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.

701–725 of 84421

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 (Drugs)·D-0684-2026·2026-07-22
Good Neighbor Pharmacy Earwax Removal Drug Recalled for Low Potency
Bell Pharmaceuticals is recalling Good Neighbor Pharmacy Earwax Removal (Carbamide Peroxide 6.5%) due to subpotency—the active ingredient concentration is significantly reduced from expected levels, and the product has a low pH.
Product
GOOD NEIGHBOR PHARMACY EARWAX REMOVAL — GOOD NEIGHBOR PHARMACY EARWAX REMOVAL (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 (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 (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-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-0686-2026·2026-07-22
Foster & Thrive Carbamide Peroxide 6.5% Recalled for Subpotent Strength
Bell Pharmaceuticals recalls Foster & Thrive Carbamide Peroxide 6.5% due to subpotent drug substance with low pH and significantly reduced assay levels. Approximately 31,094 units distributed nationwide are affected.
Product
Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141.
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 (Devices)·Z-2722-2026·2026-07-22
da Vinci SP Instrument Arm Drape may detach during surgical procedures
Intuitive Surgical is recalling da Vinci SP Instrument Arm Drapes because the drape rings may detach, exposing the instrument arm and potentially delaying procedures. The recall affects 11,113 units distributed worldwide.
Product
da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0677-2026·2026-07-22
Nystatin Cream Recall Due to Low Potency Test Results
Padagis US LLC is recalling Nystatin Cream USP (100,000 USP units) because long-term stability testing found assay results below specification, meaning the product may contain less active ingredient than labeled.
Product
NYSTATIN — NYSTATIN (NYSTATIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0680-2026·2026-07-22
Quality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall
Bell Pharmaceuticals is recalling Quality Choice Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotent drug content, with assay levels significantly reduced (approximately 0.6% versus expected 6–7%) and low pH levels.
Product
QUALITY CHOICE EARWAX REMOVAL KIT — QUALITY CHOICE EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
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
LowFDA (Devices)·Z-2740-2026·2026-07-22
Rio II Nasal Pillows Interface Packaging and Labeling Discrepancy Recall
3B Medical, Inc. is recalling Rio II Nasal Pillows Interface devices due to packaging and labeling discrepancies involving product size identification and device identifiers. The affected models are RII1001 (Small), RII1002 (Medium), and RII1003 (Large).
Product
Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number: RII1001 (Small), RII1002 (Medium), RII1003 (Large) Software Version: N/A Product Description: Nasal pillows interface intended for use with positive airway pressure therapy devices. The de
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V470000·2026-07-21
Ford Recalls 2025-2027 Explorer and Lincoln Aviator for Seat Recline Issue
Ford is recalling 76,748 2025-2027 Explorer and Lincoln Aviator vehicles because an unoccupied driver's seat may recline unintentionally, potentially trapping a second-row occupant.
Product
FORD — FORD, LINCOLN EXPLORER, AVIATOR
Category
Vehicle
Distribution
Distributed nationwide
LowNHTSA·26V469000·2026-07-21
Ember Recalls 2027 Travel Trailers Due to Incorrect VIN Labels
Ember is recalling 2027 E-Series, Touring, and Overland travel trailers because the Federal Certification Label may list the wrong VIN, which could prevent owners from recognizing safety recalls.
Product
EMBER — EMBER E-SERIES, TOURING EDITION, OVERLAND SERIES
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V467000·2026-07-20
Blue Bird Recalls 2022-2027 Vision Transit Buses for Brake Line Damage
Blue Bird is recalling 2022-2027 Vision transit buses because an exhaust hanger pin may damage the hydraulic brake line, causing leaks and increasing fire or crash risks.
Product
BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V466000·2026-07-20
Blue Bird Vision School Buses Recalled Due to Brake Line Fire and Crash Risk
Blue Bird is recalling certain 2022-2027 Vision school buses because an exhaust hanger cotter pin may damage hydraulic brake lines, causing leaks that increase the risk of fire or crashes.
Product
BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V468000·2026-07-20
Ford Bronco and Bronco Raptor vehicles recalled due to engine compartment fire risk
Ford Motor Company is recalling certain 2021-2026 Bronco and Bronco Raptor vehicles because the engine compartment wiring harness may short circuit and cause a fire.
Product
FORD — FORD BRONCO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V463000·2026-07-17
Altec Recalls 2024-2026 AT Series Vehicles Due to Bearing Fastener Defect
Altec is recalling 2024-2026 AT Series vehicles because turntable rotation bearing fasteners may not have been heat treated properly, posing a risk of component separation and injury.
Product
ALTEC — ALTEC AT SERIES
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V462000·2026-07-17
Turtle Top Recalls 2026 Terra Ford Transit Buses Due to Lift Control Failure
Turtle Top is recalling 2026 Terra Ford Transit buses because an electrical contactor may fail, preventing the wheelchair lift from stopping. This defect increases the risk of injury.
Product
TURTLE TOP — TURTLE TOP TERRA FORD TRANSIT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V464000·2026-07-17
Foretravel Recalls 2027 Realm Motorcoaches Due to Fire Risk
Foretravel is recalling 2027 Realm Presidential Motorcoaches because a fan assembly circuit board may overheat, increasing the risk of a fire.
Product
FORETRAVEL — FORETRAVEL REALM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26C004000·2026-07-17
Evenflo Recalls Reo by Revolve360 Child Seats for Headrest Shift Risk
Evenflo is recalling specific Reo by Revolve360 child seats because the headrest may shift during a crash, increasing injury risk.
Product
CHILD SEAT:SHELL:HEADREST:LOCKING MECHANISM recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·26V465000·2026-07-17
Great Dane Recalls 2027 Champion Trailers for Rear Impact Guard Defect
Great Dane is recalling 2027 Champion dry van trailers because they may lack required rear impact guard extension channels, increasing injury risk in crashes.
Product
GREAT DANE — GREAT DANE CHAMPION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V460000·2026-07-16
IC Bus EVSB and CESB school buses recalled for structural body joint defects
International Motors, LLC is recalling certain 2025-2027 IC Bus EVSB and CESB school buses due to insufficient epoxy coverage on body joints. This defect may cause panels to separate during a crash.
Product
IC BUS — IC BUS CESB, EVSB
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V457000·2026-07-16
Altec Recalls AP Series Trucks Due to Fire Risk
Altec is recalling 2013-2025 AP45A trucks because a damaged wire in the cargo area can overheat and ignite flammable material, increasing the risk of fire.
Product
ALTEC — ALTEC AP SERIES
Category
Vehicle
Distribution
Distributed nationwide