State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Wohali Outdoors is recalling about 26,800 children's three-piece pajama sets sold at Bass Pro Shops because they fail federal flammability standards, posing a risk of burn injuries.
John Deere is recalling about 68,300 Crossover Gator utility vehicles because the steering shaft can separate, causing a loss of steering control and posing a crash hazard.
Walker is recalling 2018 Tank Trailers because improperly torqued brake caliper bolts may allow the caliper to detach, causing a loss of braking ability.
Wabash National is recalling 2018 Truck Body vehicles because a missing weld on the vertical leg support increases injury risk in rear-end collisions.
FCA US LLC is recalling 2018 Alfa Romeo Giulia and Stelvio vehicles because contaminated brake fluid may damage the braking system and reduce performance.
Sun Pharmaceutical Industries is recalling Riomet (metformin hydrochloride) oral solution due to microbial contamination. The recall covers specific lots of the cherry-flavored prescription liquid.
Physio-Control is recalling 14,219 LIFEPAK defibrillation electrodes because the artwork instructs incorrect pad placement and is missing required warning symbols.
Physio-Control is recalling 14,219 LIFEPAK Electrode Starter Kits because the infant artwork shows incorrect pad placement and is missing required warning symbols.
FCA is recalling specific Ram trucks because the brake transmission shift interlock pin may stick, allowing the vehicle to shift out of park without the brake pedal or key, increasing rollaway risk.
Navilyst Medical is recalling specific Xcela and BioFlo PICC kits because the included introducer sheath handles may detach during use.
Mobility Ventures is recalling 2011-2016 MV-1 vehicles because the driver's seat may disengage from the track during a rear impact, increasing injury risk.
Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included Greatbatch introducer sheaths have handles that may detach during use.
Navilyst Medical is recalling specific Xcela and BioFlo PICC kits because the included introducer sheaths have handles that may detach during use.
Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included introducer sheaths have handles that may detach during use.
Volkswagen Group of America is recalling 2018 Audi A5 Coupe vehicles because head curtain air bags may not unfold properly, increasing injury risk in crashes.
Eaton Cummins is recalling specific Endurant and PACCAR transmissions where the control module may allow the engine to crank if the shifter is not in neutral, increasing crash risk.
Toyota is recalling 2017-2018 models due to incorrect load carrying capacity labels that may lead to vehicle overloading and increased crash risk.
Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included introducer sheath handles may detach during use.
Navilyst Medical is recalling specific Xcela and BioFlo PICC kits because the included introducer sheaths may have handles that detach during use.
Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.
Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.
Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included introducer sheath handles may detach during use.
Terumo Medical Corp is recalling specific lots of Glidesheath Slender Introducer Sheaths because an incomplete seal may compromise sterility.
Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.
Elekta Inc is recalling 182 ERGO++ devices due to incorrect DICOM mapping of collimator or couch angles, which may lead to incorrect rotation during planning.