State

Illinois product recalls

73,596 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: 2,046
Severe: 3,022
Most recent: 2026-10-24

Of the 11,652 recalls naming Illinois we have scored against our rubric, 2,046 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,022 (26%) are Severe.

Which agencies issued them

These figures cover only the 11,652 recalls whose distribution notice names Illinois specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26326–26350 of 85248

ModerateFDA (Drugs)·D-0068-2022·2021-11-03
Loratadine-D Extended-Release Tablets Recalled for Failed Moisture Limits
Sun Pharmaceutical Industries is recalling 22,752 blister packs of Loratadine-D Extended-Release Tablets (10mg/240mg) distributed nationwide due to failed moisture limits. The affected lot is AC14635 with expiration date 12/2022.
Product
LORATADINE AND PSEUDOEPHEDRINE SULFATE — LORATADINE AND PSEUDOEPHEDRINE SULFATE (LORATADINE AND PSEUDOEPHEDRINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0070-2022·2021-11-03
PainAway II Acetaminophen/Aspirin/Caffeine Tablets Recalled for Failed Stability
Ultra Seal Corporation is recalling PainAway II tablets nationwide due to failed stability specifications. Testing found out-of-specification levels of Salicylic Acid, an aspirin-related compound.
Product
PainAway II (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets , 2 tablets/pk, packaged in 12,000 Packets/Case, Material # 11161, Mfg. for Respond Industries First Aid, Mason, OH 45040 (Shipping Label)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0166-2022·2021-11-03
GORE CARDIOFORM Septal Occluders Recalled for Incorrect Expiration Date
W. L. Gore & Associates is recalling GORE CARDIOFORM Septal Occluders labeled with incorrect 3-year expiration dates instead of 2-year dates. This labeling error affects devices distributed across the United States and internationally.
Product
REF/Catalogue Number GSX0025A, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631025 *Not distributed within the US
Category
Medical Device
Distribution
47 states
ModerateFDA (Food)·F-0088-2022·2021-11-03
Food Grade Calcium Chloride Pellets Recalled for HDPE Contamination
Occidental Chemical Corporation is recalling food grade anhydrous calcium chloride pellets due to potential contamination with fragments of blue high-density polyethylene (HDPE). The recall affects 11,275 bags distributed to food processors and related industries.
Product
Food grade Anhydrous 94-97% Calcium Chloride Pellets, 50 lb. plastic bag
Category
Food
Distribution
5 states
ModerateFDA (Devices)·Z-0167-2022·2021-11-03
GORE CARDIOFORM SEPTAL OCCLUDER Recalled for Incorrect Expiration Date Labeling
GORE CARDIOFORM SEPTAL OCCLUDER devices are recalled for labeling errors: 95 units marked with 3-year expiration instead of correct 2-year date. Affected units distributed across US and international locations.
Product
REF/Catalogue Number GSXE0020, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617630 *Not distributed within the US
Category
Medical Device
Distribution
47 states
LowFDA (Drugs)·D-0072-2022·2021-11-03
ZEE+ Painaid ESF Tablets Recalled for Failed Stability Specifications
Ultra Seal Corporation is recalling ZEE+ Painaid ESF Extra-Strength Formula tablets nationwide due to out-of-specification results for Salicylic Acid, an aspirin-related compound. The recall affects 50-count and 125-count packages with lot numbers AK-9547 (exp. April 22) and AK-9941 (exp. December 22).
Product
ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg, Aspirin 250 mg (NSAID), Caffeine 65 mg) tablets, 2 Tablets per/package, Packaged in a) 50-count packages/carton, b) 125-count packages/carton, PA-ESF 1414Z, Dist. by: Zee Medical Distributors, LLC Mason, OH 45040…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0080-2022·2021-11-03
Rizatriptan Benzoate Orally Disintegrating Tablets Recalled for Out-of-Specification Impurities
Macleods Pharma USA is recalling Rizatriptan Benzoate 10mg orally disintegrating tablets nationwide due to out-of-specification results in organic impurities testing of controlled samples.
Product
RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0069-2022·2021-11-03
Kirkland Signature AllerClear D 24 HR Tablets Recalled for Moisture Failure
SUN PHARMACEUTICAL INDUSTRIES INC is recalling Kirkland Signature AllerClear D 24 HR (Loratadine and Pseudoephedrine Sulfate) tablets nationwide because the product failed to meet moisture content limits.
Product
KIRKLAND SIGNATURE ALLERCLEAR D 24 HR — KIRKLAND SIGNATURE ALLERCLEAR D 24 HR (LORATADINE AND PSEUDOEPHEDRINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0071-2022·2021-11-03
Vica-Cet Back Pain Relief tablets recalled for stability specification failure
Ultra Seal Corporation is recalling Vica-Cet Back Pain Relief tablets nationwide because certain lots failed stability testing and contain out-of-specification levels of Salicylic Acid, an aspirin-related compound.
Product
Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets/pk, packaged in 10,000 packets, PO# 8967, Mfg. for Tellus/The Provision First Aid Line (Shipping Label)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V850000·2021-11-02
Thomas Built Buses Recalling 2020-2022 Models for Alternator Fire Risk
Daimler Trucks is recalling 1,434 Thomas Built school buses because a loose alternator cable connection may cause electrical arcing and increase the risk of a fire.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER EFX
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V848000·2021-11-02
Alfa Romeo Giulia Recalled for Tires with Incorrect Load Rating
FCA US is recalling 2020 Alfa Romeo Giulia vehicles because some may have tires with a lower load rating than intended, increasing crash risk.
