State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Transonic Systems Inc is recalling 2 mm Flow Probes due to programming errors causing incorrect meter readings.
Neuro Kinetics is recalling 45 I-Portal NOTC systems because the OVAR research test was sold with an incorrect investigational label.
Ortho-Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry Systems because a software anomaly may reset user-configured parameters to defaults during installation.
Beckman Coulter is recalling Access Thyroglobulin Assay reagent packs because some may exhibit greater than 10% imprecision at low concentrations.
Transonic Systems Inc is recalling 3 mm Flow Probes due to a software defect that causes flow meters to display incorrect status messages.
HoneyCombs Industries is recalling 262 bottles of Expello-C because the powdered golden seal ingredient contained coliform bacteria levels exceeding specifications.
Vintage Pharmaceuticals is recalling 8,705 bottles of Lisinopril 40 mg tablets because they failed dissolution specifications. The affected lots were distributed nationwide and in Puerto Rico.
Transonic Systems Inc is recalling 2 mm Flow Probes due to programming errors causing incorrect meter readings.
Transonic Systems Inc is recalling 6 mm Flow Probes due to programming errors causing incorrect meter readings.
Transonic Systems Inc is recalling 2 mm Flow Probes due to programming errors causing incorrect meter readings.
Transonic Systems Inc is recalling 4 mm Flow Probes due to software defects causing incorrect meter readings.
Transonic Systems Inc is recalling 3 mm Flow Probes due to software defects causing incorrect readings on flow meters.
HoneyCombs Industries is recalling 68 units of Formula L droppers due to coliform counts exceeding specifications.
HoneyCombs Industries is recalling 432 bottles of Golden Seal Extract because the product contained higher levels of coliform bacteria than allowed by specifications.
Transonic Systems Inc is recalling 8 mm Flow Probes due to a software defect that causes flow meters to display incorrect error messages.
HoneyCombs Industries is recalling 55 bottles of Formula IM because the powdered golden seal ingredient contained coliform bacteria levels above the specified limit.
Silarx Pharmaceuticals is recalling 576 bottles of Lamivudine Oral Solution because the expiration date on the carton does not match the bottle label.
Qualitest Pharmaceuticals is recalling 21,552 bottles of 300 mg Allopurinol tablets because some tablets are oversized and discolored.
Olli Salumeria Americana is recalling pork salami products because the packaging lacks an ingredient list, failing to disclose the presence of sulfites from wine.
Schrader Farms is recalling approximately 20 pounds of ground beef sold in Seneca County, New York, due to possible non-O157 E. coli contamination.
Cummins is recalling certain ISB6.7, ISL9, ISX12, and ISX15 engines because a faulty Engine Control Module may cause the engine to stall without warning, increasing crash risk.
Hyundai is recalling approximately 99,500 2009-2011 Accent vehicles because a malfunctioning brake light switch may prevent brake lights from illuminating or disable cruise control.
Rejuvenation is recalling about 780 Shaker chairs and bar stools because the legs and back can break, causing the user to fall.
Nestlé Waters North America is recalling about 190 water dispensers because screws holding the heat band can break, causing the unit to overheat and posing a fire hazard.
IKEA is recalling VYSSA SPELEVINK crib mattresses because they fail to meet federal flammability standards, posing a fire hazard. No injuries have been reported.