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.
Medtronic is recalling one lot of the Octopus Nuvo Tissue Stabilizer after identifying an assembly issue in which the short and long tubes were attached to the wrong ends of the canister.
Vizcure Pharmaa Private Limited is recalling Vista Hypromelose Dry Eye Relief eye drops due to lack of assurance of sterility. The products were not manufactured in conformance with current good manufacturing practices.
LEO Pharma is recalling its ADBRY injection drug due to particulate matter (wool fiber) found in one unit, which may affect sterility. The recall covers 11,407 units distributed nationwide.
Medline Industries, LP is recalling Medline Sterile Saline Wound Wash because the product may not meet required sterility assurance levels.
Olympus is recalling 899 units of its 8 mm Resection Sheath (Model A42011A) used in gynecological procedures after receiving complaints that the ceramic tip can break during use.
Wizcure Pharmaa is recalling all lots of Vista Meibo Tears Propylene Glycol 0.6% eye drops because the products were not manufactured in conformance with current good manufacturing practices.
Wizcure Pharmaa is recalling all lots of BioGlo Fluorescein Sodium Ophthalmic Strips in 100-strip packs because the products were not manufactured in conformance with current good manufacturing practices.
Olympus is recalling its Resection Sheath model A2666T, used for endoscopic diagnosis and treatment in urological applications, after complaints that the ceramic tip of the sheath can break.
Wizcure Pharmaa is recalling all lots of Bio Glo Fluorescein Sodium Ophthalmic Strips in 300-strip packs because the products were not manufactured in conformance with current good manufacturing practices.
Olympus is recalling its Sheath, 10 Fr, model A37004A, used for endoscopic diagnosis and treatment in urological applications, after complaints that the ceramic tip can break.
Olympus is recalling its Inner Sheath Model A2642, a medical device used in urological procedures, after receiving complaints that the ceramic tip can break during use.
Agiliti Health - Ellis is recalling Adapt Pumps (Model 61600200) because the Microclimate Management function may fail to re-engage after using the Autofirm function.
Valley Springs Artesian Gold, LLC is recalling various sizes of Valley Springs 100% Natural Bottled Water because the product was bottled under insanitary conditions.
Edermy LLC is recalling PIE PAK models P2HC-A, P2HC-S and P2HC because the devices lack 510(k) clearance from the FDA.
Valley Springs Artesian Gold, LLC is recalling Valley Springs Steamed Distilled Water because it was bottled under insanitary conditions.
Edermy LLC is recalling the PIE Trolley System, model 2005, because the device lacks 510(k) clearance from the FDA.
Valley Springs Artesian Gold, LLC is recalling 7,840 units of its 1-gallon bottled water due to water being bottled under insanitary conditions. No illnesses have been reported.
Slate Run Pharmaceuticals is recalling Eptifibatide Injection due to a labeling error on the carton, which incorrectly describes the dosing instructions.
Ajinomoto Foods North America is expanding a recall for frozen fried rice, ramen, and shu mai products due to possible glass contamination. No injuries have been reported.
Ford Motor Company is recalling certain 2025 and 2026 F-250 SD and F-350 SD vehicles due to a potential driveshaft failure that could lead to a loss of power.
Ford Motor Company is recalling certain 2026-2027 E-350 and E-450 vehicles because the backup alarm may fail to sound, increasing the risk of a crash.
Ford Motor Company is recalling certain 2025-2026 Explorer vehicles because the headlight system software may cause the passenger-side headlight to turn in the wrong direction during curves.
Ford is recalling certain 2021-2026 Bronco and 2021-2024 Edge vehicles because the rearview camera may fail to display an image due to an overheating module.
Ford is recalling 2026 Lincoln Navigator vehicles because the driver seat software may malfunction at low speeds, causing the seat to move unexpectedly and increasing crash risk.
Ford is recalling certain 2025 vehicles due to a potential EGR valve failure that could cause an unexpected loss of drive power, increasing crash risk.