State
73,096 recalls have nationwide distribution and so reach Alaska. 1,765 additional recalls listed Alaska specifically in their distribution scope.
Of the 1,765 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 350 (20%) are Severe.
Which agencies issued them
These figures cover only the 1,765 recalls whose distribution notice names Alaska specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling certain 2020-2023 Pacifica and Voyager vehicles because an improperly secured side curtain airbag connector may prevent the airbags from deploying.
Nissan is recalling certain 2023-2024 Z vehicles because right-side pedestrian detection sensor connectors may be reversed, preventing the pop-up engine hood from activating.
GM is recalling certain 2025 Cadillac XT4 vehicles because the instrument panel may be missing the perforation that allows the passenger-side airbag to deploy properly.
Orange EV is recalling 2017-2024 T-Series and 2023-2024 e-TRIEVER trucks because manuals incorrectly describe the high-voltage lockout procedure, posing an electrical shock risk.
Spartan Fire is recalling 2024-2025 fire trucks because a missing mechanical stop may allow the cab tilt cylinder to overextend, potentially causing the cab to drop.
Chrysler is recalling 2025 Ram 1500 vehicles because damaged front wheel hub encoder rings can disable the electronic stability control system, increasing crash risk.
PowerBlock is recalling about 1,845 Commercial Pro 100 weight sets sold with 5 lb grip handles because weight plates above 55 lbs can dislodge during use, posing an impact injury risk.
Bionpharma Inc. is recalling Atovaquone Oral Suspension (750 mg/5 mL) nationwide due to Cohnella bacteria contamination. The recall affects 1,980 bottles.
Newmar is recalling 2023-2025 Super Star motorhomes because damaged inner tire valve extensions can cause tire failure and increase crash risk.
Silver Eagle is recalling specific eye and shank assemblies because welds may crack, allowing the eye to separate from the trailer converter dolly and increasing crash risk.
Volvo is recalling 2020 hybrid models because a loose brake pedal screw may cause loss of braking function, increasing crash risk.
Wilson-Cook Medical is recalling specific lots of Hemo-7 and Hemo-10 Hemospray Endoscopic Hemostats because they were manufactured with nonconforming raw materials.
Kinova Inc is recalling 949 KINOVA Jaco assistive robots due to a potential fire hazard that may occur if a damaged robot arm interacts with a wheelchair exhibiting electrical leakage.
Breckenridge Pharmaceutical is recalling 7,107 bottles of Duloxetine 20mg delayed-release capsules nationwide due to N-nitroso-duloxetine impurity exceeding FDA interim limits. No illnesses have been reported.
Leica cryostat units lack a warning about flammable freezing sprays that can ignite in the chamber. The company discovered through post-market surveillance that users were applying these flammable sprays without being warned of the fire hazard.
BlueFIRE Inflation Devices may have a small hole in the sterile barrier, potentially exposing patients to pathogens that could cause infection. Contact your healthcare provider if you received this device.
Mack is recalling certain 2020-2025 trucks with Bendix EC80 Advanced Electronic Control Units because electrical noise may cause the ECU to misprocess commands or stop working.
A software anomaly in the Boston Scientific AVVIGO+ Multi-Modality Guidance System causes an incorrect grid overlay display when used with certain catheters. The wrong overlay may lead to incorrect measurement references during imaging procedures.
Boston Scientific is recalling AVVIGO+ Multi-Modality Guidance Systems due to a software anomaly that displays a 9-grid overlay instead of the correct 15-grid overlay during Live and Record modes. This incorrect display could affect imaging measurements during procedures.
Merit Medical Systems is recalling Custom Inflation Kits due to a small hole in the sterile barrier that could expose users to pathogens and pyrogens, increasing infection risk.
Leica Biosystems Cryostat Model CM1510 S is recalled due to missing warning labels about flammable freezing sprays, which can ignite and cause serious injury. The device labeling lacked fire hazard warnings prior to 2019.
Boston Scientific is recalling AVVIGO+ systems due to a software anomaly that displays an incorrect grid overlay when connected to OptiCross 18 catheters, potentially leading to vessel imaging misinterpretation.
Hydration Labs Inc. is recalling Flavor#115 Electrolytes (3.78L BIB units) distributed nationwide and in Canada because the product is labeled as electrolytes but actually contains caffeine.
Merit Medical Systems is recalling approximately 6,565 Monarch Inflation Devices due to manufacturing defects that compromise the sterile barrier, potentially allowing device contamination.
Leica Biosystems is recalling Cryostat Model CM1850 (322 units, US nationwide) due to missing warnings about fire hazard from flammable freezing sprays. The device's labeling prior to 2019 did not warn users that flammable sprays used in the chamber can ignite and cause serious injuries.