State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
FDA is recalling Castile soap towelettes in Foley trays and specimen kits due to bacterial contamination.
Nestle is recalling Stouffer's spinach souffle products due to the potential presence of glass pieces. Consumers should check their freezers for the specific production codes listed.
The FDA is recalling Castile soap towelettes included in Foley trays and specimen kits because they are contaminated with bacteria.
Aplicare Castile Soap towelettes included in Foley Trays and Mid stream specimen kits are being recalled because they are contaminated with bacteria.
Nidek Inc is recalling RT-5100 and RT-3100 refractors because the Near Point Chart Arm may lower spontaneously, posing a risk of slight injury to the patient's face or nose.
Covidien LLC is recalling Castile soap towelettes used in Foley trays and specimen kits because they are contaminated with bacteria.
FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits because they are contaminated with bacteria.
The FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.
FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.
Nestle is recalling specific DiGiorno, Lean Cuisine, and Stouffer's products due to the potential presence of glass pieces.
FDA is recalling specific lots of Castile soap towelettes used in medical kits due to bacterial contamination.
CareFusion is recalling 170 Alaris PC Unit Infusion Pump Model 8000 devices because a power supply component may cause system error codes.
Toshiba is recalling 28 DRAD-3000E FPD Wireless Systems because they fail to complete image transmission, resulting in no radiographic image.
King Henry's, Inc. is recalling Fruit & Nut Medley because it may contain undeclared FD&C Yellow #6. The recall covers 3,242 units distributed across 25 US states and British Columbia.
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Estradiol Test kits because the drug fulvestrant (Faslodex) may cause falsely elevated estradiol results.
Zimmer Spine is issuing a correction notice for the Universal Clamp System to provide updated cleaning and disinfecting instructions.
AstraZeneca is recalling Tudorza Pressair inhalers because some units have actuation counters set to a number other than 60.
Siemens Medical Solutions USA is recalling six syngo X Workplace medical workstations because imported segmentation results appear mirrored, rendering them unusable for ablation procedures.
Siemens is recalling ADVIA Centaur Enhance Estradiol tests because the drug fulvestrant may cause falsely elevated results.
Zimmer Biomet is issuing a correction notice to provide updated cleaning and disinfecting instructions for the Instinct Java System and Universal Clamp System.
Neurotherm, Inc. is recalling 135 curved radiofrequency cannulas because straight needles were incorrectly labeled as curved.
Forest River is recalling 2015-2017 Georgetown RVs because a vented window was installed instead of a required secondary egress window, posing a risk of entrapment.
Forest River is recalling 2013-2016 Puma recreational trailers because tires may contact the wheel well on bumps, risking tire damage and loss of control.
Terex is recalling 2011-2016 aerial devices because inadequate welds at the boom tip may cause the platform to tilt unexpectedly, increasing the risk of user injury.
CPSC reannounced the recall of Fiskars 32-inch bypass lopper shears after additional injuries were reported. Consumers should stop using the product and contact Fiskars for a free replacement.