State

Illinois product recalls

72,984 recalls have nationwide distribution and so reach Illinois. 11,606 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total: 11,606
Critical: 2,039
Severe: 2,516
Most recent: 2026-09-16

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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6801–6825 of 84590

SevereFDA (Drugs)·D-0493-2025·2025-06-25
UMOVY ACIDO HIALURONICO supplement recalled for undeclared prescription drugs
UMOVY ACIDO HIALURONICO dietary supplement has been recalled because it contains undeclared prescription ingredients Dexamethasone and Diclofenac. The product was marketed without FDA approval.
Product
UMOVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7503046054134
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0053-2025·2025-06-25
Vegetable Bowls and Trays Recalled for Potential Salmonella Contamination
GBC Food Services is recalling vegetable bowls and vegetable ranch trays due to potential Salmonella contamination. Affected products were purchased between May 8 and May 21, 2025.
Product
Vegetable Bowl $5 13oz 850065403380 Purchase Dates: 05/08/2025 to 05/21/2025 Vegetable Bowl $10 26 oz 860010507131 Purchase Dates: 05/08/2025 to 05/21/2025 Vegetable Ranch Tray No Dip Small 19.50 oz 850054894335 Purchase Dates: 05/08/2025 to 05/21/2025 Large Vegetable Tray
Category
Food
Distribution
9 states
SevereNHTSA·25V433000·2025-06-25
Chevrolet Blazer EV parking brake wiring can trigger or lose the brake
General Motors is recalling certain 2024-2025 Chevrolet Blazer EV vehicles because a damaged or corroded rear parking brake harness can activate the parking brake while driving, or disable it while parked.
Product
CHEVROLET — CHEVROLET BLAZER EV
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1943-2025·2025-06-25
Dexcom G6 Glucose Receiver recalled for missed audible alerts
Dexcom G6 Glucose Receiver units may have defective foam or assembly errors that disable audible alerts for dangerously low or high blood glucose, risking seizures, loss of consciousness, or death.
Product
Dexcom G6 Glucose Receiver, SKUs (Part Number): STK-FM-001 (MT27408-1) & STK-FR-001 (MT27408-1)
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V414000·2025-06-25
International CV brake pressure sensor can leak fluid causing fire
International is recalling certain 2019-2025 CV vehicles because the brake pressure sensor assembly may leak brake fluid into the pressure switch and short circuit. Owners are advised to park outside until repaired.
Product
INTERNATIONAL — INTERNATIONAL CV
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-0052-2025·2025-06-25
Cucumber bowls and snack cups recalled due to Salmonella contamination risk
GBC Food Services, LLC is recalling cucumber products sold between May 8 and May 21, 2025, due to potential Salmonella contamination. Affected products include Cucumber Bowl with Ranch dip, Cucumber Slices with Tajin, and Cucumber with Ranch Snack Cup.
Product
Cucumber Bowl with Ranch dip 15oz UPC 850054894519 Purchase Dates: 05/08/2025 to 05/21/2025 Cucumber Slices W/Tajin 10 oz UPC 85005368569 Purchase Dates: 05/08/2025 to 05/21/2025 Cucumber w/ Ranch Snack Cup 9.5 oz UPC 850065403144 Purchase Dates: 05/08/2025 to 05
Category
Food
Distribution
9 states
HighFDA (Devices)·Z-1985-2025·2025-06-25
Surgical Mesh Recalled for Potential Residual Adhesive Material
Chamberlain Technologies LLC is recalling SURGIMESH XB surgical mesh due to potential residual adhesive material on the mesh surface. The affected product was distributed to Illinois, Nebraska, and California.
Product
SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-1992-2025·2025-06-25
Fresenius 5008X HDF Hemodialysis Blood Tubing Sets recalled for potential blood leaks
Fresenius Medical Care is recalling 5008X HDF Hemodialysis Blood Tubing Sets due to potential blood leaks between the venous chamber and tubing. The recall affects hemodialysis, hemodiafiltration, hemofiltration, and isolated ultrafiltration procedures nationwide.
