State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Rosenbauer America is recalling 2017-2018 Fire Apparatus vehicles because Whelen accessory brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Altec is recalling 2017-2018 Aerial Devices, Service Bodies, and Digger Derricks because Whelen accessory brake lights may illuminate without the brake pedal being pressed.
Keystone RV Company is recalling 2018-2019 Raptor recreational trailers because an incorrectly routed propane line allows the grill to be stored while lit, increasing fire risk.
Kawasaki is recalling 1,173 2018 Z900 and Z900RS motorcycles because the rear brake hose or sensor wire may contact the tire, risking brake failure or ABS malfunction.
Kawasaki is recalling about 1,000 Mule Pro off-highway utility vehicles because the rollover protection structure may fail to protect occupants, posing an injury hazard.
Meijer is recalling about 25,000 Falls Creek Kids infant and toddler hoodies because the zipper slider can detach, posing a choking hazard to young children.
Skip Hop is recalling Tuo convertible high chairs because the legs can detach from the seat, posing fall and injury hazards to children.
General Motors is recalling 2019 Chevrolet Silverado 1500 and GMC Sierra 1500 Crew Cab vehicles because the passenger-side air bag may not inflate properly in a crash.
NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.
Volkswagen is recalling 2018 Golf R vehicles because a fuel hose connector may detach, causing a leak that increases fire risk.
Eurotrol Inc. is recalling HemoTrol Level 2 hematology quality control mixtures because microbial contamination causes incorrect measurement results.
NxStage Medical is recalling 7,275 units of PureFlow B Solution because the bag's smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.
Synaptive Medical Inc is recalling 37 units of BrightMatter Guide software due to a defect that occurs when switching between specific port trajectories during surgery.
Volkswagen is recalling 2015-2016 Audi A6 and 2015 A7 vehicles because an incorrectly inserted auxiliary heater connector may overheat and cause a fire.
Maquet Cardiovascular is recalling QUADROX-i Neonatal membrane oxygenators due to a potential for blood leakage at the blood inlet connector when using a specific reducing screw adapter.
NxStage Medical is recalling specific lots of PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.
NxStage Medical is recalling PureFlow B Solution because the bag's smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.
Maquet is recalling QUADROX-i Neonatal membrane oxygenators because a specific reducing screw adapter may cause blood leakage at the inlet connector.
Volkswagen is recalling 2018 Audi A3 and TT models because a fuel hose connector may detach, causing a leak that increases fire risk.
Cummins is recalling ISV5.0 diesel engines because a slipping air compressor belt can reduce braking performance, increasing crash risk.
GE Healthcare is recalling approximately 182,640 Dash 5000 Patient Monitoring Systems because they may simultaneously restart during prolonged network overloads.
Ascend Laboratories is recalling Quetiapine 400 mg tablets because a metal shard was found in a tablet. Patients should stop using the affected lot and contact their healthcare provider.
GE Healthcare is recalling approximately 3,864 Solar 9500 Information Monitoring Systems because they may simultaneously restart if connected to the same network during a prolonged network overload.
GE Healthcare is recalling Solar 8000M patient monitors because they may restart simultaneously during network overload, potentially disrupting patient monitoring.
GE Healthcare is recalling approximately 73,673 Solar 8000i and 8000M patient monitoring systems because they may simultaneously restart during prolonged network overloads.