State
72,968 recalls have nationwide distribution and so reach New Mexico. 3,625 additional recalls listed New Mexico specifically in their distribution scope.
Of the 3,625 recalls naming New Mexico we have scored against our rubric, 747 (21%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 647 (18%) are Severe.
Which agencies issued them
These figures cover only the 3,625 recalls whose distribution notice names New Mexico specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 47,000 Matrix and Vision treadmills are being recalled because the power cord can become loose from the power socket, posing a fire hazard.
About 35,300 Magellan Odyssey Rocker Chairs sold by Academy Sports + Outdoors are being recalled because the chairs' legs can break.
About 340 Gagaku ice cream shop toy playsets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.
About 7,500 Topkay Torch Lighters are being recalled because they do not have the child-resistant mechanisms required by the mandatory standard for multipurpose lighters.
About 4,520 Cumbor retractable safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor.
Blue Bird is recalling 2026-2027 Vision and All American school buses because side and rear windows may have illegible DOT markings, failing federal safety standards.
Blue Bird is recalling one 2026 Vision transit bus because side or rear windows may have illegible DOT markings, failing federal safety standards.
Herbs Forever is recalling 45 units of HerbsForever Hingwastika Churna Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The action is Class I.
Herbs Forever is recalling 45 units of HerbsForever Gastro Care Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The FDA has classified the action as Class I.
One Roof LLC is recalling 197 Atwater's Holiday Cookie Tins over undeclared tree nut allergens: almonds, pecans and walnuts.
Volkswagen is recalling certain 2023-2024 ID.4 vehicles because the high voltage battery cell modules may contain misaligned electrodes that can result in a battery fire.
Ford is recalling 2026 Explorer vehicles because the windshield may not be properly bonded, posing an injury risk in a crash.
Oshkosh is recalling 230 2025 NGDV and NGDV Electric vehicles because rear axle hub fasteners may loosen, potentially causing the wheel to detach.
Gold Star Distribution is recalling Claritin over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
ICU Medical is recalling 64,290 Portex Spinal Trays because syringes may have a crack on the collar, which may lead to delayed or repeated blood draws and blood leakage.
Gold Star Distribution is recalling Liquid NyQuil over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Philips Medical Systems Nederland is recalling 990 Azurion R3.0 systems over nine identified software issues, including loss of X-ray after a pedal tap and continuous restart.
Gold Star Distribution is recalling Benadryl over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling Personal Care Ice Gel over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Eureka Inc is recalling 32 cases of ground cinnamon in 100g clear plastic containers over elevated levels of lead.
Gusto Group is recalling 7 cases of Klong Kone shrimp paste after the product tested high for lead.
Gold Star Distribution is recalling Petroleum jelly over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling Tylenol over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
GE Medical Systems Israel is recalling 38 MAXXUS systems because units past end of guaranteed service may have been moved without adequate detector support, risking a detector fall.
Thoratec is recalling 8,399 CentriMag blood pump products after reports that the pump may not fit or lock securely into the motor using the screw-in locking feature.