The Recall Desk

State

Illinois product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

76–100 of 85236

  • ModerateFDA (Devices)·Z-0188-2027·2026-10-21

    Healthmark Vinyl Instrument Guards Recalled for Labeling Non-Compliance

    Healthmark Industries is recalling 12.8 million vinyl instrument guards because their labeling does not comply with FDA regulations and steam sterilization instructions have been updated.

    Product
    Vinyl Instrument Guards, labeled as: 1) VENTED INSTRUMENT GUARD 1/16 X 3/4H - WHITE, Model Number 09-1-011; 2) WHITE VENTED INSTRUMENT GUARD 1/16 X 3/4, Model Number 09-1-011; 3) VENTED INSTRUMENT GUARD 5/64 X 3/4 - BLUE, Model Number 09-1-012; 4) BLUE VENTED INSTRUMENT GUARD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0178-2027·2026-10-21

    Medline surgical convenience kits recalled for non-conforming cannula components

    Medline is recalling 165 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: OPEN HEART, Medline Product Number/SKU DYNJ902898D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0185-2027·2026-10-21

    Medline Recalls CONMED AirSeal Access Port Kits Due to Overpressure Alerts

    Medline Industries is recalling 3,551 CONMED AirSeal Access Port kits due to potential overpressure alerts and system venting that may delay or end procedures.

    Product
    Convenience Kits containing CONMED AirSeal Access Ports KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0157-2027·2026-10-21

    In2bones Recalls Partially Threaded Bone Screws Due to Labeling Error

    In2bones USA, LLC is recalling 29 bone screws labeled as fully threaded but actually partially threaded due to a labeling error.

    Product
    REF: P65 ST862 CoLag SCREW, FT, 6.7X62.5 mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0184-2027·2026-10-21

    Medline recalls CONMED AirSeal Access Port kits due to pressure alerts

    Medline Industries is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports because they may produce erroneous overpressure alerts and system venting.

    Product
    Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0190-2027·2026-10-21

    Radiometer ABL90 FLEX Analyzers Recalled for Inaccurate Results

    Radiometer Medical ApS is recalling ABL90 FLEX and ABL90 FLEX PLUS analyzers due to a risk of potentially inaccurate results requiring updated instructions for use.

    Product
    The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point-of-care setting. These tests are only performed under a physician's order.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0162-2027·2026-10-21

    Magellan LeadCare II Blood Lead Test Kit Recall for Labeling Error

    Magellan Diagnostics is recalling 321 LeadCare II Blood Lead Test Kits due to a potential expiration date labeling error that may delay test results.

    Product
    LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V687000·2026-10-20

    Lexus NX Vehicles Recalled for Instrument Panel Display Failure

    Toyota is recalling 2022-2024 Lexus NX vehicles because the instrument panel may fail to display critical warnings, increasing crash risk.

    Product
    LEXUS — LEXUS NX PLUG-IN HYBRID, NX HYBRID, NX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V688000·2026-10-20

    Ford Recalls Lincoln Hybrid Vehicles for Transmission Defect

    Ford is recalling 2026-2027 Lincoln Nautilus and 2027 Corsair Hybrids because corrosion may cause the vehicle to unexpectedly shift into neutral while driving.

    Product
    LINCOLN — LINCOLN NAUTILUS HYBRID, CORSAIR HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E073000·2026-10-20

    Ford Recalls ABS Modules With Incorrect Software Programming

    Ford is recalling certain Anti-Lock Brake System (ABS) modules that may have incorrect software, potentially degrading brake balance and increasing stopping distance.

    Product
    SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V689000·2026-10-20

    Ford Recalls F-Series Trucks Due to Tailgate Cable Failure Risk

    Ford is recalling certain 2026-2027 F-Series trucks because a tailgate cable may fail under heavy loads, posing an injury risk.

    Product
    FORD — FORD F-250 SD, F-350 SD, F-150, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E074000·2026-10-20

    Great Dane Trailer Landing Gear Recall Due to Weld Failure Risk

    Great Dane Trailers is recalling specific landing gear assemblies because k-brace welds may fail, causing the gear to collapse and increasing injury risk.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER:HOSES/CABLES/RODS/GEARS/STRUT/CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V686000·2026-10-20

    Forest River Recalls 2023-2026 Pause Travel Trailers for Wiring Defect

    Forest River is recalling 2023-2026 Pause travel trailers because an incorrect connector was used for 12-volt solar panel wires, which may increase the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER PAUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V685000·2026-10-19

    Subaru Recalls 2026 Forester and Crosstrek for Ball Joint Defect

    Subaru is recalling 2026 Forester and Crosstrek vehicles because a loose ball joint may separate, causing loss of control. Owners should not drive until repaired.

    Product
    SUBARU — 2026 SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·026-2026·2026-10-17

    Kayem Foods Recalls Ready-to-Eat Meat and Poultry Due to Temperature Abuse

    Kayem Foods Inc. is recalling approximately 1.6 million pounds of ready-to-eat meat and poultry products because they may have experienced temperature abuse during storage.

    Product
    Kayem Foods Inc. — Kayem Foods Inc. Recalls Meat and Poultry Products Due to Possible Temperature Abuse
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V680000·2026-10-16

    Alliance RV Recalls Valor and Delta Trailers Due to Fire Risk

    Alliance RV is recalling 2025-2027 Valor and 2026-2027 Delta recreational trailers because a power cord fuse may not provide adequate circuit protection, increasing fire risk.

    Product
    ALLIANCE RV — ALLIANCE RV DELTA, VALOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V681000·2026-10-16

    Forest River Recalls 2026-2027 Cedar Creek Trailers for Fire Risk

    Forest River is recalling 2026-2027 Cedar Creek recreational trailers because a slide switch may lack proper overcurrent protection, creating a fire risk.

    Product
    FOREST RIVER — FOREST RIVER CEDAR CREEK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V682000·2026-10-16

    Porsche Recalls 2024 Models for Center Lock Wheel Bolt Fracture Risk

    Porsche is recalling 548 specific 2024 models because a center lock wheel bolt may fracture, causing the wheel to detach and increasing crash risk.

    Product
    PORSCHE — PORSCHE 718 SPYDER RS, 911 CARRERA GTS, 911 GT3, 911 GT3 RS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·27024·2026-10-15

    3M Recalls Scotch Thermal Laminators Due to Fire Hazard

    3M is recalling Scotch thermal laminators because they can overheat and catch fire. Consumers should stop using the devices and contact 3M for a refund.

    Product
    Scotch™ Thermal Laminators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27025·2026-10-15

    HatsanUSA Recalls Blitz Air Rifles Due to Projectile Hazard

    HatsanUSA is recalling Blitz and Blitz 777 air rifles because they can fire unexpectedly, posing a risk of serious injury or death.

    Product
    Blitz and Blitz 777 air rifles
    Category
    Consumer Product
    Distribution
    Distributed nationwide