases the risk of fire.
Bard Peripheral Vascular is recalling Halo One 5F Introducer Sheaths due to complaints of sheath separation, kinking, and tip damage during use.
BioMerieux SA is recalling NucliSENS magnetic extraction reagents because a performance drift was observed in BK virus testing for certain silica batches.
Porsche is recalling 2017 911 and 718 models because fuel collection pipe screws may shear, causing a fuel leak that increases fire risk.
Country Home Products is recalling about 830 DR brand field and brush mowers because a fuel tank valve malfunction can cause gasoline release, posing fire and burn risks.
Advance Engineered is recalling 2014-2015 Dry Bulk Cargo Tank trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Fresenius Medical Care is recalling 2008T Series Hemodialysis Systems because a software error may cause the machine to execute a cancelled ultrafiltration rate instead of the displayed rate.
CareFusion is recalling Alaris Pump Modules and AIL sensor kits because false Air-in-Line alarms can interrupt medication infusions.
Bard Peripheral Vascular is recalling Halo One 5F Introducer Sheaths due to reports of sheath separation, kinking, and tip damage during use.
Bard Peripheral Vascular is recalling Halo One 5F Introducer Sheaths due to complaints of separation, kinking, and tip damage during use.
Fresenius Medical Care is recalling 2008K Series Hemodialysis Systems because a software error may cause the machine to execute a cancelled Ultrafiltration Rate setting.
BioMerieux SA is recalling 3,723 units of MagSIL (NucliSENS easyMAG Magnetic Silica) worldwide due to observed performance drift in BK virus testing.
Fresenius Medical Care is recalling 2008K@home hemodialysis systems because a software error may cause the machine to execute a cancelled ultrafiltration rate.
The Binding Site Group is recalling 129 Optilite Analyser units because the lid may fall suddenly and cause injury if not fully open.
Herr Foods is recalling Smoked Chipotle Flavored Kettle Cooked Potato Chips because the seasoning contains a milk ingredient with a potential risk of Salmonella contamination.
The Binding Site Group is recalling Freelite Human Lambda Free Kits due to a calibration curve change that causes an increase in false prozone flags.
Merge Healthcare is recalling Merge Cardio software versions 9.0 through 10.1.2 because a specific user action may cause images to be missing, potentially leading to incorrect diagnosis or treatment.
Great Basin Scientific is recalling the Staph ID/R Blood Culture Panel because the S. aureus probe could result in false positive results.
Herr Foods is recalling 2.0 oz. Chipotle flavored Kettle Potato Chips because the seasoning contains a milk ingredient with a potential risk of Salmonella contamination.
Meridian Bioscience is recalling Premier EHEC and Premier EHEC Bulk diagnostic kits because internal testing showed they can produce false positive results with some broth specimens.
UCI-FRAM is recalling FRAM Model G2 inline fuel filters because oversized connection hoses may cause fuel leaks, increasing fire risk.
Ultradent Products, Inc. is recalling NanoTips 30g dental tips because the stainless steel cannula may detach from the base, posing a risk during intra-oral procedures.
Fresenius Medical Care is recalling 2008K2 hemodialysis systems because a software error may cause the machine to execute a cancelled ultrafiltration rate instead of the displayed rate.
Shire PLC is recalling 4,520 bottles of Pentasa (mesalamine) 250 mg capsules because 500 mg capsules were found in the bottles.