Product
5008X HDF Hemodialysis Blood Tubing Set, 24 units per case, with the following models: a. 5008X Standard HDF Bloodline, Model Number: 03-5100-7. b. 5008X Standard HDF Bloodline w/CLIC, Model Number: 03-5100-7C. c. 5008X Standard HDF Bloodline w/ Twister, Model Number: 03-5150-
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1981-2025·2025-06-25
UROSKOP Omnia X-ray System Model 10094910 Frequency Inverter Overheating Recall
Siemens is recalling 95 units of the UROSKOP Omnia X-ray system nationwide due to a resistor in the frequency inverter that may overheat and potentially ignite the plastic housing.
Product
UROSKOP Omnia. Model Number: 10094910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1991-2025·2025-06-25
ICU Medical Plum Solos Infusion Pump Software Safety Defect Recall
ICU Medical is recalling Plum Solos infusion pumps (Item 400011001) with software version 1.1.1 due to a workflow that may bypass the Maximum Dose Limit alert, which is designed to prevent overdose. The defect affects 214 units distributed across nine US states and the Philippines.
Product
ICU Medical Plum Solos, Item number 400011001; infusion pump
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1990-2025·2025-06-25
ICU Medical Plum Duo Infusion Pump Software Dose Limit Issue
ICU Medical is recalling Plum Duo infusion pumps with software version 1.1.1 because a workflow may bypass the Maximum Dose Limit alert, potentially allowing unsafe medication doses to be programmed.
Product
ICU Medical Plum Duo, Item numbers: 1) 400020401, 2) 400021001 , and 3) 400021003; infusion pump
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1987-2025·2025-06-25
Biomet 3i Certain-Compatible 4.1mm Milled Titanium Dental Abutments
Preat Corp is recalling Biomet 3i Certain-compatible 4.1mm Milled Titanium Abutments (Model 9001767-F) due to manufacturing defects that may cause improper screw engagement. The screw seat was positioned too high, potentially compromising the attachment of mating screws to the underlying implant.
Product
Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1980-2025·2025-06-25
Portable Oxygen Concentrator with Erroneous Calibration Values
Ohio Medical Corporation is recalling 36 units of the GCE HEALTHCARE Zen-O lite portable oxygen concentrator due to erroneous calibration values that may cause the device's alarm for low oxygen purity to function incorrectly as the device ages.
Product
GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1982-2025·2025-06-25
Siemens UROSKOP Omnia Max frequency inverter fire risk recalled
Siemens is recalling UROSKOP Omnia Max medical devices due to a resistor in the frequency inverter that may overheat and ignite the plastic housing. Twenty-five units distributed nationwide are affected.
Product
UROSKOP Omnia Max. Model Number: 10762473
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0055-2025·2025-06-25
Fruit and Veg Tray 64oz Recalled for Potential Salmonella Contamination
GBC Food Services, LLC is recalling Fruit and Veg Tray 64oz products due to potential Salmonella contamination. The affected products were distributed to multiple states and purchased between May 8 and May 21, 2025.
Product
Fruit and Veg Tray 64oz 850065403748 Purchase Dates: 05/08/2025 to 05/21/2025
Category
Food
Distribution
9 states
HighFDA (Devices)·Z-1988-2025·2025-06-25
Optima Coil System embolization coils recalled for defective radiopaque marker
BALT USA is recalling the Optima Coil System because the radiopaque marker was not visible during angiography and was not manufactured to specification.
Product
Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851 OPTI0258BLK 00810068568929 OPTI0212BLK 00810068568912 OPTI0206BLK 00810068568905 OPTI0310BLK 00810068568943 OPTI0320BLK 00810068568950 OPTI0151HSS10 008
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0050-2025·2025-06-25
Great Plains Bentonite Herbal Detox Capsules Recall
Yerba Prima Inc is recalling Great Plains Bentonite + Herbal Detox Capsules due to potential contamination with Pseudomonas aeruginosa. Affected bottles have Lot # 05051 with expiration date 02/2028.
