State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Crown Laboratories is recalling Nystatin Cream, USP, because the product failed potency testing at the 9-month interval.
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Calibrator lots 534177 and 534179 due to observed calibration errors in Total and Direct Bilirubin assays.
A.P. Deauville, LLC is recalling Soft Whisper Dandruff Shampoo because it was produced with water that failed USP specifications.
Argon Medical Devices is recalling BioPince Full Core Biopsy Instruments because of incorrect product labeling. The recall affects 165 units in the U.S. and 330 units internationally.
QuVa Pharma is recalling 17,050 syringes of R.E.C.K. solution because they may contain particulate matter. The product was distributed nationwide in the US.
Rising Pharmaceuticals is recalling Timolol Maleate Sterile Ophthalmic Solution due to a carton label mix-up where 0.25% bottles were shipped in 0.5% cartons.
American Health Packaging is recalling 265 cartons of Nabumetone Tablets because the carton label did not include the required statement to dispense with the accompanying Medication Guide.
Rising Pharmaceuticals is recalling 15,072 bottles of Timolol Maleate 0.25% ophthalmic solution because some outer cartons were mislabeled as 0.5% strength.
Utak Laboratories is recalling 1,395 vials of NR Trace Elements Serum Control due to incorrect cadmium reference values and expected ranges.
Pfizer is recalling Duavee tablets because they failed to meet dissolution specifications. The recall covers 544,400 packages distributed nationwide.
Volvo is recalling specific 2007-2020 models because a front seat belt cable may fatigue and fail to secure occupants during a crash.
Bridgestone is recalling specific V-Steel tires for mobile cranes because they lack required DOT and safety markings, potentially leading to unsafe operating conditions.
BMW is recalling 2020-2021 7 Series vehicles because the rear middle child seat tether anchor may be inaccessible, increasing injury risk in crashes.
Forest River is recalling 2021 Palomino Columbus recreational trailers because improperly located furnace vents may allow exhaust fumes to enter the trailer, posing a risk of carbon monoxide poisoning.
Forest River is recalling 2020-2021 Rockwood trailers with incorrect Gross Axle Weight Rating information on their Federal Placards. This could allow operators to unknowingly overload the vehicle, increasing crash risk.
Forest River is recalling the 2021 Cherokee Wolf Pack toyhauler because the propane line may be routed around sharp edges, which can cause a leak and fire risk. Owners should contact Forest River at 1-260-499-2100 for a free repair.
Chrysler is recalling 2020 Ram 1500 pickups and Promaster vans because a side curtain airbag diffuser may detach, preventing proper inflation in a crash.
FCA US LLC is recalling specific MOPAR steering drag link assemblies for Heavy Duty Ram 2500 and 3500 trucks because a jam nut may loosen, risking loss of steering control.
Tenneco is recalling Clevite-Pullman rear suspension lower control rods installed in Gillig Low Floor buses because the design makes them susceptible to failure over time.
Costway is recalling about 16,000 double baby strollers because they violate federal safety standards, posing fall, entrapment, and strangulation risks to children.
Apotex Inc. is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels.
Triple E is recalling 2020 Wonder W24MB, W24RTB, and W24FTB motorhomes because an improperly tightened electrical connection may short circuit and cause a fire.
GE Healthcare is recalling Giraffe OmniBed infant incubators equipped with Servo Oxygen modules because they may deliver a different oxygen level than displayed.
AvKARE Inc. is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Defibtech is recalling 860 Lifeline PRO AEDs because a component issue may cause the device to abort or fail to deliver a shock.