State
72,820 recalls have nationwide distribution and so reach Alaska. 1,763 additional recalls listed Alaska specifically in their distribution scope.
Of the 1,763 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 349 (20%) are Severe.
Which agencies issued them
These figures cover only the 1,763 recalls whose distribution notice names Alaska specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Louisville Ladder is recalling over 1.7 million attic stairway ladders because the bolts can break during use, creating a fall hazard. Eleven reports of bolt breakage have been received, including one injury.
Wnttmt-branded infant walkers are being recalled because they pose serious injury or death risks from falls and entrapment. These products were sold on Amazon by WURUI.BABY.
Fitueyes, Inc. is recalling Laziza Dressers because they pose tip-over and entrapment hazards that could cause serious injury or death to children.
International is recalling 2027 HV, HX, LT, MV, and RH trucks because a wiper nut may loosen, causing wipers to disconnect and reducing visibility.
Evenflo is recalling Revolve180 Litemax NXT child seats manufactured through March 31, 2025, because a miscalibrated level indicator may cause the seat to sit too upright, increasing injury risk in a crash.
KC Imports and Exports is recalling Laser & LED Light Mini Laser Pointer Keychains because button cell batteries can be easily accessed by children, posing a risk of serious injury or death.
OKK Trading, Inc. is recalling three models of Easter LED Headbands because the lithium coin batteries can be easily accessed by children, posing a risk of serious injury or death.
Mack Trucks is recalling 2027 Anthem and Pioneer models because center roof marker lights may fail to illuminate, reducing visibility.
Syera is recalling Space Astronaut LED Finger Lights sold on Temu because the button cell batteries can be easily accessed by children, posing a risk of serious injury or death if swallowed.
Volvo Trucks is recalling 2026-2027 VNL and VNR models because center roof marker lights may fail to illuminate, reducing visibility.
Toyota is recalling 2026 bZ Woodland vehicles equipped with a tow converter due to an electrical short circuit risk that can disable stability control and keep brake lights on.
Chrysler (FCA US, LLC) is recalling certain 2023-2026 Alfa Romeo Tonale and 2023-2025 Dodge Hornet vehicles because the rear outboard seat belts may fail to retract properly.
Toyota is recalling certain 2024 Tacoma hybrid and 2024-2025 Tacoma vehicles because their rear shock absorber assemblies may corrode and fail, potentially detaching the external oil reservoir and creating a road hazard.
Chrysler is recalling specific Mopar seat belt assemblies because the rear outboard belts may twist and fail to retract, increasing injury risk.
ResMed is recalling Astral 100/150 ventilators because supercapacitor electrolyte leakage can damage the charger chip, trigger a fail-safe state, and interrupt ventilation therapy.
Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula Model 77722 due to potential pinhole leaks in the wire-wound body during use.
Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula (Model 77522) due to potential pinhole leaks in the wire-wound body during use.
Windstone Medical Packaging is recalling 15 AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues reported by Elevaris Medical Devices Inc.
Stryker GmbH is recalling Stryker Hoffmann II Connecting Rod Micro 3 x 150mm due to the potential for the rods to crack following cleaning and sterilization processes.
Windstone Medical Packaging is recalling 465 AMS medical convenience kits in connection with a Medicom recall of Ritmed Neurological Sponges due to potential endotoxin level variability.
Philips is recalling certain CT scanners because the clinical scan may not start automatically after Bolus Tracking, which could require a patient rescan and expose them to additional radiation.
Instrumentation Laboratory is recalling Bar Code Reader (BCR) wands used with GEM Premier 5000 and 7000 systems because they may assign patient results to the wrong patient ID.
Mylan Pharmaceuticals is recalling one lot of Mycophenolate Mofetil for Injection, 500 mg/vial, because precipitate was found in the vials. The recall covers 5,688 vials distributed nationwide.
Medicom is recalling specific lots of Ritmed Neurological Sponges (Models 55992C to 55998C) because of potential unexpected variability in endotoxin levels.
Instrumentation Laboratory is recalling Bar Code Reader (BCR) wands used with GEM Premier 5000 and 7000 systems because they may assign patient results to the wrong patient ID.