State
72,982 recalls have nationwide distribution and so reach Illinois. 11,606 additional recalls listed Illinois specifically in their distribution scope.
Of the 11,606 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 11,606 recalls whose distribution notice names Illinois specifically. The 72,982 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
LED gloves, model ST01, are being recalled because the coin battery compartment can be easily opened by children and the spare batteries are not in child-resistant packaging. About 9,900 units affected.
General Motors is recalling certain 2026 Cadillac VISTIQ and 2025 Cadillac LYRIQ vehicles because bolts attaching the high-voltage battery to the floor may be missing or loose, creating a fire risk in a crash.
The detachable cover of the Pura 4 Smart Home Fragrance Diffuser is being recalled because its magnets can detach. Three reports of magnets detaching have been received. About 851,400 units affected.
Aiho five-drawer dressers, model AP23-W, are being recalled because they are unstable if not anchored to the wall and fail the mandatory standard under the STURDY Act. About 1,900 units affected.
LIVACTI retractable mesh safety gates, model LT-BG01-3, are being recalled because a child's torso can fit through the opening between the gate and the floor. About 1,400 units are affected.
Creekwood Naturals Gum Spirits of Turpentine bottles are being recalled because they violate the mandatory standard for child-resistant packaging. About 9,000 units are affected.
Minecraft Light-Up Slap Ruler Bracelets are being recalled because the battery compartment can be opened easily by children, violating the mandatory toy standard. About 75,900 units affected.
Georgia Pine Gum Spirits of Turpentine in 4 oz glass bottles is being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act. About 20,000 units affected.
Tiffin is recalling certain 2023-2026 motorhomes with 2.0 litre engines because the secondary alternator controller programming was not properly updated, which can stall the engine.
Ferrari is recalling certain 2023-2025 Purosangue vehicles because the fuse box power supply and passenger-side footrest may contact each other, causing a short circuit that decreases braking ability.
Baxter SIGMA Spectrum Infusion Pump V6 units are being recalled because certain pumps may have an incorrect version of software. 14 units are affected.
Dubai emek Spread Pistachio Cacao Cream with Kadayif is being recalled after the FDA notified the firm that the product may be contaminated with Salmonella. 316 cases are affected.
Baxter SIGMA Spectrum Infusion Pump V8 units are being recalled because certain pumps may have an incorrect version of software. 28 units are affected.
BMW is recalling certain 2022-2025 i4, 2022-2024 iX, 2023-2024 i7 and 2024 i5 vehicles because electric drive motor software may shut down the high-voltage system, causing a loss of drive power.
Kilwin's Family Assortment in 9 oz, 14 oz, 28 oz and 42 oz sizes is being recalled because of undeclared pecans. 130 lbs in total are affected.
Kilwin's Truffle Assortments in 9.5 oz, 8 oz and 4.75 oz sizes are being recalled because of undeclared pecans. 130 lbs in total are affected.
Kilwin's Mocha Truffles, in 2.5 lb bulk and 4.75 oz retail units, are being recalled because of undeclared pecans. 130 lbs in total are affected.
The i-view video laryngoscope is being recalled because of the potential for faulty devices as a result of depleted batteries. 2,152 pieces are affected.
VITROS Chemistry Products CHE Slides supplied in Japan are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.
Crumbled Cookie Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.
Levothyroxine Sodium Tablets, USP 50 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 54,227 bottles affected.
The NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 516 US units affected.
Levothyroxine Sodium Tablets, USP 175 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 2,344 bottles affected.
VITROS Chemistry Products Performance Verifier II is being recalled because quality control drift can occur with certain cholinesterase slide lots, which could produce erroneous patient results.
Chocolate Crunch Cake Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.