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.
The Children's Place is recalling about 14,900 infant snowsuits because metal snaps can detach, posing a choking hazard to young children.
Triple E is recalling 2019 Serenity recreational vehicles because a metal cable may contact the battery terminal, creating a fire hazard.
Volkswagen is recalling 2018 Audi A5 Sportback vehicles because front suspension fasteners may not be sufficiently tightened, which could cause a front wheel to become loose.
Heartland is recalling 2019 Milestone trailers because a propane hose may be improperly secured, posing a fire risk if it contacts the tire.
Blue Bird is recalling 2017-2019 Vision school buses with specific Cummins engines because a slipping air compressor belt may cause the parking brake to apply while driving, increasing crash risk.
Mannarich Food, Inc. is recalling approximately 145,245 pounds of Siluriformes fish products that were imported from Malaysia without U.S. inspection.
Autocar is recalling 2019 Xpeditor vehicles because universal joint strap bolts may not be properly tightened, which could cause the drive shaft to detach and increase crash risk.
Hyundai is recalling 2018 Elantra GT vehicles because the panoramic sunroof motor may be incorrectly programmed, preventing it from detecting obstacles while closing.
TAP Worldwide is recalling Poison Spyder Tire Carrier Delete Plates because they may interfere with brake lights and rear visibility systems, increasing crash risk.
Toyota is recalling 2018-2019 Tacoma vehicles because improper machining of the brake master cylinder may damage internal seals, potentially reducing brake performance and increasing crash risk.
Toyota is recalling 2008-2019 Land Cruiser and Lexus LX 570 vehicles because a broken wire harness may deactivate front passenger air bags, increasing injury risk in crashes.
Lifeworks is recalling specific Armor All heated seat cushions and blankets sold at Meijer because they may overheat and melt, posing a fire and injury risk.
TJX is recalling glass and ceramic drawer knobs sold at T.J. Maxx, Marshalls, and HomeGoods because they can shatter when pulled, posing a laceration hazard.
Lotus Foods is recalling rice ramen noodle soup cups because their labels incorrectly instruct consumers to use a microwave, posing fire and burn risks.
Frazer is recalling 2017-2018 Type 1 and Type 3 ambulances and Mobile Stroke Units because Whelen accessory brake lights may illuminate without the brake pedal being pressed.
The Company Store is recalling about 13,000 children's robes because they fail to meet federal flammability standards, posing a risk of burn injuries.
Raj Imports is recalling about 300 women's silk scarves because they fail to meet federal flammability standards, posing a risk of burn injuries.
Fresenius Kabi is recalling 1,312,350 vials of Sodium Chloride Injection because labels incorrectly state the stoppers do not contain natural rubber latex.
Toyota, Lexus, and Pontiac are recalling specific 2002-2007 vehicles because passenger air bag inflators may explode during deployment, posing a risk of serious injury.
Zimmer Biomet is recalling 8,027 Humeral Guide Wires because creases in the sealing area may compromise product sterility.
Invacare is recalling 73,703 hydraulic patient lifts because a mounting bolt may loosen, causing the caster to separate and the lift to tilt.
GE Healthcare is recalling CARESCAPE R860 Inspiratory Safety Guards because they may disconnect from the breathing circuit, potentially causing loss of ventilation and hypoxia in patients.
Philips is recalling 6,343 Brilliance 40 CT systems nationwide due to a potential fiberglass resin separation that could cause the gantry front cover to fall.
Fresenius Kabi is recalling 23.7 million sodium chloride vials because labels incorrectly state the stoppers do not contain natural rubber latex.
Agropur MSI Ingredients LLC is recalling Jay Robb Unflavored Egg White Protein due to undeclared milk. The recall covers 1,956 pouches distributed nationwide.