State

Illinois product recalls

72,820 recalls have nationwide distribution and so reach Illinois. 11,601 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total: 11,601
Critical: 2,039
Severe: 2,514
Most recent: 2026-09-06

Of the 11,601 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 2,514 (22%) are Severe.

Which agencies issued them

These figures cover only the 11,601 recalls whose distribution notice names Illinois specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

676–700 of 84421

HighFDA (Devices)·Z-2741-2026·2026-07-22
Vasoview Hemopro 2 Endoscopic Vessel Harvesting System Recall
Maquet Cardiovascular is recalling Vasoview Hemopro 2 devices from Lot 3000547797 due to exposure to out-of-specification sterilization during gamma sterilization. The affected devices may not be properly sterilized.
Product
The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2727-2026·2026-07-22
GE Optima XR200/220/240amx Radiographic System Column Safety Mechanism
GE Medical Systems is recalling certain Optima XR200/220/240amx mobile radiographic systems after column replacements because functional testing of the safety pawl may not have been performed, which could allow the X-ray arm to drop and injure patients.
Product
Optima XR220amx, Mobile Digital-Ready Radiographic System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2730-2026·2026-07-22
Orthofix MINIRAIL external fixation devices recalled for incorrect labeling
Orthofix U.S. LLC is recalling 19 units of Orthofix MINIRAIL orthopedic external fixation devices distributed across the US due to incorrect model labeling that could lead to surgical use of the wrong device.
Product
Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral orthopedic/trauma external fixation device
Category
Medical Device
Distribution
26 states
HighNHTSA·26E047000·2026-07-22
Hiab Recalls K-HiPro Cranes Due to Potential Column Weld Failure
Hiab USA Inc. is recalling K-HiPro 425 and 505 cranes because a weld may crack, risking column collapse and injury.
Product
EQUIPMENT:MECHANICAL:BOOM/CRANE/LADDER recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2725-2026·2026-07-22
Rapid Refill Continuous Injection System Recalled for Syringe Loosening Risk
Boston Scientific's Rapid Refill Continuous Injection System (UPN M00566001) is being recalled because the recalled Medline Namic Angiographic Control Syringe may loosen or disconnect from the manifold, potentially causing leakage, inability to aspirate or inject, and procedure delays.
Product
Rapid Refill Continuous Injection System, UPN M00566001
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V475000·2026-07-22
Freightliner Trucks Recalled for Low Beam Headlight Software Error
Daimler Trucks North America is recalling 2026-2027 Freightliner models because a software error may cause low beam headlights to illuminate improperly, increasing crash risk.
Product
FCCC — FCCC, FREIGHTLINER S2C, S2RV, BUSINESS CLASS M2, EM2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2728-2026·2026-07-22
Mobile Digital Radiographic System Arm Drop Risk During Patient Exams
GE HealthCare is recalling certain Optima XR200/220/240amx Mobile Digital Radiographic Systems due to potential failure of the Column Safety mechanism, which could cause the X-ray arm to drop during patient exams. The issue stems from incomplete functional testing of the safety pawl after column replacement.
Product
Optima XR240amx, Mobile Digital Radiographic System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2718-2026·2026-07-22
Olympus Toomey Evacuator 30cc medical device sterilization parameters recalled
Olympus Corporation recalled the Toomey Evacuator 30cc with Adaptor (Model 188) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.
Product
Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V471000·2026-07-22
ATC Recalls 2026 RM500 and RM700 Trailers Due to Winch Remote Issue
Aluminum Trailer Company is recalling 2026 RM500 and RM700 trailers because the wireless remote may cause unexpected winch movements, increasing injury risk.
Product
ATC — ATC RM500, RM700
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V473000·2026-07-22
2024–2026 Volkswagen Atlas and Atlas Cross Sport Rearview Camera Software
Volkswagen is recalling 2024–2026 Atlas and Atlas Cross Sport vehicles due to a low-voltage electrical event that may cause the rearview camera display to fail, reducing rear visibility.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0678-2026·2026-07-22
CVS Health Earwax Removal Drops Recalled for Subpotent Active Ingredient
CVS Health Earwax Removal Drops are being recalled because the product contains significantly reduced active ingredient (approximately 0.6% instead of the expected 6–7%) and has low pH. The recalled product may not work as intended.
Product
CVS HEALTH EARWAX REMOVAL DROPS EARWAX REMOVAL AID — CVS HEALTH EARWAX REMOVAL DROPS EARWAX REMOVAL AID (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2736-2026·2026-07-22
Medline Kits with Zimmer Biomet Mixing Bowls Recalled for Seal Defects
Medline is recalling 163 kits containing Zimmer Biomet mixing bowls and spatulas due to seal nonconformities that may compromise sterility. The defect could require extended surgery time to locate an alternative device.
Product
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0685-2026·2026-07-22
Leader Carbamide Peroxide Earwax Removal Kit Recalled for Subpotency
