State

Illinois product recalls

73,570 recalls have nationwide distribution and so reach Illinois. 11,652 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total: 11,652
Critical: 2,050
Severe: 3,018
Most recent: 2026-10-24

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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24451–24475 of 85222

SevereFDA (Devices)·Z-0694-2022·2022-03-16
Medtronic TurboHawk Plus Directional Atherectomy System Recalled Due to Design Defect
ev3 Inc. is recalling the Medtronic TurboHawk Plus Directional Atherectomy System due to design similarities to a device with reported tip detachment and embolization incidents. The FDA has classified this as a Class I recall.
Product
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Multi-vessel, Catalog number THP-M. For use in peripheral vasculature.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0695-2022·2022-03-16
Medtronic TurboHawk Plus atherectomy system recalled for potential tip detachment
The Medtronic TurboHawk Plus Directional Atherectomy System (catalog THP-S) is being recalled due to design similarities to another device that experienced tip detachment and embolization. The recall affects 245 devices distributed nationwide.
Product
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Small Vessel, Catalog number THP-S. For use in peripheral vasculature.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0850-2022·2022-03-16
Strawberry Coffee Cake Recalled for Undeclared Egg, Milk, and Wheat Allergens
Chicago Sweet Connections is recalling its Strawberry Flavor Coffee Cake due to undeclared allergens: egg, milk, and wheat. Consumers with allergies to these ingredients should not consume the product.
Product
Chicago Sweet Connections: Coffee Cake - Strawberry Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
Category
Food
Distribution
2 states
HighFDA (Food)·F-0844-2022·2022-03-16
Chicago Sweet Connections Coffee Cake Recalled for Undeclared Allergens
Chicago Sweet Connections is recalling its Coffee Cake - Cheese Flavor due to undeclared allergens: egg, milk, and wheat. The product was distributed to retail locations in Illinois and Wisconsin.
Product
Chicago Sweet Connections: Coffee Cake - Cheese Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
Category
Food
Distribution
2 states
HighFDA (Food)·F-0849-2022·2022-03-16
Chicago Sweet Connections Coffee Cake Contains Undeclared Egg, Milk, and Wheat Allergens
Chicago Sweet Connections is recalling its Coffee Cake - Raspberry Flavor because it contains undeclared egg, milk, and wheat allergens that are not listed on the product label.
Product
Chicago Sweet Connections: Coffee Cake - Raspberry Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
Category
Food
Distribution
2 states
HighFDA (Food)·F-0851-2022·2022-03-16
Del Monte Bubble Fruit cups recalled for potential metal fragments
DEL MONTE FOODS INC is recalling Del Monte Bubble Fruit Tropical Mixed Fruit Cup Snacks due to potential metal fragments approximately 2–3 mm in size. No injuries have been reported.
Product
Del Monte Bubble Fruit - Tropical Mixed Fruit Cup Snacks. Mixed fruit and popping boba with sweetened juice. 3.5 0z (4 pack), 6 x 4 pack sleeves per carton UPC: 24000 25236
Category
Food
Distribution
29 states
HighFDA (Food)·F-0847-2022·2022-03-16
Coffee Cake with Undeclared Egg, Milk, and Wheat Allergens
Chicago Sweet Connections is recalling Coffee Cake - Custard Flavor due to undeclared allergens: egg, milk, and wheat. Consumers with allergies to these ingredients should not consume the product.
Product
Chicago Sweet Connections: Coffee Cake - Custard Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
Category
Food
Distribution
2 states
HighFDA (Food)·F-0829-2022·2022-03-16
Factor 75 Chili Meal Recalled for Undeclared Milk Allergen
Factor 75 Fiery Beef & Black Bean Chili meals are being recalled due to undeclared milk allergen. The product was distributed nationwide and may affect consumers with milk allergies.
Product
Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer
Category
Food
Distribution
49 states
HighFDA (Food)·F-0843-2022·2022-03-16
Chicago Sweet Connections Coffee Cake Recalled for Undeclared Egg, Milk, and Wheat Allergens
Chicago Sweet Connections coffee cake may contain undeclared egg, milk, and wheat allergens. The product was distributed to retail locations in Illinois and Wisconsin.
Product
Chicago Sweet Connections: Coffee Cake - Blueberry Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0747-2022·2022-03-16
Proton Therapy Systems May Fail to Verify Beam Range After Pause
Proton therapy systems from Ion Beam Applications may not verify that beam range settings remain unchanged after treatment pause, risking incorrect treatment delivery if the range was manually modified.
Product
ProteusPLUS and ProteusONE- designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation Proteus 235
Category
Medical Device
Distribution
12 states
HighFDA (Food)·F-0834-2022·2022-03-16
Chicago Sweet Connections Paczkis Recalled Due to Undeclared Allergens
Chicago Sweet Connections is recalling Cheese Flavor Paczkis due to undeclared allergens: egg, milk, and wheat. The product was distributed to retail locations in Illinois and Wisconsin.
Product
Chicago Sweet Connections: Paczkis - Cheese Flavor packaged in a clear plastic clamshell 4 pack
Category
Food
Distribution
2 states
HighNHTSA·22V163000·2022-03-16
2022 Volkswagen Golf R engine design cover fire risk recall
The engine design cover in 2022 Volkswagen Golf R vehicles may loosen during high acceleration and contact hot engine surfaces, increasing fire risk. Dealers will remove it free of charge.
Product
VOLKSWAGEN — VOLKSWAGEN GOLF R, GTI
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0741-2022·2022-03-16
FISH Diagnostic Probe Kit Color Labeling Error Affects Test Results
Cytocell Ltd. is recalling a Del(5q) Deletion FISH Probe Kit due to incorrect color labeling on probe components. The mislabeling may cause misinterpretation of test results for patients with AML or MDS.
