State
73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Shyft Group is recalling 2021 Spartan K2 RV chassis because a rear suspension bracket may be improperly welded, increasing crash risk.
Prevost is recalling 2021 X3 Commuter Coaches because incorrectly assembled seat belts at flip-up seats may sit improperly on wheelchair users, increasing injury risk.
Leisure Time Products is recalling about 9,000 Brutus metal swing sets because the swing hanger attachment can fail, causing the swing to fall.
The Lye Guy is recalling sodium and potassium hydroxide products because the packaging is not child-resistant and labels violate federal hazardous substance requirements.
Freedman Seating Company is recalling GO-ES Double Flipseat and Double Rigid Seat models because the seat belt retractor may lock on inclines, increasing injury risk.
Polaris is recalling about 32 Model Year 2021 RZR PRO XP and RZR PRO XP 4 off-road vehicles because a missing copper seal washer can cause an oil leak and fire hazard.
Alliance Chemical is recalling sodium hydroxide products because the packaging is not child-resistant and labels violate federal hazardous substance laws.
General Motors is recalling 2019 Chevrolet 6500HD trucks because an engine software error allows speeds exceeding the tires' maximum rating, increasing crash risk.
Creative Foods Inc. is recalling Bueno Coffee Substitute Creamy Hazelnut because it contains undeclared hazelnut and peanut.
QMart is recalling Imperial Gold 2000 male sexual performance enhancement capsules because FDA analysis found undeclared tadalafil and/or sildenafil.
QMart is recalling PremierZen Extreme 3000 capsules because FDA analysis found unapproved drugs tadalafil and/or sildenafil.
Lamborghini is recalling 2021 Urus vehicles because cracks may develop on the engine cylinder bore, potentially causing engine damage, stalling, or oil leaks that increase the risk of a crash or fire.
Thule is recalling specific Tepui Hybox rooftop tents because the shell may crack at the mounting points, creating a road hazard.
Antoto-K is recalling Thumbs Up 7 Red 70K because FDA analysis found unapproved sildenafil and tadalafil. The product was marketed without an approved NDA or ANDA.
Forest Mushroom Food Inc. is recalling Guan's Enoki Mushroom because Michigan samples tested positive for Listeria monocytogenes.
Creative Foods Inc. is recalling Bueno Coffee Substitute Pecan Praline because it contains undeclared peanut and barley, posing a risk to individuals with allergies or celiac disease.
Equipment Technology, L.L.C. is recalling 87 aerial work platform vehicles due to inadequate welds that could cause the aerial unit to fail during use.
A-S Medication Solutions is recalling Health Essentials Kits containing Acetaminophen 500mg tablets. The bottles were incorrectly labeled with prescription drug labels instead of OTC labels.
QMart is recalling Burro en Primavera capsules because FDA analysis found unapproved tadalafil and/or sildenafil.
BMW is recalling 2021 230i and M240i vehicles because roof liner supports may detach and fall into the cabin, increasing injury risk during a crash.
ETI is recalling 2019-2020 ETC 37 IH vehicles because tilt cylinders may fail, causing unintentional bucket movement that increases injury risk.
QMart is recalling Imperial Platinum 2000 capsules because FDA analysis found unapproved ingredients tadalafil and/or sildenafil.
Greiner Bio-One is recalling VACUETTE blood collection tubes because insufficient draw volume may cause erroneous coagulation test results.
GE Healthcare is recalling 112 units of Centricity Universal Viewer software because a specific configuration may display comparison exams from the wrong patient.
Altec is recalling 2014-2021 TDA-58 aerial devices because transport tie-down chains may break, increasing crash risk.