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.
HVL, LLC is recalling Metabolic Cleanse Revised because the product labeling fails to declare the milk allergen.
HVL, LLC is recalling 1,635 units of Metabolic Cleanse Veg because the product labeling fails to declare a milk allergen. The product was distributed to numerous US states, Puerto Rico, Canada, and several international locations.
Hospira is recalling 69 LifeCare PCA 3 pumps due to a screw rotation error that stops infusion and triggers an alarm.
HVL, LLC is recalling Ultra Protein Vanilla because the product labeling does not declare the milk allergen.
Immune Tree is recalling specific colostrum capsule products because they contain an undeclared milk allergen. Consumers should stop using the affected items.
Immune Tree is recalling specific colostrum products because they contain undeclared milk, a major food allergen.
Smith & Nephew is recalling Renasys Sterile Transparent Film and related dressing kits because sterility seal integrity failures may compromise the sterile barrier.
Trimed Inc is recalling 30 units of SMTP-10 Semi-Tubular Plates because a non-locking screw passed through a plate hole during implantation.
Merge Healthcare is recalling CADstream software versions 4.1.3 and prior because an incorrect grid selection could lead to an incorrect biopsy or missed target during MRI analysis.
Newmar is recalling 2015-2017 Canyon Star recreational vehicles because the wheelchair access door may open while driving, increasing crash risk.
Immune Tree is recalling specific colostrum powder products because they contain undeclared milk, a major food allergen.
Immune Tree is recalling specific colostrum powder products because they contain undeclared milk, a major food allergen.
Sorin Group USA is recalling 5,264 Stöckert S5 Heart-Lung Machines worldwide due to a potential failure of the Uninterruptible Power Supply.
Ford is recalling 2013-2017 Focus hatchbacks with manual transmissions because the rear hatch may unlatch with a single button press, increasing injury risk.
Philips is recalling 394 HeartStart MRx Monitor/Defibrillators because the handle can separate from the housing due to broken mounts.
Kanan Enterprises is recalling Southern Grove Cashews with Sea Salt due to the possible presence of peanuts. The product was distributed in Ohio, Kansas, and Minnesota.
Immune Tree is recalling specific colostrum powder products because they contain undeclared milk, a major food allergen.
Abbott Medical Optics is recalling 84 SENSAR Foldable Intraocular Lenses because they were not checked prior to release, which may result in the release of mislabeled units.
Invivo Corporation is recalling 639 Philips Expression Information Portal (IP5) units because display numerics may freeze and menu keys may disable after extended run time.
McKesson Medical Imaging Group is recalling McKesson Radiology software versions 12.1.1 and 12.2 because the STAT priority icon was not displayed in the Study List when a study was opened.
Abbott Medical Optics is recalling 131 TECNIS OptiBlue intraocular lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Abbott Medical Optics is recalling 10 TECNIS Symfony intraocular lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Sun Pharmaceutical Industries is recalling specific lots of Carvediol Tablets because they failed impurity and degradation specifications.
Abbott Medical Optics is recalling SENSAR 1-Piece Intraocular Lenses because they were not checked prior to release, which may result in the release of mislabeled units.
Siemens Medical Solutions is recalling 338 Syngo.x PACS systems because a software error caused volume calculations for prostate and liver to be too high.