State

Illinois product recalls

73,388 recalls have nationwide distribution and so reach Illinois. 11,648 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total: 11,648
Critical: 2,050
Severe: 3,017
Most recent: 2026-10-07

Of the 11,648 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 3,017 (26%) are Severe.

Which agencies issued them

These figures cover only the 11,648 recalls whose distribution notice names Illinois specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18176–18200 of 85036

ModerateFDA (Food)·F-0952-2023·2023-05-31
Culinaria Cashew and Macadamia Mix Recalled for Label Mix-Up
Culinaria Branded Roasted & Salted Colossal Cashew & Macadamia Mix (828 cans, Lot 3033A9) is being recalled due to a label mix-up. The product was distributed in Illinois, Indiana, and Missouri.
Product
Culinaria Branded Roasted & Salted Colossal Cashew & Macadamia Mix. Net Wt 9oz (255g) UPC 0 41318-22428 3. Distributed by Schnuck Markets, Inc., St. Louis, MO 63146-6928.
Category
Food
Distribution
3 states
ModerateFDA (Drugs)·D-0768-2023·2023-05-31
Fentanyl Buccal Tablets 400mcg missing or incorrect package insert
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets 400mcg due to incorrect or missing package inserts in affected cartons distributed nationwide. No illnesses have been reported.
Product
Fentanyl Buccal Tablets CII, 400mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-636-28
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0759-2023·2023-05-31
Glimepiride 4 Milligram Tablets Nationwide Recalled for Manufacturing Practice Deviations
Amerisource Health Services LLC is recalling 129,849 bottles of Glimepiride Tablets, USP 4 mg nationwide due to manufacturing practice deviations identified during an FDA inspection. No illnesses have been reported.
Product
Glimepiride Tablets, USP, 4 mg, RX, Packaged as a) 100-count bottle, NDC# 68001-179-00; b) 500-count bottle, NDC# 68001-179-03, Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213. INDIA. For BluePoint Laboratories
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0940-2023·2023-05-31
Dietary Supplement TruCONTROL Recalled Due to Unapproved Ingredients
TruVision Health's truCONTROL 60 Count dietary supplement is being recalled because it contains DMHA and/or hordenine, which the FDA has determined are not acceptable dietary ingredients.
Product
truCONTROL 60 Count
Category
Food
Distribution
50 states
ModerateFDA (Food)·F-0944-2023·2023-05-31
Dietary Supplement Recall: TruWeight and Energy Gen 2+ Contains Banned Ingredients
TruVision Health is recalling TruWeight and Energy Gen 2+ because it contains DMHA and hordenine, which FDA has determined are not acceptable dietary ingredients. No illnesses have been reported.
Product
TruWeight and Energy Gen 2+ 60 Count
Category
Food
Distribution
50 states
ModerateFDA (Food)·F-0943-2023·2023-05-31
Dietary supplement recalled for containing unapproved ingredients
TruVision Health LLC is recalling truControl W/Dynamine because the product contains DMHA and/or hordenine, which FDA has determined are not acceptable dietary ingredients.
Product
truControl W/Dynamine 60 ct
Category
Food
Distribution
50 states
ModerateFDA (Devices)·Z-1479-2023·2023-05-31
Fluoroscopic imaging system may display incorrect radiation dose readings
Siemens Luminos Agile Max fluoroscopic imaging systems may occasionally display incorrect radiation dose information under certain unlikely circumstances. The manufacturer states there is no impact on clinical workflow or diagnosis. The error only occurs in systems with a second overhead X-ray tube.
Product
Luminos Agile Max (VE10, VF10, VF11)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1632-2023·2023-05-31
Siemens Atellica CH Toxicology Calibrator Reassignment Due to Positive Bias
Siemens Healthcare Diagnostics is reassigning Atellica CH Toxicology Calibrators due to a positive bias. The affected calibrators were distributed in the US and internationally across multiple countries.
Product
Atellica CH Toxicology Calibrator (TOX CAL)-The Atellica¿ CH Toxicology Calibrator (TOX CAL) is for in vitro diagnostic use in calibrating the Acet, ETOH and Sal assays using the Atellica¿ CH Analyzer Siemens Material Number (SMN): 11099440
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0767-2023·2023-05-31
Fentanyl Buccal Tablets Recalled for Missing or Incorrect Package Insert
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets (200mcg) due to missing or incorrect package inserts. Patients should contact their healthcare provider if they have affected product.
Product
Fentanyl Buccal Tablets CII, 200mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-635-28
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1480-2023·2023-05-31
Fluoroscopic Imaging System May Display Incorrect Radiation Dose Measurements
Siemens Luminos dRF Max fluoroscopic imaging systems may occasionally display incorrect radiation dose measurements during certain operating conditions. The manufacturer states the error does not affect diagnosis or workflow.
Product
Luminos dRF Max (VE10, VF10, VF11)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1481-2023·2023-05-31
LUMINOS Lotus Max fluoroscopic system recalled for sporadic measurement errors
LUMINOS Lotus Max fluoroscopic systems may sporadically display incorrect radiation dose measurements. The error only occurs with secondary X-ray tubes and does not affect diagnosis or workflow.
Product
LUMINOS Lotus Max (VF11)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0757-2023·2023-05-31
Nationwide Recall of Glimepiride Tablets for Manufacturing Practice Deviations
