State

Illinois product recalls

73,566 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: 2,050
Severe: 3,018
Most recent: 2026-10-24

Of the 11,652 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 3,018 (26%) are Severe.

Which agencies issued them

These figures cover only the 11,652 recalls whose distribution notice names Illinois specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23951–23975 of 85218

HighFDA (Drugs)·D-0768-2022·2022-04-20
Clobetasol Propionate Lotion Recalled Due to Manufacturing Deviations
Preferred Pharmaceuticals is recalling Clobetasol Propionate Lotion 0.05% distributed in Illinois due to manufacturing deviations and discontinued stability study program. Consumers should contact their healthcare provider.
Product
Clobetasol Propionate Lotion 0.05%, Generic for Temovate, 118 mL bottle, Rx Only, Mfg: Teligent Pharma, Inc., PREFERRED Pharmaceuticals, Inc., The Physician's Solution, NDC 68788-7768-01
Category
Drug
Distribution
1 state
HighFDA (Food)·F-0995-2022·2022-04-20
Skippy Reduced Fat Peanut Butter recalled for potential steel contamination
Skippy Reduced Fat Creamy Peanut Butter (40 oz) is being recalled due to potential steel contamination. No illnesses have been reported.
Product
SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz (2 LB 8 OZ) 1.13 kg UPC 037600105200 packaged in clear plastic jar with blue label.; SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz. (2 LB 8 OZ) 1.13 kg UPC 037600105200 packaged in clear plastic jar with blue label and…
Category
Food
Distribution
21 states
HighFDA (Devices)·Z-0922-2022·2022-04-20
FDA Recalls Abbott Vascular Priority Pack Accessory Kits for Leak and Connection Issues
Abbott Vascular is recalling 23 lots of Priority Pack accessory kits and packs due to reports of leaks and loose connections in the devices.
Product
20/30 Priority Pack Accessory Kit/.096 RHV - REF 1000186 WPL2122270-01 (2019-03-01) 20/30 Priority Pack w/.115 RHV - REF 1000186-115 WPL2122270-02 (2019-03-01)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0872-2022·2022-04-20
Conductivity Sensors in Dialog Hemodialysis Systems May Crack and Leak
B Braun Medical Inc is recalling conductivity sensors used in Dialog and Dialog+ hemodialysis systems due to potential cracks that could cause dialysate circuit leaks, affecting ultrafiltration during treatment.
Product
Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems. Conductivity Sensor (BIC) - VERSION 2, Article Code Number 3456102A. These conductivity sensors may be used as spare parts for the following dialysis machines: 710200L (UDI 04046963686345), 710200S (UDI…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0994-2022·2022-04-20
Wilton Cookie Bunny Hutch Kit Recalled for Missing Milk Allergen
Wilton Industries is recalling specific lots of Chocolate Cookie Bunny Hutch Kit because milk is not listed in the allergen statement, despite being present in the product.
Product
Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit, UPC: 0070896117274, total weight 28.7oz
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0940-2022·2022-04-20
CLARAVUE ECG Electrode May Fail to Deliver Effective Defibrillation
CLARAVUE Pre-wired ECG electrodes may not meet electrical safety standards for defibrillation, potentially delivering an ineffective electrical charge during emergency use. This is a Class II recall affecting devices nationwide.
Product
CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0873-2022·2022-04-20
Hemodialysis Conductivity Sensors recalled for potential cracks and dialysate leaks
B Braun Medical Inc is recalling conductivity sensors used in Dialog hemodialysis systems due to potential cracking during use, which could cause leaks in the dialysate circuit and improper ultrafiltration. Affected patients should contact their healthcare provider.
Product
Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems. Conductivity Sensor (END) - VERSION 2, Article Code Number 3456103A. These conductivity sensors may be used as spare parts for the following dialysis machines: 710200L (UDI 04046963686345), 710200S (UDI…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0931-2022·2022-04-20
Siemens Atellica CH Lithium reagent recalled for potential reagent carryover
Siemens Healthcare Diagnostics recalls approximately 2,158 units of Atellica CH Lithium_2 reagent (Lot Numbers 110108, 110185, 110238, 110302) due to potential for reagent carryover affecting quality control results, patient samples, and calibrator results.
Product
Atellica CH Lithium_2 (LITH_2), Siemens Material Number 11097637
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0928-2022·2022-04-20
Siemens Atellica CH Calcium_2 Reagent Carryover Recall
Siemens is recalling Atellica CH Calcium_2 diagnostic reagent due to potential reagent carryover that could impact quality control, patient samples, and calibrator results. The recall affects approximately 2,395 units distributed globally and in the US.
Product
Atellica CH Calcium_2 (CA_2), Siemens Material Number 11097644
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0903-2022·2022-04-20
Access-9 Hemostasis Valves Recalled for Guidewire Entrapment Risk
Merit Medical Systems is recalling 36,445 Access-9 Large Bore Hemostasis Valves due to an internal gap that can trap the guidewire, potentially delaying medical procedures.
Product
Access-9 Large Bore Hemostasis Valves, Catalog Code: 580775001, IN8112/C, K05-00053H, K05-00109G, K05-00137K, K05-00410G, K05-00438G, K05-00502F, K05-00587D, K05-01052, K05-01706C, K05-01880K, K05-02130, K05-02595, K09-12599A, K10-05487P, K12-00264, MAP111/F, MAP112/B, MAP112/F…
Category
Medical Device
Distribution
49 states
HighFDA (Food)·F-0983-2022·2022-04-20
Kroger Buttermilk Pancake & Waffle Mix Recalled for Foreign Material Contamination
Kroger Buttermilk Pancake & Waffle Mix with specific lot codes may contain foreign materials. Consumers who purchased this product should not use it.
Product
Item # 714-0706, Kroger Buttermilk Pancake & Waffle Mix. Product is shelf stable and packaged in a box. net wt. 2 lbs., UPC 0 11110 88219 6.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0934-2022·2022-04-20
