State
73,566 recalls have nationwide distribution and so reach Alaska. 1,766 additional recalls listed Alaska specifically in their distribution scope.
Of the 1,766 recalls naming Alaska we have scored against our rubric, 118 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 470 (27%) are Severe.
Which agencies issued them
These figures cover only the 1,766 recalls whose distribution notice names Alaska specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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.
Porsche is recalling 2021 Cayenne GTS vehicles due to engine cylinder bore cracks that may cause engine damage, stalling, or oil leaks, increasing the risk of a crash or fire. Dealers will replace the engine at no charge.
Gulf Stream is recalling certain 2021 travel trailers because the Federal Certification Label lists incorrect tire size and pressure information. Overinflated tires increase the risk of crashes.
Wild Republic is recalling slap watches because the coin cell batteries can fall out, posing ingestion and choking hazards to young children.
Audi is recalling five 2021 model vehicles for engine cylinder bore cracks that may cause engine damage, stalling, oil leaks, and increased fire risk.
Briggs & Stratton is recalling YTL, Longli, and TIYA log splitters with 250cc engines due to a kickback hazard that caused two broken wrists.
Airstream is recalling certain 2021 Interstate Nineteen motorhomes due to potentially incorrectly wired bus bar circuit breakers that may overheat and create a fire risk. Dealers will relabel and relocate the affected wires free of charge.
Airstream is recalling certain 2020 and 2021 Flying Cloud and International travel trailers because the stove was incorrectly installed in a non-sealed cabinet. Drafts can force flames into the cabinet, creating a fire hazard.
Medtronic is recalling 23 Abre Venous Self-expanding Sent Systems because the device size is incorrectly printed on the device itself, though the packaging is labeled correctly.
LeMaitre Vascular is recalling 616 LeverEdge Contrast Injectors because particulates in the packaging foam could contaminate the sterile field.
Oto Med Inc is recalling 415 SpineX Bone Dust Collectors because holes were found in the sterile Tyvek pouches during internal testing.