The Recall Desk

State

Illinois product recalls

72,936 recalls have nationwide distribution and so reach Illinois. 11,603 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total
11,603
Critical
2,039
Severe
2,516
Most recent
2026-09-09

Of the 11,603 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 2,516 (22%) are Severe.

These figures cover only the 11,603 recalls whose distribution notice names Illinois specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2876–2900 of 84539

  • HighCPSC·26346·2026-03-26

    CCCEI power strips lack supplementary overcurrent protection posing fire risk

    CCCEI power strips are being recalled because they do not contain supplementary overcurrent protection, creating a fire risk if overloaded. Two reports of sparking and melting have been received.

    Product
    CCCEI Power Strips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26350·2026-03-26

    MPINOI adult portable bed rails pose entrapment and asphyxiation hazard

    MPINOI adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and mattress, and the rails lack the required hazard warning labels.

    Product
    MPINOI Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26342·2026-03-26

    AirClub convertible bassinets create an opening between sleeper and mattress

    AirClub convertible bassinets are being recalled because the mechanism used to attach the product to an adult bed creates an opening between the bedside sleeper and the mattress, posing a fall hazard to infants.

    Product
    AirClub Convertible Bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V191000·2026-03-26

    ABC Bus Recalls Van Hool Buses Due to Incorrect Window Glazing

    ABC Bus is recalling specific Van Hool bus models because the front entrance door window may have incorrect glazing, which could reduce driver visibility and increase crash risk.

    Product
    VAN HOOL — VAN HOOL CX45, TX45, C2045, T2145
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V189000·2026-03-26

    Chrysler Voyager and Pacifica side curtain airbags recall

    Chrysler is recalling certain 2022–2026 Voyager and Pacifica vehicles because the right and left side curtain airbags may have insufficient pressure retention due to improperly sealed seams, increasing the risk of ejection and injury during a crash.

    Product
    CHRYSLER — CHRYSLER PACIFICA, VOYAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26345·2026-03-26

    GLMZZ fidget magnet balls are high-powered magnets posing ingestion hazard

    GLMZZ Fidget Magnet Ball Toy Sets are being recalled because they are high-powered magnets, violating the mandatory standard for toys and posing an ingestion hazard to children.

    Product
    GLMZZ Fidget Magnet Ball Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26344·2026-03-26

    Sunnyyes LED mini lights let children access lithium coin batteries

    Sunnyyes LED mini lights are being recalled because the lithium coin batteries can be easily accessed by children, the remote battery compartment screw does not stay attached, and the packaging lacks required warnings.

    Product
    Sunnyyes LED Mini Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0572-2026·2026-03-25

    Butter-Rich Powder Recalled Due to Potential Salmonella Contamination

    Bluegrass Ingredients Inc. is recalling Butter-Rich Powder (50 LB. bags) due to potential Salmonella contamination. The product was distributed to Florida, Illinois, and Maryland.

    Product
    Butter-Rich Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·H-0573-2026·2026-03-25

    Butter Powder Recalled Due to Positive Salmonella Contamination

    Bluegrass Ingredients Inc. is recalling Butter Powder (50 LB bags, Product Number BDF0006, Lot 6018) due to positive Salmonella contamination. The product was distributed to Florida, Illinois, and Maryland.

    Product
    Butter Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0528-2026·2026-03-25

    Webcol alcohol prep pads recalled as Class I for microbial contamination

    Cardinal Health is recalling Webcol Alcohol Prep pads because of non-sterility, with microbial contamination identified as Paenibacillus phoenicis. The FDA has classified this recall as Class I.

    Product
    Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive, Waukegan, IL 60085.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V186000·2026-03-25

    2025-2026 Volvo VNL Trucks Delayed Service Brake Release Recall

    Volvo Trucks is recalling certain 2025-2026 VNL (4) vehicles because the service brake may take longer than expected to release, creating a crash risk and violating Federal Motor Vehicle Safety Standard 121.

    Product
    VOLVO — VOLVO VNL (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0581-2026·2026-03-25

    Great Value Fat Free Cottage Cheese Recalled for Potential Under-Pasteurization

    Saputo Cheese USA is recalling Great Value Fat Free Cottage Cheese Small Curd due to potential under-pasteurization caused by a broken seal on the pasteurizer. The product was distributed to multiple states.

    Product
    Great Value Fat Free Cottage Cheese Small Curd 0% Milkfat NET WT 24OZ UPC 0 78742 37339 3 DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·H-0583-2026·2026-03-25

    Great Value Cottage Cheese Small Curd Recall Due to Potential Underpasteurization

    Saputo Cheese USA is recalling Great Value Cottage Cheese products because a broken pasteurizer seal may have resulted in underpasteurized product. The recall affects 16oz, 24oz, and 3lb containers distributed to multiple states.

    Product
    Great Value Cottage Cheese Small Curd 4% Milkfat NET WT 16oZ UPC 0 78742 37235 8; 24oz UPC 0 78742 37236 5 & 3lb UPC 0 78742 14797 0 DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1569-2026·2026-03-25

    GE Centricity Viewer 7.0 may expose login credentials on workstations

    GE Medical Systems is recalling Centricity Universal Viewer software versions 7.0 through 7.0 SP2.0.1 because user login credentials may be exposed on the local client workstation.

    Product
    Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 5826659-027, 5826659-029, 5826659-032, 5826659-033, 5826659-028, 5826659-034, 5826659-030, 5826
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1586-2026·2026-03-25

    Hologic Aptima HPV assay may produce invalid or false negative results

    Hologic is recalling one master lot of the Aptima HPV Assay because the product exhibits potential to generate either invalid or false negative results.

    Product
    Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima HPV assay Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0398-2026·2026-03-25

    Dexamethasone injection failed impurity specifications at product expiry testing

    Somerset Therapeutics is recalling one lot of Dexamethasone Sodium Phosphate Injection after out-of-specification impurity results at product expiry during long term stability testing.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1582-2026·2026-03-25

    ConvaTec EsteemBody drainable pouch REF 423643 may leak

    ConvaTec is recalling two lots of the EsteemBody Drainable Pouch, REF 423643, because the drainable large pouch may leak due to a manufacturing issue.

    Product
    Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0582-2026·2026-03-25

    Great Value Lowfat Cottage Cheese Recalled for Possible Under-Pasteurization

    Saputo Cheese USA is recalling Great Value Lowfat Cottage Cheese due to potential under-pasteurization caused by a broken pasteurizer seal. The product was distributed to ten states.

    Product
    Great Value Lowfat Cottage Cheese Small Curd 2% Milkfat NET WT 24OZ UPC 0 78742 11673 0 DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1570-2026·2026-03-25

    GE Centricity Viewer 6.0 may expose login credentials on workstations

    GE Medical Systems is recalling Centricity Universal Viewer software versions 6.0 through 6.0 SP10.4.1 because user login credentials may be exposed on the local client workstation.

    Product
    Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 210
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1573-2026·2026-03-25

    Welch Allyn vision screener display may flicker inducing photosensitive seizures

    Baxter is recalling the Welch Allyn Spot Vision Screener VS100 on software version 3.2.0.1 because the display screen may unintentionally flicker, which may induce photosensitive seizure activity.

    Product
    Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic One unit pe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1571-2026·2026-03-25

    GE Centricity Viewer 5.0 may expose login credentials on workstations

    GE Medical Systems is recalling Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 because user login credentials may be exposed on the local client workstation.

    Product
    Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-026, 2088026-115, 2088026-043, K2042VJED, 2088026-132, 2088026-003, 2088026-110, 2
    Category
    Medical Device
    Distribution
    Distributed nationwide