Product
ALFA ROMEO — ALFA ROMEO GIULIA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V851000·2021-11-02
Oshkosh Recalls 2020-2021 S-Series Vehicles for Power Steering Defect
Oshkosh is recalling 2020-2021 S-Series vehicles because a machining defect may cause the power steering pump shaft seal to break, resulting in a loss of steering assist.
Product
OSHKOSH — OSHKOSH S-SERIES
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V849000·2021-11-01
Heartland Cyclone and Road Warrior RVs recalled for loose electrical wires
Heartland Recreational Vehicles is recalling 2019-2021 Road Warrior and 2020-2021 Cyclone trailers because wire securement lugs may be improperly tightened. Loose wires can cause electrical arcing and increase fire risk.
Product
HEARTLAND — HEARTLAND CYCLONE, ROAD WARRIOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V844000·2021-10-29
Kia Recalls 2017-2018 Optima Hybrid Vehicles for Engine Bearing Wear
Kia is recalling 2017-2018 Optima Hybrid and Plug-In Hybrid vehicles because premature engine bearing wear can cause engine damage, increasing the risk of fire or a crash.
Product
KIA — KIA OPTIMA HYBRID, OPTIMA PHEV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E092000·2021-10-29
Windshield Fastener Recall: Axalta Coating Systems Bonding Defect
Axalta Coating Systems is recalling windshields that may not be adequately bonded to Ford and Chrysler vehicles due to a coating defect.
Product
VISIBILITY:WINDSHIELD:CRITICAL FASTENERS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V843000·2021-10-29
Mercedes-Benz Recalls 2021 S 580 for Engine Stall Risk
Mercedes-Benz is recalling 2021 S 580 and Maybach S 580 vehicles because a software error may cause the engine to stall without restarting, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ S 580
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V845000·2021-10-29
Thor Motor Coach Recalls 2017 Outlaw, Challenger, and Miramar Motorhomes
Thor Motor Coach is recalling 2017 Outlaw, Challenger, and Miramar motorhomes because external compartment door skins may separate during transit, creating a road hazard.
Product
THOR MOTOR COACH — THOR MOTOR COACH OUTLAW, CHALLENGER, MIRAMAR
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-10292021·2021-10-29
USDA Issues Public Health Alert for Citterio Salame Sticks Due to Salmonella
USDA FSIS issued a public health alert for Citterio Premium Italian-Style Salame Sticks due to possible Salmonella contamination linked to a multistate outbreak.
Product
FSIS Issues Public Health Alert for Salame Stick Products Due to Possible Salmonella Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·21V846000·2021-10-29
Tesla Model 3 Forward Collision Avoidance System Software Error
Tesla is recalling certain 2017-2021 Model 3, S, X, and Y vehicles due to a software error that may cause false forward-collision warnings or unexpected automatic emergency brake activation. No injuries have been reported.
Product
TESLA — TESLA MODEL 3, MODEL X, MODEL S, MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V842000·2021-10-28
2021 Dodge Durango Rear Spoiler May Detach, Becoming Road Hazard
Chrysler is recalling 2021 Dodge Durango vehicles because the rear spoiler may not be properly aligned and could detach during liftgate use, creating a road hazard. Dealers will replace the spoiler free of charge.
Product
DODGE — DODGE DURANGO
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22704·2021-10-28
Design Within Reach Arc Collection Furniture Recalled for Excess Lead Paint
Design Within Reach is recalling its Arc Collection furniture (chairs, tables, and barstools) because the surface paint contains lead levels exceeding the federal lead paint ban, posing a risk of lead poisoning to young children.
Product
Arc Collection Furniture
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21E091000·2021-10-28
American Chrome Company Recalls One Piece Hub Cap Kits for Road Hazard Risk
American Chrome Company is recalling specific One Piece Hub Cap Kits for Volvo and Mack vehicles because a compression spring defect can cause the hubcap to separate, creating a road hazard.
Product
WHEELS:HUBCAP/COVER recall
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0010-2022·2021-10-27
Coppertone Pure & Simple 50 Sunscreen Spray Recalled for Benzene Contamination
Beiersdorf Inc. is recalling Coppertone Pure & Simple 50 Sunscreen Spray due to the presence of benzene, a chemical contaminant. The recall affects 38,328 cans distributed nationwide.
Product
Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02880 0
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0020-2022·2021-10-27
Kalona Supernatural Organic Whipping Cream Recalled for Improper Pasteurization
Kalona Supernatural Organic Whipping Cream was shipped without proper pasteurization, creating a potential food safety risk. The recall affects 16 FL OZ and 32 FL OZ bottles distributed to retailers in multiple states.
Product
Kalona Supernatural Organic Whipping Cream, Manufactured in Iowa for Kalona Organics, LLC. Kalona IA in 16 FL OZ (UPC 8-81245-12016-2, 8 bottles per case) and 32 FL OZ (UPC 8-81245-12032-2, 6 bottles per case)
Category
Food
Distribution
7 states
SevereFDA (Drugs)·D-0012-2022·2021-10-27
Coppertone Pure & Simple Baby Sunscreen Spray Recalled for Benzene Contamination
Beiersdorf Inc. is recalling Coppertone Pure & Simple Baby 50 Sunscreen Spray nationwide due to the presence of benzene, a chemical contaminant. Consumers should stop using affected products immediately.
Product
Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02881 7
Category
Drug
Distribution
Distributed nationwide