Product
Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML or MDS Catalog Number: USA-LPH024
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0727-2022·2022-03-16
B. Braun dispensing pins recalled for air filter leakage risk
B. Braun Medical is recalling dispensing pins with an elevated leakage risk in the air inlet filter. The leakage may reduce medication doses, delay treatment, or contaminate the fluid path, potentially causing bloodstream infection.
Product
Dispensing Pins for Air Inlet Filter, Product Catalog No. 412005, DP2500 Dispensing Pin W/Valve. A valve for aspiration or injection of medication or enteral feeding solution from inverted multi-dose vials.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0743-2022·2022-03-16
Medtronic endotracheal tubes recalled due to manufacturing nonconformity
Medtronic Xomed is recalling over 301,000 NIM TRIVANTAGE EMG Endotracheal Tubes due to a manufacturing nonconformity. These devices were distributed worldwide.
Product
NIM TRIVANTAGE EMG Endotracheal Tube
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0725-2022·2022-03-16
Philips X-ray System Cooling Leak Poses Fire Risk
Philips Allura CV20 X-ray systems with certain Laird chillers may leak cooling liquid onto electrical components, potentially causing fire or smoke. Affected systems should not be operated until the issue is addressed.
Product
Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without an extended drip tray: Model Number: 722031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0732-2022·2022-03-16
Radiation therapy planning software displays wrong images during animation playback
RayStation/RayPlan versions 6.0.0.24 through 9.2.0.483 incorrectly display selected images as both primary and secondary when animation playback is running, affecting treatment planning visualization.
Product
RayStation/RayPlan- designed for treatment planning and analysis of radiation therapy. Software Version: 6.0.0.24 , 6.1.0.26 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.61 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 , 9.2.0.483 .…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0848-2022·2022-03-16
Pecan Coffee Cake Recalled for Undeclared Allergens: Egg, Milk, Wheat
Chicago Sweet Connections is recalling its Coffee Cake - Pecan Flavor due to undeclared allergens (egg, milk, wheat) not listed on the label. The product was distributed in Illinois and Wisconsin retail locations.
Product
Chicago Sweet Connections: Coffee Cake - Pecan Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0724-2022·2022-03-16
Philips Allura Xper X-ray systems cooling system leak poses fire risk
Philips Allura Xper interventional X-ray systems may experience cooling liquid leaks that could drip on electrical components, creating risk of fire, smoke, or burning odors. No injuries have been reported.
Product
Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System products with a Laird chiller WITHOUT an extended drip tray: Model Number: 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0738-2022·2022-03-16
FDA Recalls Diagnostic Test Strips for False Positive Results
NeuMoDx COVID-19 test strips (Lot 116305 S/L-02) are recalled due to product contamination that increases risk of false positive results. The recall affects 102 boxes distributed in FL, MD, MI, and NY.
Product
NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip, Ref # 300900 (marketed under EUA202947). Distributed in boxes of 6 assay strips in individual pouches. Box, pouch and strips all labeled with product name, ref #, lot #, and expiration date.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0842-2022·2022-03-16
Chicago Sweet Connections Coffee Cake Recalled for Undeclared Egg, Milk, and Wheat Allergens
Chicago Sweet Connections is recalling Apricot Flavor Coffee Cake due to undeclared allergens (egg, milk, and wheat) on the label. The product was distributed to retail locations in Illinois and Wisconsin.
Product
Chicago Sweet Connections: Coffee Cake - Apricot Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
Category
Food
Distribution
2 states
HighFDA (Food)·F-0838-2022·2022-03-16
Chicago Sweet Connections Paczkis Recall: Undeclared Egg, Milk, Wheat Allergens
Chicago Sweet Connections is recalling Prune Flavor Paczkis (4-pack, UPC 841049024035) due to undeclared allergens: egg, milk, and wheat. Affected products were distributed to retail locations in Illinois and Wisconsin.
Product
Chicago Sweet Connections: Paczkis - Prune Flavor packaged in a clear plastic clamshell 4 pack
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0739-2022·2022-03-16
Nextra CH Hammertoe Surgical Implant Kit Recalled for Locking Mechanism Defect
Nextremity Solutions recalls the Nextra CH Hammertoe Mini Instrument Kit for a defect that may deform the implant's locking mechanism during insertion, potentially requiring revision surgery.
Product
Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes SKU: CH-MINI-KT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0845-2022·2022-03-16
Chicago Sweet Connections Coffee Cake Recall Due to Undeclared Allergens
Chicago Sweet Connections is recalling Coffee Cake - Cherry Flavor due to undeclared allergens (egg, milk, and wheat). Affected products were distributed to retail locations in Illinois and Wisconsin.
Product
Chicago Sweet Connections: Coffee Cake - Cherry Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0729-2022·2022-03-16
Vascular Graft Mislabeled; Packaging Labels Do Not Match Product Specifications
A vascular graft has been recalled due to labeling mismatch: the outer package label differs from the inner sterile packaging in graft type and dimensions. Implanting the wrong size could disrupt blood vessel connections and create a pseudo-aneurysm.
Product
HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. Product Code/REF Number: M002020952070
Category
Medical Device
Distribution
Distributed nationwide