Product
Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper proof seal. Case GTIN code:100 46352 00518 5. Retail package UPC code: 0 46352 00518 8. Yerba Prima, Inc. 740 Jefferson Ave Ashland, Oregon 97520 USA
Category
Food
Distribution
21 states
HighFDA (Devices)·Z-1989-2025·2025-06-25
Prestige Coil System implantable devices recalled for manufacturing defect
BALT USA is recalling Prestige Coil System implantable embolization devices because radiopaque markers on some units were not manufactured to specification and were not visible during angiography.
Product
Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT 00810068567663 PRES1245CPKPLT 00810068567694 PRES1445CPKPLT 00810068567724 PRES0103CXPPLT 00810068567304 PRES2512CXPPLT 00810068567397 PRES0258CXPPLT 00810068567380 PRES0212CXPPLT 0081006
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1986-2025·2025-06-25
Surgical Mesh Recalled Due to Residual Adhesive Material Concern
Chamberlain Technologies LLC is recalling SURGIMESH WN polymeric surgical mesh due to potential residual adhesive material on the mesh surface. The recall affects 20 units distributed to Illinois, Nebraska, and California.
Product
SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog Number: T1415
Category
Medical Device
Distribution
3 states
ModerateFDA (Drugs)·D-0472-2025·2025-06-25
Gentamicin Injection Pediatric Vials Recalled for Failed Stability Tests
Eugia US LLC is recalling Gentamicin Injection, USP (Pediatric), 20 mg per 2 mL due to failed color absorbance test results during 12-month stability analysis. The recall affects 48,000 vials distributed nationwide.
Product
GENTAMICIN — GENTAMICIN (GENTAMICIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1978-2025·2025-06-25
MiniDock Integrated Nucleic Acid Testing Device Recall
Guangzhou Pluslife Biotech is recalling the MiniDock Integrated Nucleic Acid Testing Device (Model PM001) because it was distributed in the U.S. without required FDA premarket authorization.
Product
Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device Model/Catalog Number: PM001 Software Version: N/A Product Description: 1. Product Overview 1.1 Product Name: Integrated Nucleic Acid Testing Device Brand Name: MiniDock 1.2 Model: PM001 2.Pr
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1984-2025·2025-06-25
Surgical Mesh Product Recalled Due to Residual Adhesive Material
Chamberlain Technologies is recalling SURGIMESH XB surgical mesh due to potential residual adhesive material on the mesh surface. The product was distributed to facilities in Illinois, Nebraska, and California.
Product
SURGIMESH XB, Polymeric Surgical Mesh, 14m x 15cm Flat Sheet with Silicone Barrier, Model/Catalog Number: Tintra R-1415
Category
Medical Device
Distribution
3 states
ModerateFDA (Devices)·Z-1983-2025·2025-06-25
Surgical Mesh Recalled for Potential Residual Adhesive Material
Chamberlain Technologies LLC is recalling SURGIMESH WN Polymeric Surgical Mesh due to potential residual adhesive material on the mesh surface. The 60-unit recall affects medical facilities in Illinois, Nebraska, and California.
Product
SURGIMESH WN, Polymeric Surgical Mesh, Large Flat Sheet, Model/Catalog Number: T3030
Category
Medical Device
Distribution
3 states
ModerateFDA (Drugs)·D-0471-2025·2025-06-25
Amazon Basic Care Acetaminophen 325 mg Tablets Recalled Due to Discoloration
Aurobindo Pharma USA Inc is recalling Amazon Basic Care Acetaminophen 325 mg tablets due to confirmed consumer complaints of brown surface discoloration on tablets, a cGMP deviation.
Product
AMAZON BASIC CARE ACETAMINOPHEN — AMAZON BASIC CARE ACETAMINOPHEN (ACETAMINOPHEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1979-2025·2025-06-25
Pluslife SARS-CoV-2 Card Test Kits Recalled for Lack of FDA Authorization
Pluslife SARS-CoV-2 Card nucleic acid testing kits were distributed in the U.S. without required FDA premarket authorization. The FDA is recalling approximately 1,850 boxes distributed nationwide and internationally.
Product
Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid Testing Card Model/Catalog Number: RM1010202 Software Version: N/A Product Description: 1. Product Overview Product Name: SARS-CoV-2 Nucleic Acid Testing Card Trade Name: Pluslife SARS-CoV-2 Card 2
Category
Medical Device
Distribution
Distributed nationwide