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.
Honda is recalling certain CMX300, CMX500, and SCL500 motorcycles because the handlebar lock screw may loosen and detach, potentially interfering with steering.
General Motors is recalling certain 2026 Cadillac Escalade, GMC Sierra EV, and Chevrolet Silverado EV models because an improperly secured battery component may increase the risk of a fire.
About 178,000 OCTROT electric throws and blankets can have their cord detach and ignite. The firm reports 555 incidents resulting in 27 fires and 15 burn or electrical shock injuries.
About 1,034 Mommy's Baby Lovely Deluxe Baby Doll Playsets sold on Temu contain small parts that pose a choking hazard to children under three. No injuries reported.
BenQ GV31 portable projectors can overheat because of their lithium-ion battery. The firm has received three overheating reports, one of which caused burns to a consumer's hands.
About 1,980 KAIFAM 5-drawer metal dressers sold on Amazon are unstable when not anchored to a wall and violate the STURDY Act standard. No injuries reported.
About 12,800 EnHomee 15-drawer dressers sold on Amazon are unstable when not anchored to a wall and violate the STURDY Act standard. No injuries reported.
About 55,350 Fantastic Four drinking cups and Captain America popcorn helmets with LED lights have accessible button cell batteries and lack the warning labels required by Reese's Law.
An additional 195 Cpzzkq baby loungers are recalled because the padding can obstruct an infant's breathing, breaching the mandatory infant support cushion standard. No injuries reported.
Autocar is recalling 2023-2027 ACTT terminal tractors because the ABS Electronic Control Unit may be improperly secured, potentially causing system failure and increasing crash risk.
Joyin expanded its recall of Sloosh dive sticks to models 40003 and 16154 alongside model 40041. The sticks exceed the federal compression limit and pose an impalement hazard. No injuries reported.
105 Mangohood Direct children's tower stools, model LT003, can collapse or tip over, and a child's torso can fit through openings on the front and back. No injuries reported.
About 91,000 Woodure toddler tower stools can collapse or tip over, with openings a child's torso can pass through. Woodure reports 22 incidents and 15 injuries involving scrapes, cuts and bruises.
Jake's Fireworks recalled about 132,440 World Class Fireworks "Skull Strobe" rockets because they can explode before reaching their intended height. No injuries have been reported.
Brinkley RV is recalling 2027 Model I trailers because the exterior ladder may not be properly secured, posing a risk of injury if it detaches.
HARPPA recalled 47,166 Nordi foldable toddler tower stools that can collapse or tip over, with openings a child's torso can pass through. Three incidents and two minor injuries reported.
Medline Industries, LP is recalling specific C-Section convenience kits because they contain Bupivacaine Hydrochloride in Dextrose Injection, USP, which is subject to a voluntary recall due to quality issues.
JB Chemicals and Pharmaceuticals Ltd is recalling 34,020 bottles of Cetirizine Hydrochloride Tablets USP 5 mg because some tablets were found to contain Ranitidine due to cross contamination.
Medline Industries, LP is recalling certain MEDLINE medical procedure convenience kits because they contain ICU Medical, Inc. pain management kits that may be ineffective.
Modern Warrior Life, LLC is recalling Modern Warrior Ready dietary supplements because they contain unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium 125 mcg tablets (Lot N02266, Exp. 11/2026) nationwide due to subpotency, meaning the tablets may contain less active ingredient than labeled.
Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 25 mcg, due to subpotency. The recall affects nationwide U.S. distribution of specific lot numbers.
Total Nutrition Inc is recalling TNVitamins 100% Organic Moringa Capsules and Powder due to Salmonella contamination. The recall affects 8,492 units distributed nationwide.
Rohto Digi-Eye cooling eye drops are recalled due to a lack of assurance of sterility. The recall affects 65,219 cartons distributed nationwide in the U.S.
The FDA is recalling 278 Power F2 Powered Fastening Systems made by Ferno-Washington Inc due to potential roller wear and rail deformation that could prevent stretcher movement.