State
73,827 recalls have nationwide distribution and so reach American Samoa. 25 additional recalls listed American Samoa specifically in their distribution scope.
Of the 25 recalls naming American Samoa we have scored against our rubric, 1 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 9 (36%) are Severe.
Which agencies issued them
These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Atlas Spine, Inc. is recalling 16 Torque Limiting Handles because they were not appropriately set to mitigate the risk of implant fracture during rotation.
Siemens Healthcare Diagnostics is recalling Dimension Vista Uric Acid assays because NAC and Metamizole can cause falsely depressed results.
Medtronic is voluntarily recalling battery packs for the Capnostream 20 and 20p patient monitors because they may experience thermal runaway, posing a potential fire risk.
Heartland is recalling 2016-2017 Fair Field, Lakeview, and Resort trailers because safety chains may break if the main connection fails, increasing crash risk.
Stryker is recalling CinchLock Knotless Anchors after 13 reports of internal wire breakage upon deployment.
CVS Health is recalling Gold Emblem Abound Organic Spiced Herbal Tea because the product contains Salmonella. Consumers should stop using the product.
Lakota is recalling 2014 Luxe trailers because the built-in microwave may start on its own, posing a fire hazard.
Novarad Corporation is recalling specific versions of NovaPACS Diagnostic Viewer because the PET/CT fusion tool calculates incorrect SUV values.
Covidien LLC is recalling Bravo pH capsule delivery devices due to a potential risk of allergic reactions in patients with nickel sensitivity.
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.
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.