State
72,940 recalls have nationwide distribution and so reach Nevada. 5,692 additional recalls listed Nevada specifically in their distribution scope.
Of the 5,692 recalls naming Nevada we have scored against our rubric, 951 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,476 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,692 recalls whose distribution notice names Nevada specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Get Tested International AB is recalling 71 units of its Allergy Test IgE because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its Gut Microbiome Test Medium because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its GI Microbiome Profile XL because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1361 units of its Herpes (HSV-1 & HSV-2) Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 50 units of its Heavy Metals Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 18 units of its Neurotransmitters Plus because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its Food Allergy Panel Test (IgE) because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 940 units of its Lyme Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 36 units of its NAD Profile Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 19 units of its Hair Mineral Analysis because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 35 units of its Fecal Occult Blood Test because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 13536 containers of Nivagen Zinc Oxide Ointment over current good manufacturing practice deviations.
Get Tested International AB is recalling 2 units of its Pregnancy Test because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 9600 containers of Lanashield Skin Barrier over current good manufacturing practice deviations.
Get Tested International AB is recalling 31 units of its Leaky Gut Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 239 units of its H pylori (Peptic ulcer) Test because the product was distributed without premarket approval or clearance.
Philips North America is recalling 6 CT 5300 systems because a tube heat exchanger whose screws are not tightened after replacement may detach and damage other components.
Aizu Olympus is issuing a recall covering 6,578 OER-Mini units to inform customers about pertinent warnings and cautions, recommended maintenance schedules and repair training requirements.
Aizu Olympus is issuing a recall covering 6,578 OER-Elite units to inform customers about pertinent warnings and cautions, recommended maintenance schedules and repair training requirements.
Aizu Olympus is issuing a recall covering 6,578 OER-Pro units to inform customers about pertinent warnings and cautions, recommended maintenance schedules and repair training requirements.
Chrysler is recalling specific MOPAR Brake Pedal Assemblies because the pedal may collapse, causing a loss of brake function and increasing crash risk.
Chrysler is recalling 2024 Dodge Hornet and Alfa Romeo Tonale PHEV vehicles because the brake pedal may collapse, causing a loss of brake function and increasing crash risk.
Chrysler is recalling 2024 Alfa Romeo Giulia vehicles because a misrouted wiring harness may cause headlights to fail, increasing crash risk.
Jayco is recalling specific 2025-2026 recreational vehicles because incorrect weight ratings on labels may lead to unintentional overloading and increased crash risk.
Daimler Trucks North America is recalling specific Thomas Built Buses because wheelchair restraints may fail to lock, increasing injury risk.