State
72,936 recalls have nationwide distribution and so reach Illinois. 11,603 additional recalls listed Illinois specifically in their distribution scope.
Of the 11,603 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 2,516 (22%) are Severe.
Which agencies issued them
These figures cover only the 11,603 recalls whose distribution notice names Illinois specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
17 Stories Furniture 14-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards. They violate the STURDY Act.
ProRider bicycle helmets are being recalled because they do not comply with the mandatory safety standard for impact attenuation, positional stability, labeling and certification.
Kluster Fun Tabletop Magnet Chess Games are being recalled because they contain loose high-powered magnets that fit within CPSC's small parts cylinder, posing an ingestion hazard to children.
LIVEHOM 11-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards. They violate the STURDY Act.
Aluminum Trailer Company is recalling certain 2023-2026 PL700 and PL750 recreational trailers because the generator exhaust is vented directly under the slide-out bedroom, letting carbon monoxide enter the cabin.
Abiomed is recalling the Impella RP, product code 0046-0011, because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Mojo Max Fusion XXX capsules are being recalled because FDA analysis revealed undeclared sildenafil at 13.1 mg per capsule and tadalafil at 13.8 mg per capsule. The FDA has classified this recall as Class I.
Abiomed is recalling the Impella RP Flex with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Abiomed is recalling the Impella RP with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
123Herbals is recalling Silintan 25-count pill bottles because FDA analysis revealed the presence of undeclared meloxicam. The FDA has classified this recall as Class I.
Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-210, because of the potential for rubber fragment detachment during use.
Mack Trucks is recalling 2022-2027 TerraPro trucks because engine software may allow starting while in gear, increasing crash risk.
ARBOC is recalling 2018-2026 Spirit of Freedom and Spirit of Mobility buses because incorrectly installed rear brake lines may cause the anti-lock brake system to malfunction.
Olympus is recalling ShockPulse-SE Lithotripsy System reusable probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
Volkswagen is recalling certain 2025–2026 Jetta vehicles because the transmission ground wire may not have been properly connected during assembly, creating an open electrical circuit that could increase fire risk.
Radnostix is recalling one batch of Sodium Iodide I-131 Therapeutic Oral Solution because of the presence of particulate matter caused by production issues.
Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-1218, because of the potential for rubber fragment detachment during use.
Mylan Pharmaceuticals is recalling two lots of Amnesteem (Isotretinoin) Capsules 40 mg after the product failed dissolution specifications.
Olympus is recalling ShockPulse-SE Lithotripsy System single use probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
Tippy Toes apple pear banana baby food (6 months & up) is being recalled due to potential contamination with patulin. Consumers who have purchased this product should not feed it to infants.
GE Healthcare is recalling Centricity Universal Viewer Zero Footprint Client because under certain workflows the patient information shown may not match the images displayed.
Teva Pharmaceuticals is recalling three lots of Metoprolol Succinate Extended-Release Tablets 200 mg after the product failed dissolution specifications.
Rising Pharma Holding is recalling one lot of Temozolomide Capsules 5 mg after an out-of-specification result was observed during nine-month long-term stability testing.
Roche is recalling cobas pro sample supply units on software versions before 03-02 because a defect can make the analyzer repeat the last calculated result for all later measurements.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 50 mg after the product failed dissolution specifications.