Amerisource Health Services LLC recalls 63,335 bottles of Glimepiride Tablets nationwide due to manufacturing practice deviations identified during FDA inspection.
Product
Glimepiride Tablets, USP, 1 mg, RX, Packaged as a)100-count bottle, NDC# 68001-177-00; b) 500-count bottle, NDC# 68001-177-03; Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213. INDIA. For BluePoint Laboratories
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0770-2023·2023-05-31
Fentanyl buccal tablets recalled due to incorrect or missing package insert
Teva Pharmaceuticals USA Inc is recalling Fentanyl Buccal Tablets 800mcg due to incorrect or missing package inserts. The recall affects 3,032 units distributed nationwide.
Product
Fentanyl Buccal Tablets CII, 800mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-638-28
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0766-2023·2023-05-31
Fentanyl Buccal Tablets recalled due to missing or incorrect package insert
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets 100mcg due to incorrect or missing package inserts in affected cartons. Patients should verify proper labeling or contact their pharmacy.
Product
Fentanyl Buccal Tablets CII, 100mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-634-28
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0769-2023·2023-05-31
Fentanyl Buccal Tablets 600mcg Recalled for Incorrect or Missing Package Insert
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets 600mcg due to incorrect or missing package inserts in 1,908 units distributed nationwide across multiple lot numbers.
Product
Fentanyl Buccal Tablets CII, 600mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-637-28
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0756-2023·2023-05-31
Methylprednisolone Acetate Injectable Suspension recalled for NDC carton labeling error
Amneal Pharmaceuticals recalls Methylprednisolone Acetate Injectable Suspension due to incorrect NDC number on product cartons. The typographical error appears on secondary packaging only; the medication vial itself is unaffected.
Product
Methylprednisolone Acetate Injectable Suspension, USP 80 mg/mL, For Intramuscular, Intrasynovial and Soft Tissue Injection Only, Not for Intravenous Use, 1 mL Single Dose Vial, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Parenteral Unit, Ahmedabad 382213, India, Amneal…
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·23V383000·2023-05-30
Wabash National Recalls 2024 Dry Van Trailers Due to King Pin Weld Defect
Wabash National is recalling 2024 DVDBHPC and DVCVHPC dry van trailers because improperly welded king pins may detach, increasing crash risk.
Product
WABASH NATIONAL — WABASH NATIONAL DRY VAN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V382000·2023-05-30
Alfa Romeo Giulia and Stelvio Recalled for Brake Rotor Fracture Risk
NHTSA is recalling 2017-2020 Alfa Romeo Giulia and 2018-2020 Stelvio vehicles with carbon ceramic brakes due to a risk of rotor fracture and decreased brake performance.
Product
ALFA ROMEO — ALFA ROMEO STELVIO, GIULIA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V384000·2023-05-30
2023 Toyota Corolla Cross instrument panel airbag deployment risk
Toyota is recalling 2022-2023 Corolla Cross vehicles because the instrument panel may lack required perforations, preventing proper front-passenger airbag deployment in a crash.
Product
TOYOTA — TOYOTA COROLLA CROSS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V385000·2023-05-30
Tesla Recalls 2022-2023 Model Y Vehicles for Loose Steering Wheel Fastener
Tesla is recalling 2022-2023 Model Y vehicles because a loose steering wheel fastener may allow the wheel to disconnect, increasing crash risk.
Product
TESLA — TESLA MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V378000·2023-05-26
Ford Recalls 2015-2019 Lincoln MKC for Engine Compartment Fire Risk
Ford is recalling 2015-2019 Lincoln MKC vehicles because a battery monitor sensor may short-circuit and overheat, causing a fire in the engine compartment.
Product
LINCOLN — LINCOLN MKC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V375000·2023-05-26
Forest River Recalls 2023 East to West Travel Trailers Due to Gas Leak Risk
Forest River is recalling 2023 East to West Della Terra and Silver Lake travel trailers because an incorrectly installed furnace may cause a gas leak inside the cabin.
Product
EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V381000·2023-05-26
Knapheide Recalls Vehicles with Warn Winches Due to Unintentional Operation Risk
Knapheide is recalling 2022-2023 trucks equipped with certain Warn winches because water intrusion can cause the winch to operate unintentionally, increasing injury risk.
Product
KNAPHEIDE — KNAPHEIDE RAM 3500, FORD F-350, FORD F-250, FORD F-550
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V380000·2023-05-26
Ford Escape, Maverick, and Corsair Engine Fire Risk Recall
Ford is recalling certain 2020-2023 Escape, 2022-2023 Maverick, and 2021-2023 Corsair vehicles due to a 2.5L engine defect that could cause an engine compartment fire. No injuries have been reported.
Product
FORD — FORD, LINCOLN MAVERICK, CORSAIR, ESCAPE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V379000·2023-05-26
Ford Vehicles Recalled for Incorrect Tire and Loading Capacity Label
Ford is recalling certain 2019-2023 Ranger, 2022-2023 Bronco, and 2023 F-250 SD vehicles with TREAD labels stating incorrect load carrying capacity, which could result in vehicle overload and increase crash risk.
Product
FORD — FORD F-250 SD, RANGER, BRONCO
Category
Vehicle
Distribution
Distributed nationwide