Surgical Head Fixation Device Mount Clamp Assembly Deflection Recall
Deerfield Imaging recalls the Trumpf Mount Clamp Assembly component used in surgical head fixation devices. The clamp may deflect during use and become difficult to loosen after procedures, potentially requiring surgical intervention.
Product
Trumpf Mount Clamp Assembly (table adapter component), part #118704-000, a component of the IMRIS HFD100 head fixation device, models #119629-000 and #119630-000, which are used with ORT400 operating room tables.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0910-2022·2022-04-20
Orthopedic Surgical Instrument Kit Recalled for Improper Driver Fit
The Nextra Hammertoe Correction System surgical kit is being recalled due to an oversized driver that cannot properly connect to and remove from the implant. This defect can delay surgery.
Product
Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: NX-4532K Orthopedic surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0985-2022·2022-04-20
Krusteaz Buttermilk Pancake Mix Product Recalled Nationwide for Foreign Materials
Krusteaz Buttermilk Pancake Mix (Lot code KX2066, best-by 3/6/2024) is being recalled nationwide due to foreign materials. Consumers should not consume this product.
Product
Item # 721-0200, Krusteaz Buttermilk Pancake Mix. Product is shelf stable and packaged in a box. net wt. 2 lbs., UPC 0 41449 00110 4.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0990-2022·2022-04-20
Gordon Choice Yellow Cake Mix nationwide recall for foreign materials
Continental Mills is recalling Gordon Choice Yellow Cake Mix (lot KX2066) nationwide due to the presence of foreign materials. The recall was voluntarily initiated on March 10, 2022.
Product
Item # 744-4875, Gordon Choice Yellow Cake Mix. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 93901 24575 5
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0935-2022·2022-04-20
ECG Electrode Set Fails Electrical Safety, May Prevent Effective Defibrillation
Graphic Controls' CLARAVUE pediatric electrode set fails electrical safety standards. The device may not deliver adequate charge during defibrillation, potentially rendering emergency treatment ineffective.
Product
CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776 50401-US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0943-2022·2022-04-20
Ventilator trolley mounting brackets can detach and cause device to fall
The mounting brackets on Breas Ventilator Trolleys can become detached, allowing ventilators to fall. This poses an injury risk to people near the equipment.
Product
Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS ventilator models Article no 007384
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0921-2022·2022-04-20
Abbott Vascular 20/30 Indeflator Recalled for Leaks and Connection Failures
Abbott Vascular recalls 20/30 Indeflator medical devices due to increased complaints of leaks and loose connections. The recall affects 17 product lots distributed nationwide and internationally.
Product
20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0941-2022·2022-04-20
Medline Laryngeal Masks recalled due to potential cuff disconnection
Medline Industries is recalling approximately 8,990 cases of Standard PVC Laryngeal Masks distributed nationwide because the mask cuff may disconnect from the breathing tube.
Product
Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V267000·2022-04-20
Certain BMW Vehicles: Sunroof May Close Without Key Fob Present
BMW is recalling 2019-2023 X5, X6, X7, and 4 Series vehicles because the sunroof may close without the key fob inside, creating injury risk. Dealers will reprogram the control unit free of charge.
Product
BMW — BMW X7, X5, X6, M440I
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0936-2022·2022-04-20
Recalled CLARAVUE Pre-wired Electrode Set May Fail During Defibrillation
Graphic Controls is recalling CLARAVUE Pre-wired Electrode sets because they fail to meet electrical safety specifications for defibrillators, potentially delivering inadequate charge during emergency treatment.
Product
CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600 US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0991-2022·2022-04-20
Fish Breader Recalled Nationwide for Foreign Material Contamination
Continental Mills is recalling Gordon Choice Southern Style Fish Breader (Lot KX2065) nationwide due to the presence of foreign materials. Consumers should not consume this product and should return it to the place of purchase.
Product
Item # 744-4930, Gordon Choice Southern Style Fish Breader. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 93901 75622 0.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0912-2022·2022-04-20
Orthopedic surgical hammertoe instrument recalled for improper component sizing
Nextremity Solutions is recalling the Nextra Hammertoe Correction System due to an oversized driver component that makes it difficult to properly connect and remove during surgery.
Product
Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: NX-3532K Orthopedic surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0987-2022·2022-04-20
IHOP Pancake Mix Recalled Nationwide for Foreign Material Contamination
Continental Mills is recalling 240 cases of IHOP Pancake Mix (Item #743-0278) nationwide due to the presence of foreign materials. Affected lots are KX2062 and KX2063 with a best-by date of 9/1/2022.
Product
Item # 743-0278, IHOP Pancake. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 41449 47540 0.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0900-2022·2022-04-20
FDA Updates Labeling for LIPOSORBER LDL Adsorption Column Due to Anaphylactoid Shock Risk
LIPOSORBER LA-15 LDL Adsorption Column labeling has been updated to address a risk of severe anaphylactoid reactions and shock in patients receiving treatment while taking ACE inhibitors.
Product
LIPOSORBER System, Model: LA-15, consisting of: Apheresis machine, product# 101445 model: MA-03, and disposables (product#, model) [#101447, KP-05 Sulflux Plasma Separator], [#101473, HDE KP-05 Sulflux Plasma Separator], [#101785, LA-15 (AU) LDL Adsorption Column…
Category
Medical Device
Distribution
34 states