State
72,820 recalls have nationwide distribution and so reach Illinois. 11,601 additional recalls listed Illinois specifically in their distribution scope.
Of the 11,601 recalls naming Illinois we have scored against our rubric, 2,039 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,514 (22%) are Severe.
Which agencies issued them
These figures cover only the 11,601 recalls whose distribution notice names Illinois specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Fitueyes, Inc. is recalling Laziza Dressers because they pose tip-over and entrapment hazards that could cause serious injury or death to children.
Volvo Trucks is recalling 2026-2027 VNL and VNR models because center roof marker lights may fail to illuminate, reducing visibility.
KC Imports and Exports is recalling Laser & LED Light Mini Laser Pointer Keychains because button cell batteries can be easily accessed by children, posing a risk of serious injury or death.
OKK Trading, Inc. is recalling three models of Easter LED Headbands because the lithium coin batteries can be easily accessed by children, posing a risk of serious injury or death.
Chrysler is recalling specific Mopar seat belt assemblies because the rear outboard belts may twist and fail to retract, increasing injury risk.
Toyota is recalling 2026 bZ Woodland vehicles equipped with a tow converter due to an electrical short circuit risk that can disable stability control and keep brake lights on.
Chrysler (FCA US, LLC) is recalling certain 2023-2026 Alfa Romeo Tonale and 2023-2025 Dodge Hornet vehicles because the rear outboard seat belts may fail to retract properly.
Syera is recalling Space Astronaut LED Finger Lights sold on Temu because the button cell batteries can be easily accessed by children, posing a risk of serious injury or death if swallowed.
Evenflo is recalling Revolve180 Litemax NXT child seats manufactured through March 31, 2025, because a miscalibrated level indicator may cause the seat to sit too upright, increasing injury risk in a crash.
Toyota is recalling certain 2024 Tacoma hybrid and 2024-2025 Tacoma vehicles because their rear shock absorber assemblies may corrode and fail, potentially detaching the external oil reservoir and creating a road hazard.
International is recalling 2027 HV, HX, LT, MV, and RH trucks because a wiper nut may loosen, causing wipers to disconnect and reducing visibility.
Mack Trucks is recalling 2027 Anthem and Pioneer models because center roof marker lights may fail to illuminate, reducing visibility.
ResMed is recalling Astral 100/150 ventilators because supercapacitor electrolyte leakage can damage the charger chip, trigger a fail-safe state, and interrupt ventilation therapy.
Windstone Medical Packaging is recalling 15 AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues reported by Elevaris Medical Devices Inc.
Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula (Model 77522) due to potential pinhole leaks in the wire-wound body during use.
Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula Model 77722 due to potential pinhole leaks in the wire-wound body during use.
Mylan Pharmaceuticals is recalling one lot of Mycophenolate Mofetil for Injection, 500 mg/vial, because precipitate was found in the vials. The recall covers 5,688 vials distributed nationwide.
Permobil is recalling M3 Corpus Power Wheelchairs with firmware version 1.26.2 because the firmware lacks a speed restriction when the seat lift exceeds 50 mm, which may cause falls or tip-overs.
Medicom is recalling specific lots of Ritmed Neurological Sponges (Models 55992C to 55998C) because of potential unexpected variability in endotoxin levels.
Medtronic recalls 21,290 EOPA arterial cannulas (BLUNT 22FR) because pinhole leaks may occur during bypass, risking hypovolemia, vessel injury, hypotension, ischemia, and organ dysfunction.
Instrumentation Laboratory is recalling Bar Code Reader (BCR) wands used with GEM Premier 5000 and 7000 systems because they may assign patient results to the wrong patient ID.
Medtronic is recalling its EOPA arterial cannula because pinhole leaks may occur during bypass, risking hypovolemia, vessel injury, and organ dysfunction.
Instrumentation Laboratory is recalling the GEM Premier 5000 portable blood analyzer system because bar code reader wands may assign patient results to the wrong patient ID. The recall affects 21 units distributed nationwide.
Stryker GmbH is recalling Hoffmann II Carbon Connecting Rods (catalog 50796060) because they may crack after cleaning and sterilization. The recall covers all lots and about 9,658 units distributed worldwide.
Windstone Medical Packaging, Inc. is recalling specific lots of AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits because of potential unexpected variability in endotoxin levels.