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.
Volkswagen and Audi are recalling 2018 models because brake caliper pistons may have insufficient coating, potentially reducing braking performance and increasing crash risk.
Jayco is recalling 2018-2019 fifth-wheel trailers because the propane tank strap may separate, increasing the risk of a crash or fire.
Kia is recalling 507,587 vehicles because the air bag control unit may short circuit, preventing frontal air bags and seat belt pretensioners from deploying in a crash.
Starcraft is recalling 2019 Telluride fifth-wheel trailers because the propane tank strap may separate, increasing the risk of a crash or fire.
MORryde is recalling 2018 Ford E-450 chassis modified for transit bus use because insufficiently tightened U-bolts may allow the rear axle to separate, increasing crash risk.
PACCAR is recalling 2015-2018 Peterbilt and Kenworth trucks because the ABS warning light may fail to illuminate if power is lost, increasing crash risk.
General Motors is recalling 2019 Chevrolet Corvette ZR1 vehicles because the sensing diagnostic module may fail to deploy air bags in a crash.
Dorman is recalling specific front control arms where a ball stud may pull through the steering knuckle, causing partial loss of steering.
General Motors is recalling specific 2015-2018 GMC, Chevrolet, Buick, and Cadillac vehicles because a fuel pump may detach and cause a leak, increasing fire risk.
PACCAR is recalling 2019 Kenworth T270 and T370 vehicles because over-tightened rear axle nuts may cause bearing failure or fire, increasing crash risk.
Yakima is recalling HoldUp Evo hitch-mounted bike racks because the rear tire tray may separate while driving, increasing crash risk.
Ruiz Food Products is recalling 12-count frozen breakfast burritos that may contain white, semi-rigid plastic pieces. No adverse reactions have been reported.
The FDA is recalling Rhino 69 Extreme 50000 capsules because they contain undeclared tadalafil, an unapproved drug with unestablished safety and efficacy.
Nature's Only Choice is recalling B17 Bitter Raw Apricot Extract Amygdalin dietary supplements because the product is considered an unapproved new drug.
Ideaz Llc is recalling Screamin' Menthol Pain Relieving Gel because it contains benzene levels exceeding FDA limits.
Ideaz LLC is recalling Screamin' Hot Pain Relieving Gel because it was manufactured with benzene levels exceeding FDA limits.
Mylan Institutional, Inc. is recalling Loxapine Capsules 25 mg due to cGMP violations that create a risk of cross-contamination.
Nissan is recalling 2018 Infiniti QX30 vehicles because the right-hand lower seat belt anchorage bolt may be incorrectly installed, increasing injury risk in a crash.
Philips is recalling HeartStart FRx AEDs because a resistor issue may prevent the device from delivering a shock when needed.
Philips is recalling HeartStart AEDs because a resistor issue may prevent the device from delivering a shock when needed.
Smith & Nephew is recalling 13 units of Anthology hip prosthesis stems because they were manufactured with an undersized taper length.
Synthes (USA) Products LLC is recalling 50 Torque Limiting Handles because high-carbon ball bearings may rust prematurely, causing functional degradation.
Forest River is recalling 2019 Coachmen and Shasta recreational trailers because the liquid propane gas bottle ring may not bind the metal strap securely, risking bottle detachment.
Implant Direct Sybron Manufacturing is recalling 298 dental implants because the vial cap may display an incorrect part number, though the main label is correct.
Mylan Institutional, Inc. is recalling Loxapine Capsules 50 mg due to cGMP violations that create a risk of cross-contamination.