State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Winnebago is recalling 2015-2017 Itasca and Winnebago recreational vehicles because a loose electrical connection may cause heat buildup and increase the risk of a fire.
Goodyear is recalling specific Dunlop SP50 tires manufactured between December 2012 and February 2014 because they may experience tread chunking, which increases the risk of a crash.
Mazda is recalling 2007-2012 CX-7 vehicles because water and salt may cause front suspension ball joints to corrode and separate, potentially leading to a loss of steering control.
Mazda is recalling 2009-2010 Mazda6 vehicles because moisture may damage the air bag control unit, preventing air bags from deploying in a crash.
General Motors is recalling 2016 Buick Verano vehicles because a misrouted fuel line may contact the engine, wear, and leak fuel, increasing the risk of a fire.
SpeeCo is recalling fence wire stretchers because a recoiling wire can strike bystanders, causing cuts and abrasions.
ACH Food Companies is recalling Durkee, Hy-Vee, and Food Club salad toppings because an ingredient may be contaminated with Listeria monocytogenes.
Tadano is recalling 2013-2015 all-terrain crane trucks because an improperly assembled air line connection may cause reduced braking or loss of mobility.
Zimmer Surgical Inc is recalling 90 units of Air Dermatome II Width Plates because the surface coating is blistering, peeling, and discoloring after use.
Draeger Medical is recalling Oxylog 3000 disposable pediatric patient circuits because isolated episodes of leakage were found at the check valve.
Honey Bunchie, LLC is voluntarily recalling Honey Bunchies Gourmet Honey Bars due to potential Listeria monocytogenes contamination in sunflower kernels.
Olympus Scientific Solutions Americas is recalling Analytical X-Ray Systems because the trigger lock may fail to prevent x-ray generation in test modes.
Temsa is recalling 2015-2017 TS45 motorcoaches because insufficient clearance between rear twin tires may cause them to rub and fail, increasing crash risk.
Michael's Naturopathic Programs is recalling Cholesterol Metabolism Factors tablets because they may contain undeclared milk and soy.
Chrysler is recalling 2016 Chrysler 200 vehicles because chassis fastener joints may not be tightened correctly, which could loosen and reduce steering capability.
Chrysler is recalling 2014-2016 Jeep Cherokee vehicles because seat fasteners may not be tightened correctly, increasing injury risk in a crash.
Let's Talk Health is recalling 417 bottles of Oxygen Nasal Wash because the product was marketed without FDA approval and does not comply with nasal decongestant monograph requirements.
Dennis East International is recalling whiskey glass and stone sets because the glass can break during use, posing a laceration risk.
Merge Healthcare is recalling 37 units of Merge HEMO software because the displayed International Normalized Ratio (INR) value does not match the imported value.
Philips is recalling UroDiagnost x-ray systems because bolts may break, causing the c-arm to move and sag.
Philips is recalling 993 MultiDiagnost Eleva x-ray systems because bolts attaching the clamping plate may break, causing the C-arm to sag.
Shocker Paintball is recalling RSX markers with blue main chambers because the part can unexpectedly eject from the rear, posing a risk of impact injury.
Stryker Medical is voluntarily recalling Spirit Plus hospital beds because broken actuators may cause the bed to lower unexpectedly, risking patient injury.
Philips is recalling 993 MultiDiagnost Eleva x-ray systems because bolts may break, causing the C-arm to sag. The recall covers units distributed worldwide.
Philips is recalling IntelliVue Patient Monitors because they may display outdated waveform data if powered on continuously for several months, failing to reflect current patient conditions.