State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pita Pal Foods LP is recalling PitaPal Hummus Variety Packs due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Aurolife Pharma is recalling 71,748 bottles of Member's Mark fexofenadine hydrochloride tablets because they failed impurity and degradation specifications.
Pita Pal Foods LP is recalling 7-Select Roasted Red Pepper Hummus with Pretzels due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Pita Pal Foods LP is recalling PitaPal Edamame Dip with Pretzels due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Pita Pal Foods LP is recalling specific lots of PitaPal Cilantro Jalapeno Hummus due to potential Listeria monocytogenes contamination. Consumers should check their products and discard them.
Pita Pal Foods LP is recalling specific lots of Roasted Red Pepper Hummus because the product may be contaminated with Listeria monocytogenes.
Aurolife Pharma is recalling 240 bottles of 180 mg Fexofenadine Hydrochloride tablets because they failed impurity and degradation specifications.
Pita Pal Foods LP is recalling Reasor's Roasted Red Pepper Hummus due to potential Listeria monocytogenes contamination.
Pita Pal Foods LP is recalling Reasor's Hummus Variety Pack 16 oz. due to potential contamination with Listeria monocytogenes.
Pita Pal Foods LP is recalling Schnuck's Roasted Red Pepper Hummus due to potential Listeria monocytogenes contamination.
Pita Pal Foods LP is recalling Lantana Cauliflower Hummus due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Ridge Properties, LLC is recalling Superior Pain & Itch Relief (lidocaine) Liquid Gel, 4%, because the product was found to be contaminated and above specification for lidocaine assay.
Pita Pal Foods LP is recalling Fresh Thyme Original Hummus with Pretzels because the product has the potential to be contaminated with Listeria monocytogenes.
Pita Pal Foods LP is recalling 840 cases of Roasted Garlic Hummus nationwide due to potential Listeria monocytogenes contamination.
Aurolife Pharma is recalling equate Allergy Relief tablets because they failed impurity and degradation specifications.
West-Ward Columbus Inc is recalling specific lots of Oxcarbazepine Oral Suspension because they failed impurity and degradation specifications.
Pita Pal Foods LP is recalling PitaPal Organic Cilantro Jalapeno Hummus due to potential Listeria monocytogenes contamination.
Wilson-Cook Medical Inc. is recalling 160 units of Hemospray Endoscopic Hemostat because misassembly may prevent the device from spraying powder.
Maquet is recalling 54 cardiopulmonary sets because quick connectors were assembled in reverse, preventing proper priming and function.
Volkswagen is recalling specific 2007-2019 models because internal evaluation modifications may cause non-compliance with regulatory requirements, potentially increasing crash risk.
Boston Scientific is recalling 404 EMBLEM MRI S-ICD devices because a compromised electrical component causes accelerated battery depletion, potentially requiring earlier replacement.
Boston Scientific is recalling 28 EMBLEM S-ICD devices due to accelerated battery depletion. Patients should contact their healthcare provider for evaluation.
Philips is recalling IntelliVue 1.4 GHz Remote Antenna cables used with MX40 monitors because they lack the required rating for some installations.
Torrent Pharma Inc. is recalling 2,472 bottles of Anagrelide Capsules because routine stability testing detected high levels of impurities.
Aurolife Pharma is recalling specific lots of 180 mg Fexofenadine Hydrochloride tablets because they failed impurity and degradation specifications.