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.
A. L. Schutzman Company, Inc. is recalling Ashdon Farms Honey Mustard Mix because the packaging lists whey but fails to declare milk in the 'Contains' statement.
Zenobia Co. is recalling My Spice Sage Ground Flax Seed Meal due to the possible presence of Salmonella. The product was sold nationwide via the internet.
Hyundai is recalling 2011-2012 Elantra vehicles because an electronic stability control sensor malfunction may cause unexpected braking and reduced engine power, increasing crash risk.
Remel Inc is recalling specific lots of Gentamicin Antimicrobial Susceptibility Testing Discs because the antibiotic concentration may be insufficient, potentially leading to incorrect test results.
Chrysler is recalling 2015 Jeep Compass and Patriot vehicles because a power steering hose clamp may be installed incorrectly, increasing the risk of a fire.
Insulet Corporation is recalling 5,179 boxes of OmniPod Insulin Management Systems because the needle mechanism may fail to deploy or deploy with a delay.
A. L. Schutzman Company, Inc. is recalling Girl Scouts Honey Mustard Pretzel Mix because the product lists whey but fails to declare milk in the 'Contains' statement.
Insulet Corporation is recalling OmniPod Insulin Management Systems because the needle mechanism may fail to deploy or deploy with a delay.
GE Medical Systems is recalling 45 Optima IGS 320 systems due to a potential safety issue involving non-recoverable loss of displayed imaging.
Navistar is recalling certain 2007-2015 IC Bus transit models because wheelchair lift bearings may move out of position, causing the platform to fall.
H&H Trailers is recalling 1,847 model year 2015-2016 trailers because aluminum gate hinges may bend or break, potentially causing the gate to open unexpectedly.
Stryker is recalling 120 units of Guidewire Introducer Needles shipped after expiration or with minimal time remaining due to infection risk.
Verathon is recalling GlideScope Video Laryngoscope blades because silicone adhesive may fail, causing the blade halves to separate during use.
Honda is recalling specific VT750 motorcycles because a wiring defect may cause the engine to stall while riding, increasing crash risk.
bioMerieux, Inc. is recalling MYLA Clinic Patch 3.2.0 CD software because it may link test results to incorrect patient records when connected to specific laboratory systems.
bioMerieux is recalling MYLA Clinic Patch 3.3.0 software because it may link test results to incorrect patient records when connected to specific laboratory systems.
bioMerieux is recalling MYLA CLI software versions 3.x to 4.1 because it may link test results to incorrect patient records.
Beckman Coulter is recalling specific software versions for the DxH 600 and 800 Slidemaker Stainer systems because they allow the creation of multiple orders with the same specimen ID but different patient IDs.
GE Healthcare is recalling 108 Optima CL323i and Optima IGS 320 angiographic X-ray systems due to a potential loss of displayed imaging.
Forest River is recalling 2016 Prime Time recreational trailers because the Federal placard lists the wrong tire load range, which may lead to overinflation and tire failure.
Allied Recreation Group is recalling specific Holiday Rambler and Monaco motorhomes because a bolt on the electric entry steps may fracture, causing instability and injury risk.
bioMerieux is recalling MYLA software because it may link test results to the wrong patient record when connected to specific laboratory systems.
General Motors is recalling 2015 Chevrolet Cruze vehicles because a driver-side seat belt bolt may be loose. This defect could prevent the seat belt from holding in a crash.
Elekta is recalling MOSAIQ Oncology Information System versions prior to 2.60 because a third-party database update prevents the software from checking for drug-drug, drug-allergy, and duplicate therapy interactions.
Philips is recalling 105 Ingenuity Core CT scanners because software may set the scan length differently than planned during specific protocols.