State
72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Change Healthcare is recalling Cardiology Hemo Software (version 14.3.2 and 15.0.1) because a software update may cause the system to unexpectedly shut down. The recall affects 29 systems distributed across multiple US states and international locations.
The Harvard Drug Group LLC is recalling 23,232 cartons of Gabapentin Capsules 100 mg (Lot# M05205, Exp Date 10/2026) distributed nationwide due to inadequately sealed blister packaging that may compromise product integrity.
Philips Ultrasound, Inc. is recalling Philips XL14-3 Transducers because they were refurbished beyond their useful life, which may affect device performance and patient safety during ultrasound examinations.
Philips Ultrasound, Inc. is recalling 5,230 Philips L12-4 ultrasound transducer devices that were refurbished beyond their useful life. Affected units were distributed domestically and to numerous countries worldwide.
Gabapentin Capsules 100 mg from Major Pharmaceuticals are being recalled because of a defective container: the blister packaging was inadequately sealed. 3,527 bags are affected.
ADVIA 120/2120/2120i SETpoint Calibrator lots are being recalled because they have the incorrect platelet value assignments for ADVIA hematology systems. 2,020 units are affected.
C.R. Bard Inc is recalling certain BD Heyman Follower Coude Tip catheters because the packaging may display the incorrect French size, which could lead to use of the wrong size device.
Philips C5-1 Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Philips Ultrasound is recalling 5,230 L8-4 transducer units that were refurbished beyond their useful life, which may affect device safety and performance. The units were distributed nationwide and internationally.
Philips Ultrasound is recalling Philips eL18-4 Transducers because they were refurbished beyond their useful life, which may affect device performance and patient safety.
Philips X7-2t Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Philips Ultrasound, Inc. is recalling Philips C5-2 Transducers because they were refurbished beyond their useful life. The affected devices were distributed domestically nationwide and internationally across 49 countries.
Philips S7-3t Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Eight Valeda Light Delivery Systems are being recalled because US customers were shipped devices configured for the European Union that could not be plugged into the outlet.
AvKARE is recalling Pitavastatin 2 mg tablets nationwide due to failed impurity and degradation specifications. The affected lots do not meet quality standards for chemical purity.
Motiv Power Systems is recalling 2021-2024 F-59 BEV chassis vehicles because improperly sealed high-voltage battery packs may allow liquid entry, increasing the risk of fire or shock.
Motor Coach Industries is recalling specific 2025-2026 bus models because emergency exit labels may be placed in the wrong location, potentially delaying exit use.
NHTSA is recalling 2025 Bontrager and Skinny Guy campers because carbon monoxide detectors may be missing, increasing the risk of injury to occupants.
Ford is recalling certain 1.5L EcoBoost cylinder heads and long block engines sold as replacement parts because improper manufacturing may cause oil leaks, increasing the risk of fire or loss of drive power.
Reading Truck Group is recalling 2021 Rail Gear HD trucks because welds may crack, causing the front rail gear to shift and drag on the road, increasing crash risk.
Jaguar Land Rover is recalling 2020–2025 Range Rover Evoque vehicles because the passenger air bag may tear during deployment, reducing occupant protection and risking burn injury from escaping gases.
Polestar is recalling certain 2025 Polestar 3 vehicles because water may damage electrical connectors between the engine bay and front bumper, which can cause loss of power steering assist and increase crash risk.
Shyft Group is recalling 2015-2025 Utilimaster Truck Body vehicles because a signal converter failure can cause brake lights and turn signals to stop working.
Ford is recalling certain 2021–2023 Ford and Lincoln vehicles because the low-pressure fuel pump may fail, causing engine stalls while driving and increasing crash risk.
Kawasaki is recalling certain 2024–2025 Ninja ZX-6R motorcycles because the engine may lose power during operation due to crankshaft bushing seizure, increasing crash risk.