State
73,187 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 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Dropcases Limited is recalling Lectron Vortex adapters that may not latch securely to chargers, increasing the risk of electrical shock.
Chrysler is recalling certain 2021 Ram ProMaster vehicles because an insecure ground connection may render the electronic stability control inoperative, failing FMVSS 126.
Crosman is recalling about 2,500 Icon Air Rifles because an uncocked and loaded rifle can discharge unexpectedly if jolted or dropped, posing an injury hazard. One unintended discharge has been reported, though no injuries have occurred.
Chrysler is recalling certain 2023 Jeep Grand Cherokee and Grand Cherokee L vehicles because improperly fastened screen module connections may prevent the rearview camera image from displaying.
Chrysler is recalling certain 2022-2024 Jeep Grand Cherokee and Grand Cherokee L vehicles because an improperly connected coaxial cable may prevent the rearview camera image from displaying.
Chau River Sports Outdoors is recalling about 200 kids' bike helmets sold on Temu.com because they fail to meet federal safety requirements and may not protect children's heads in a crash.
3M is recalling about 40,000 Peltor X4 Series earmuffs sold from May through June 2023 because cracks can develop in the plastic cups, allowing overexposure to loud noise. No injuries have been reported.
Crate & Barrel is recalling about 3,200 Hampshire Cribs sold online from June 2022 through November 2023 because mattress support pins can become loose, posing a fall hazard. No injuries have been reported.
Philips is recalling the Trilogy Evo Universal Ventilator for a software defect that triggers false low-battery or power-loss alarms despite sufficient power, risking sudden ventilation loss.
Draeger Medical is recalling approximately 16,841 Dräger Perseus A500 Anesthesia Workstations due to unexpected shutdown while operating on battery power. The devices have been distributed nationwide and internationally.
Philips Respironics is recalling 789 Trilogy Evo O2 ventilators due to a software defect that can trigger a false power alarm despite sufficient power, potentially causing sudden loss of ventilation in pediatric and adult patients.
Outset Medical is recalling Tablo Hemodialysis Systems because their silicone tubing may contain unremoved polychlorinated biphenyl acids (PCBAs), which could cause skin conditions, liver damage, reproductive harm, or cancer.
Philips Respironics is recalling the LifeVentEVO2 ventilator due to a software malfunction that can trigger a false Battery Depleted or Loss of Power alarm when power is sufficient, potentially causing sudden loss of ventilation.
Philips Respironics recalls 1,233 Garbin EVO ventilators. A software defect in the battery and power alarm system may cause sudden loss of ventilation despite adequate power supply.
SonarMed Inc is recalling the AW-S035 NEO airway monitoring sensor due to failure to detect partial obstructions. The defect may prevent the device from alerting clinicians to airway obstruction.
BMW is recalling 2014-2015 2, 3, and 4 Series vehicles because head air bag inflators may fail, posing an injury risk.
AvKARE recalls Atovaquone Oral Suspension due to potential Bacillus cereus contamination of a non-sterile product. The recalled lot (AW0221A, Exp. 08/30/2025) was distributed nationwide; 153 cartons affected.
Philips is recalling 56,012 Trilogy EV300 ventilators due to a software defect that can trigger a false Battery Depleted or Loss of Power alarm despite adequate power, risking sudden loss of ventilation.
Amneal Pharmaceuticals is recalling Vancomycin Hydrochloride Oral Solution nationwide due to manufacturing overfilling causing superpotency with higher-than-labeled concentration. The FDA classified this as Class I.
SonarMed Inc is recalling 690 units of the AW-S030 NEO SONARMED SENSOR because the sensor fails to detect partial airway obstruction. The devices were distributed across 20 US states.
SonarMed Inc is recalling the AW-S025 NEO SONARMED SENSOR 2.5MM airway monitoring device due to a malfunction that causes it to fail detecting partial obstruction, potentially preventing clinicians from identifying compromised airways.
Philips Respironics is recalling the Trilogy Evo ventilator (76,713 units) because it may suddenly stop ventilating when a false Battery Depleted or Loss of Power alarm triggers despite sufficient power available.
Philips Respironics is recalling Aeris EVO ventilators due to a software defect that may cause false battery or power alarms while the device retains adequate power, risking sudden loss of ventilation in pediatric and adult patients. Approximately 775 units are affected.
Philips is recalling certain Intera 1.5T MRI systems because the patient support table floor plate may be incorrectly installed, which could affect patient safety.
Randox Laboratories is recalling its Microalbumin Calibrator Series due to a negative bias in its calibration. This could misclassify patient results and affect Quality Control procedures by up to 12%.