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.
School Specialty is recalling about 1,350 NeoRok stools because they can break during use, posing a fall hazard. No injuries have been reported.
Philips is recalling Q-Station ultrasound software because patient measurements may be incorrectly appended to other patients' studies.
Beaver-Visitec is recalling 214 ophthalmic procedure kits because the included Devon Light Gloves may have holes or slits that compromise sterility.
Dannmar is recalling MaxJax Portable Two-Post automatic car lift systems due to insufficient welding on lower carriage plates, which could cause the lift arms to snap and the vehicle to fall.
Roadtrek is recalling 335 model year 2014 motorhomes because electrical wiring under the front seats may damage, preventing the optional front thorax air bags from deploying in a crash.
Spartan Motors is recalling 2010-2015 Furion, Gladiator, and Metrostar emergency vehicles because the engine cooling fan may crack and detach, posing an injury risk to nearby individuals.
Neuro Kinetics is recalling 140 I-Portal NOTC and VNG devices due to system malfunctions and unintended sudden movements at startup. No injuries have been reported.
Ford is recalling 2014-2015 Escape and Transit Connect vehicles because a software issue may cause the instrument panel to stop working, potentially hiding safety warnings.
West-Ward Pharmaceutical Corp. is recalling Fentanyl Citrate Injection due to failed impurities and degradation specifications. The recall covers 14,649 cartons distributed nationwide.
Synthes, Inc. is recalling 54 units of 3.7mm Cannulated Locking and Conical Screws because certain lots were found to have been labeled incorrectly.
Allegiant Health is recalling specific lots of over-the-counter famotidine tablets because the manufacturer failed to adequately investigate customer complaints.
Dr. Reddy's Laboratories is recalling 5,160 bottles of Divalproex Sodium Extended-Release Tablets because they failed to meet dissolution specifications.
American Health Packaging is recalling 925 cartons of Lamivudine and Zidovudine Tablets USP 150mg/300mg because they failed dissolution specifications.
Dr. Reddy's Laboratories is recalling Divalproex Sodium Extended-Release Tablets because they failed to meet dissolution specifications at the 9-hour time point.
Amerx Health Care Corp. is recalling Amerigel Hydrogel Gauze Dressing 2 x 2 due to nonapproved labeling claims regarding sterility.
CooperSurgical is recalling 200 units of MILEX OMNIFLEX Diaphragms because size 80 boxes were incorrectly packaged with size 85 diaphragms.
Dr. Reddy's is voluntarily recalling specific lots of Amlodipine and Atorvastatin tablets because they contain less active ingredient than labeled.
Dr. Reddy's Laboratories is recalling specific lots of Amlodipine Besylate and Atorvastatin Calcium tablets because they contain less than the labeled amount of active ingredients.
Dr. Reddy's is recalling specific lots of Amlodipine and Atorvastatin tablets because they contain less active ingredient than labeled.
Dr. Reddy's Laboratories is voluntarily recalling specific lots of Amlodipine Besylate and Atorvastatin Calcium tablets because they contain less than the labeled amount of active ingredients.
Ohm Laboratories is recalling Loratadine Orally Disintegrating Tablets because an out-of-specification assay result indicated the drug was superpotent.
Ford is recalling 49 model year 2015 Transit vehicles because their seat belt labels are missing required model and year information, stating 'prototype sample' instead.
Altec is recalling 2013-2015 AH125, HL125, and AH150 aerial devices because rotation bearing fasteners may fail, posing a risk of injury or death.
Suzuki is recalling accessory backrest mounting hardware kits for 2006-2015 VZR1800 motorcycles because incorrect bolts may contact the rear tire, increasing crash risk.
Starcraft RV is recalling 50 model year 2014-2016 AR-ONE and Comet trailers because certification labels list the wrong tire size, which could lead to improper tire installation and increased crash risk.