State
73,566 recalls have nationwide distribution and so reach Illinois. 11,652 additional recalls listed Illinois specifically in their distribution scope.
Of the 11,652 recalls naming Illinois we have scored against our rubric, 2,050 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,018 (26%) are Severe.
Which agencies issued them
These figures cover only the 11,652 recalls whose distribution notice names Illinois specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Forest River is recalling 2022 East to West Alta and Palomino SolAire travel trailers because incomplete welds on the swing-up table base may cause it to drop unexpectedly, increasing injury risk.
Daimler Trucks North America is recalling 2023 Freightliner Business Class M2 trucks due to a u-joint pinch bolt that may detach from the steering shaft, causing loss of steering control and increasing crash risk.
Goodyear is recalling specific G159 tires because the tread may separate, increasing the risk of a crash. Owners should contact dealers for free replacement.
Backcountry Access Tracker4 Avalanche Transceivers are being recalled because the toggle switch can separate from the unit and prevent it from switching to search mode, which could prevent rescuers from locating a buried skier.
Asweets is recalling about 13,300 Wonder & Wise baby activity walkers because rubber rings on the rear wheels can detach, posing a strangulation hazard to young children. No injuries have been reported.
Communicorp is recalling about 600,000 six-inch Aflac plush promotional ducks distributed to Aflac employees and customers from February 2009 through March 2021. The ducks contain phthalates and lead levels that exceed federal standards and pose a risk if ingested by young children.
Joey Clothing is recalling about 15,930 children's robes sold online because they fail to meet flammability standards for children's sleepwear, posing a risk of burn injuries.
Winnebago is recalling 2020 ERA motorhomes because damaged burner control valves may cause a gas leak, increasing the risk of fire.
Demdaco microwavable bowl holders can char and catch fire when microwaved for the recommended time. The company received three reports of charring incidents and is offering refunds.
Electrolux is recalling about 367,500 Frigidaire and Electrolux refrigerators because the ice level detector arm in the ice maker can break apart and fall into the ice bucket, creating a choking hazard.
Target is recalling about 120,000 children's pajama sets because they fail to meet federal flammability standards for sleepwear, posing a burn injury risk to children. Consumers should return the pajamas to Target for a full refund.
General Motors is recalling certain 2022 Cadillac XT6 vehicles because the brake fluid reservoir cap may be missing its required warning label. Without the label, brake fluid could become contaminated with debris, affecting brake performance.
The FDA is recalling approximately 4,449 Sara Plus Active Floor Lift devices due to a fire hazard. The devices may emit smoke or ignite, posing a risk to users and staff.
Olympia Compounding Pharmacy recalls a multi-drug injectable compound (lot B41C22-22) due to inability to assure sterility. The recall affects 1,159 vials distributed nationwide.
Olympia Compounding Pharmacy recalls 911 vials of Ondansetron Hydrochloride (1 mg/mL) due to lack of sterility assurance. The product was distributed nationwide in the USA, Puerto Rico, and US Virgin Islands.
Dalton Enterprises is recalling 2021-2022 Adam J2040 horse trailers because damaged burner control valves may cause a gas leak, increasing fire risk.
Olympia Compounding Pharmacy is recalling 9,102 vials of Phenylephrine 1 mg/mL due to lack of assurance of sterility. The affected vials were distributed nationwide in the United States, Puerto Rico, and US Virgin Islands.
Olympia Compounding Pharmacy is recalling Lipostat-Plus vials nationwide due to lack of sterility assurance. Approximately 4,843 vials were distributed across the USA, Puerto Rico, and US Virgin Islands.
Olympia Compounding Pharmacy recalls 2,333 vials of Sodium Selenite 200 mg/mL injection due to a lack of assurance of sterility. The product was distributed nationwide in the USA, Puerto Rico, and the U.S. Virgin Islands.
Olympia Compounding Pharmacy recalled 1,710 vials of RE-2 injectable medication due to lack of assurance of sterility. Affected vials were distributed nationwide in the USA, Puerto Rico, and the US Virgin Islands.
Olympia Compounding Pharmacy is recalling 1,597 vials of Magnesium Chloride injection due to lack of sterility assurance. The product was distributed nationwide in the USA, Puerto Rico, and the US Virgin Islands.
Olympia Compounding Pharmacy is recalling SB-5, a multi-dose injectable medication, due to lack of assurance of sterility. The product was distributed nationwide; patients should contact their healthcare provider immediately.
Olympia Compounding Pharmacy is recalling Lidocaine 1%/Epinephrine 1:100,000 injection vials due to lack of sterility assurance. The recall affects 310 vials distributed nationwide.
Olympia Compounding Pharmacy is recalling Formula F1, a compounded injectable medication, due to lack of sterility assurance. The 1,703 vials were distributed nationwide.
Olympia Compounding Pharmacy recalls 6,113 vials of Olympia Mineral Blend injectable due to lack of assurance of sterility. The product was distributed nationwide; patients should not use it and should consult their healthcare provider.