State
72,968 recalls have nationwide distribution and so reach Idaho. 3,517 additional recalls listed Idaho specifically in their distribution scope.
Of the 3,517 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,023 (29%) are Severe.
Which agencies issued them
These figures cover only the 3,517 recalls whose distribution notice names Idaho specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Altec is recalling 2024 FOSV-CA vehicles because an interconnect battery cable may overheat, increasing the risk of a fire.
Altec is recalling 2022-2025 ST600 vehicles with auxiliary engines because overloaded electrical circuits may overheat and increase the risk of fire.
Forest River is recalling 2025-2026 Entourage recreational vehicles because a suspension bolt may fail, causing the leaf spring to detach and increasing crash risk.
REV is recalling 2024-2026 Fleetwood Fortis and Holiday Rambler Invicta RVs with theater seats because theater seat fasteners may have damaged propane hoses, creating a fire hazard.
Autocar is recalling 2023-2026 Legend and Xpeditor vehicles because the steering wheel nut may be improperly secured, allowing the wheel to separate from the column.
About 2,400 Kogalla power banks are being recalled after two reports of lithium-ion batteries overheating and catching fire, causing one minor burn injury and about $3,300 in property damage.
About 630 Blossom children's two-piece loungewear sets are being recalled because they violate the mandatory flammability standard for children's sleepwear.
Hyundai is recalling 2024-2025 Santa Fe vehicles. The starter motor terminal cover may be improperly installed, causing electrical shorts that increase fire risk during crashes.
About 470 Almpal dissolved oxygen test kits are being recalled because the sulfuric acid bottle inside is not in child-resistant packaging, as the Poison Prevention Packaging Act requires.
About 610 Gunaito 10-drawer dressers sold on Walmart.com are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act stability standard.
About 98,350 Evermore Surprise Eggs are being recalled because the toy airplane inside contains lead above the federal lead content ban. No incidents have been reported.
GOODLES is recalling 61,176 cartons of Here Comes Truffle creamy truffle flavored cheddar and shells because the product contains cashews that are not declared on the label.
GOODLES Vegan Is Believin' Plant-Based White Cheddar with Spirals, 5.25 oz, is recalled for undeclared milk. The FDA classified the action as Class I. 129,660 cartons are affected.
Toyota is recalling certain 2025 Tacoma and Tacoma Hybrid vehicles because the front driveshaft CV joint may deform and break, impairing steering and risking vehicle rollaway while parked.
Abiomed is recalling specific Automated Impella Controllers with defective Pump Driver Circuit Assemblies that may cause decreased pump performance or pump stop. The defect triggers Impella Failure or Impella Stopped Controller Failure alarms.
Philips is recalling certain CT systems because the patient support table may descend unexpectedly to the lowest position due to a component misalignment during replacement.
Philips Allura Xper FD20 Biplane OR Table systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 5 units are affected.
Philips Brilliance iCT systems, model 728306, are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 210 units are affected.
Philips Allura Xper FD20 Biplane systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 268 units are affected.
Baxter is issuing an urgent recall for one lot of Continu-Flo Solution Sets, REF 2C8519, after customer reports of tubing separation. 14,400 units are affected.
Philips Brilliance CT 40 Channel, Brilliance CT 64 Channel and Ingenuity Flex systems are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 181 units are affected.
BeneVision N1 Patient Monitors are recalled because of the potential for activation of an abnormal alarm pause. 2,278 units are affected.
Vasoview Hemopro 3 Endoscopic Vessel Harvesting Systems are recalled after out-of-box failures including deformed jaw attachments, jaws not fully closed and lifted heater wire. 98 units are affected.
Philips Brilliance 16 Power, Brilliance CT 16 Slice and Brilliance CT 6 Slice systems are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 73 units are affected.
The Philips Allura Xper FD20/15 OR Table is recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. One unit is affected.