State
72,913 recalls have nationwide distribution and so reach Alaska. 1,764 additional recalls listed Alaska specifically in their distribution scope.
Of the 1,764 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 1,764 recalls whose distribution notice names Alaska specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Aniara Diagnostica LLC is recalling ZYMUTEST HIA IgG diagnostic kits (Lot FD1265) due to an outdated flyer containing incorrect positive control values that could affect test result interpretation.
GE Medical Systems is recalling Revolution CT ES and related CT systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link based CT Smart Subscription. The vulnerability may affect system security.
Integra LifeSciences is recalling Codman CerebroFlo EVD Catheters (Lot 45322) because endotoxin levels did not meet acceptance criteria. The product was distributed nationwide.
GE HealthCare is recalling Revolution Apex Plus X-ray CT systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link. Eleven units are affected worldwide.
Hologic is recalling certain 3DIMENSIONS MAMMOGRAPHY SYSTEM models due to internal bolts that may become loose, missing, or broken over time. The FDA classified this as a Class II recall.
Stryker Corporation is recalling the Thermedx FluidSmart Urology Tube Set (Catalog No. LL0006) due to nonconforming products that were inadvertently distributed. The affected tube sets were distributed nationwide in Georgia.
DJO, LLC is recalling the DONJOY IceMan CLASSIC3 cold therapy unit (Model 11-1422) due to a broken connector that may interrupt prescribed cold therapy treatment.
Jolife AB is recalling 153 LUCAS chest compression systems (Models 2, 3, and 3.1) due to incomplete service documentation. Service work performed on affected systems was not properly documented in service records.
Ascend Laboratories is recalling 17,304 bottles of Metoprolol Succinate Extended-Release 25 mg tablets (Lot #25140859, expiring Jan 2027) distributed nationwide because the tablets failed dissolution specifications, which may affect drug effectiveness.
Jerr-Dan is recalling XLP Carrier kits because reverse and brake light assemblies may be installed incorrectly, reducing vehicle visibility and increasing crash risk.
Hyundai is recalling certain 2025 Ioniq 5 and 2026 Ioniq 9 vehicles because the rear suspension fasteners may loosen and detach, which can cause a loss of vehicle control.
Hyundai is recalling certain 2025 and 2026 Tucson, Tucson Hybrid, Tucson PHEV, and Santa Cruz vehicles due to front camera software that may cause the forward collision avoidance system to activate prematurely and unexpectedly apply the brakes, increasing crash risk.
Endera is recalling 2025-2026 Shuttle buses because wheelchair retractors may fail to lock, increasing injury risk.
Oshkosh is recalling 2025 NGDV electric vehicles because the high-voltage battery contactor may open unexpectedly in cold weather, causing a loss of drive power.
Keystone RV Company is recalling certain 2024–2026 recreational trailers because shock bolts may have been incorrectly tightened, which could cause loss of vehicle stability and increase crash risk.
Tesla is recalling certain 2025 and 2026 Model Y vehicles because the certification label may not have been installed. Missing weight information on the label could lead to vehicle overloading and increase crash risk.
Altec is recalling specific aerial device vehicles because the ground-level emergency stop may fail to halt hydraulic functions in ePTO mode, increasing injury risk.
Tiyol Pull String Teething Toys sold on Amazon are recalled due to oversized silicone strings that can lodge in the throat, posing a choking hazard. CPSC is aware of 11 choking incidents.
Minka Lighting Group is recalling about 170 Bardon Series Pendant Light Fixtures because the frame can detach from the downrod during installation, posing a risk of serious injury or death. One detachment has been reported with no injuries yet.
Missry Associates is recalling Misco Sports Badminton Toy Sets because the shuttlecocks contain button cell batteries that children can easily access and swallow, potentially causing serious internal injuries or death.
BRP US Inc. recalls about 2,820 Can-Am Outlander Pro and Max Pro ATVs with defective Speed Limiter Mode that can cause unexpected speed and acceleration, posing a risk of serious injury or death from crashes.
Cosyland Children's Tower Stools can collapse, tip over, or trap a child's torso through front and back openings, posing risks of serious injury and death. The firm is aware of 25 reports of stability issues and falls, with eight injuries including a fractured arm.
World Bright International Limited recalls Agio Menlo Woven Patio Swings (Model 1934256) sold at Costco because the swing seat can detach during use, risking serious injury or death. Eight injuries have been reported.
Hyundai is recalling 2015-2016 Elantra and 2016 Elantra GT vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of injury from metal fragments.
Generac and DR Power electric start pressure washers are recalled because the electronic start/stop button can malfunction and self-start the unit, creating a risk of serious injury or death from carbon monoxide poisoning in confined spaces. No injuries have been reported.