State
73,827 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,822 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,486 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
phil&teds is recalling about 630 Dash v5 strollers in the U.S. because the folding hinge can become damaged, posing a pinch hazard to consumers.
FDA is recalling the Given Imaging Bravo pH capsule delivery device due to a potential allergic reaction risk for patients with nickel sensitivity.
Siemens is recalling Dimension Vista Triglyceride assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Hale Products is recalling Class 1 Ultraview Touchscreen Displays manufactured between September 2011 and May 2016. False switch activations may cause accessories to turn on or off, increasing crash risk.
Siemens Healthcare Diagnostics is recalling Dimension Assays: Triglycerides (TGL) because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Applied Medical Resources Corp is recalling Direct Drive Clip Applier CA090 units due to inconsistent clip application that may lead to unoccluded vessels.
Siemens is recalling ADVIA Chemistry Enzymatic Creatinine 2 reagents because N-Acetylcysteine and Metamizole can cause falsely depressed test results.
Siemens Healthcare Diagnostics is recalling the Advia Chemistry Assay: Direct HDL Cholesterol due to potential falsely depressed results caused by NAC or Metamizole interference.
Cummins is recalling specific ISX12 and ISX15 engines due to a potential Engine Control Module short circuit that may cause the engine to stall without warning.
Siemens Healthcare Diagnostics is recalling Dimension Enzymatic Creatinine assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Nuwati Herbals Inc. is recalling SeeLessO'Me Diet and Weight Management Tea because it contains undeclared soy. Consumers with soy allergies should not consume the product.
Siemens is recalling Dimension Vista Enzymatic Creatine assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Siemens Healthcare Diagnostics is recalling Advia Chemistry Assay: Lactate units because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Siemens Healthcare Diagnostics is recalling Dimension Uric Acid assays because N-Acetylcysteine and Metamizole can cause falsely low results.
Gillig is recalling 34 2016 Low Floor vehicles because the driver's side window may block too much light, reducing visibility and increasing crash risk.
Daimler Trucks North America is recalling 2,275 FCCC motorhome chassis due to a throttle sensor issue that may prevent the engine brake from activating, increasing crash risk.
Mobility Works is recalling 2014-2015 Ford and Chevrolet vans equipped with specific Ricon wheelchair lifts due to a risk of platform separation and injury.
Siemens Healthcare Diagnostics is recalling Advia Chemistry Assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Siemens is recalling ADVIA Chemistry Glucose Oxidase Assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Siemens Healthcare Diagnostics is recalling Direct HDL Cholesterol assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Mylan Pharmaceuticals is recalling 2,928 bottles of Paliperidone Extended-Release Tablets, 1.5 mg, because they failed dissolution specifications at a three-month stability time point.
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Triglycerides reagents because N-Acetylcysteine and Metamizole can cause falsely depressed test results.
Siemens Healthcare Diagnostics is recalling specific lots of Dimension Vista BUN Flex reagent cartridges because they may produce inaccurate patient or quality control results.
Baxter Healthcare is recalling 630 units of GEM FlowCoupler devices because the instructions for use booklet may puncture the outer Tyvek lid.
Baxter Healthcare is recalling 315 units of GEM Flowcoupler devices because the instructions for use booklet may puncture the outer Tyvek lid.