Bell Pharmaceuticals is recalling Leader Carbamide Peroxide 6.5% Earwax Removal Kit due to subpotency—the active ingredient is significantly reduced (approximately 0.6% versus the expected 6–7%) and the pH is low.
Product
LEADER EARWAX REMOVAL KIT EARWAX REMOVAL AID AND BULB — LEADER EARWAX REMOVAL KIT EARWAX REMOVAL AID AND BULB (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2734-2026·2026-07-22
Papablic Replacement Brush Heads Recalled Due to Breakage Risk
Papablic Inc is recalling Papablic Replacement Brush Heads (Model PAPA317AA) due to potential for brush heads to break. The recall affects approximately 13,400 packs distributed nationwide.
Product
Papablic Replacement Brush Heads. Model Number: PAPA317AA.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2746-2026·2026-07-22
Tosoh ST AIA-Pack Testosterone Diagnostic Test Kit Recall
Tosoh Bioscience is recalling ST AIA-Pack Testosterone test kits due to low-quality control results that could produce falsely elevated or falsely low testosterone measurements, potentially leading to unnecessary testing or delayed diagnosis.
Product
ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers, Model Number 0025204
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2742-2026·2026-07-22
Photera 400 Phototherapy Device Recalled for Incorrect UV Sensor Calibration
Daavlin Distributing Company is recalling the Photera 400 phototherapy device because the UV sensor calibration is calculating incorrectly, resulting in lower output levels than intended.
Product
Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0687-2026·2026-07-22
Meijer Earwax Removal Kit Recalled for Subpotent Active Ingredient
Bell Pharmaceuticals is recalling Meijer Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotency: the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, limiting effectiveness.
Product
MEIJER EARWAX REMOVAL KIT — MEIJER EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0681-2026·2026-07-22
TopCare Earwax Removal Kit Recalled for Subpotent Drug Content
Bell Pharmaceuticals is recalling TopCare Earwax Removal Kit (Carbamide Peroxide 6.5%) because the drug is subpotent with significantly reduced active ingredient (~0.6% vs. expected 6–7%) and low pH. The affected product was distributed nationwide.
Product
TOPCARE EARWAX REMOVAL KIT — TOPCARE EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2729-2026·2026-07-22
Orthofix MINIRAIL external fixation devices recalled for incorrect model labeling
Orthofix U.S. LLC is recalling Orthofix MINIRAIL external fixation devices (Model M101) because they may be labeled with incorrect model numbers, potentially leading to use of wrong device specifications.
Product
Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device
Category
Medical Device
Distribution
26 states
ModerateFDA (Drugs)·D-0679-2026·2026-07-22
Clinere Ear Wax Remover Recalled for Subpotent Carbamide Peroxide
Bell Pharmaceuticals is recalling Clinere Ear Wax Remover nationwide because the product contains significantly reduced active ingredient and low pH. The affected lots were distributed throughout the United States.
Product
CLINERE EAR WAX REMOVER — CLINERE EAR WAX REMOVER (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0682-2026·2026-07-22
Audiologist's Choice Carbamide Peroxide Earwax Removal Recalls
Bell Pharmaceuticals is recalling Audiologist's Choice Carbamide Peroxide earwax removal product due to subpotency: the active ingredient concentration is approximately 0.6% instead of the expected 6–7%, and the product has low pH.
Product
AUDIOLOGISTS CHOICE EARWAX REMOVAL SYSTEM — AUDIOLOGISTS CHOICE EARWAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1152-2026·2026-07-22
Liquid Hope Organic Meal Replacement Formula Subpotent Vitamin A Recall
Nutricia North America is recalling Liquid Hope Organic Whole Foods Meal Replacement Peptide Formula Berry Medley because the product contains less vitamin A than labeled. A testing laboratory used an incorrect method that overstated the vitamin A concentration.
Product
functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ (341g) case UPC 8 57858 00453 3, package UPC 8 57858 00450 2
Category
Food
Distribution
49 states
ModerateFDA (Devices)·Z-2737-2026·2026-07-22
Medline Kits with Zimmer Biomet Mixing Bowls and Spatulas Recalled
Medline Industries is recalling 163 kits containing Zimmer Biomet mixing bowls and spatulas due to seal defects that risk sterility breach during surgical procedures.
Product
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1174-2026·2026-07-22
Amy's Organic Lentil Soup Recalled for Potential Spoilage Risk
Amy's Kitchen is recalling Amy's Organic Soups Lentil Light in Sodium (14.5 oz cans) due to potential for spoilage. The recall affects approximately 15,350 cases distributed across multiple U.S. states and Canada.
Product
Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl. Cover. Cook for 1.5-2 minutes. Let sit 1 minute. Stir. Serve. Stovetop: Heat soup in a saucepan, stirring occasionally. AMY'S KITCHEN, INC. P.O. BOX 7129 PETAL
Category
Food
Distribution
28 states
ModerateFDA (Devices)·Z-2744-2026·2026-07-22
Photera 600 3-D phototherapy device UV sensor calibration error recall
Daavlin Distributing Company is recalling Photera 600 3-D phototherapy devices because the UV sensor gain calculation is incorrect, causing inaccurate ultraviolet output measurement.
Product
Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Category
Medical Device
Distribution
Distributed nationwide