State
72,940 recalls have nationwide distribution and so reach Delaware. 3,435 additional recalls listed Delaware specifically in their distribution scope.
Of the 3,435 recalls naming Delaware we have scored against our rubric, 477 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 937 (27%) are Severe.
Which agencies issued them
These figures cover only the 3,435 recalls whose distribution notice names Delaware 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 1557 units of its Vitamin D-Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 4 units of its Organic acids Test because the product was distributed without premarket approval or clearance.
Blossom Pharmaceuticals is recalling 2,592 bottles of WeCare Zinc Oxide Ointment, 15 oz, over current good manufacturing practice deviations.
Get Tested International AB is recalling 258 units of its HPV Antigen Test 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 5187 units of its Iron Deficiency Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 8 units of its Fructose Intolerance Test because the product was distributed without premarket approval or clearance.
Philips Ultrasound is recalling 4,819 Lumify Diagnostic Ultrasound Systems because compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imaging.
Get Tested International AB is recalling 1 unit of its Drug Test Small (4 substances) because the product was distributed without premarket approval or clearance.
Teva Pharmaceuticals USA is recalling 15,944 cartons of Testosterone Gel 1% unit-dose packets because a defect in the side-seal allows leakage of product.
Get Tested International AB is recalling 45 units of its Intestinal Worms Test because the product was distributed without premarket approval or clearance.
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.
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-Mini 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.
Daimler Trucks North America is recalling 2026-2027 Thomas Built Buses Saf-T-Liner C2 models because the wheelchair restraint retractor may fail to lock, increasing injury risk.
Jayco is recalling specific 2025-2026 recreational vehicles because incorrect weight ratings on labels may lead to unintentional overloading and increased crash risk.
Great Dane is recalling 2024-2025 Champion trailers because insufficient lubrication on the liftgate cylinder pin can cause it to seize, leading to liftgate failure and injury risk.
Daimler Trucks North America is recalling specific Thomas Built Buses because wheelchair restraints may fail to lock, increasing injury risk.
Keystone is recalling 2026 Impact and Carbon trailers because patio rail kits may be missing parts, preventing panels from being properly attached.
Chrysler is recalling 2024 Alfa Romeo Giulia vehicles because a misrouted wiring harness may cause headlights to fail, increasing crash risk.
ARBOC is recalling 2025 Spirit of Freedom transit buses because wheelchair retractors may fail to lock, increasing injury risk during transit.
ARBOC Specialty Vehicles is recalling 2025 Spirit of Freedom and Spirit of Mobility buses because wheelchair retractors may fail to lock, increasing injury risk.
Micro Bird is recalling 2026 G5 transit buses because a loose power cable connection may cause the air conditioning control board to overheat and melt, increasing the risk of a fire.