The Recall Desk

State

Illinois product recalls

72,992 recalls have nationwide distribution and so reach Illinois. 11,607 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total
11,607
Critical
2,039
Severe
2,517
Most recent
2026-09-25

Of the 11,607 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 2,517 (22%) are Severe.

These figures cover only the 11,607 recalls whose distribution notice names Illinois specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8301–8325 of 84599

  • HighFDA (Drugs)·D-0228-2025·2025-02-26

    Lorazepam tablets recalled due to failed potency and impurity specifications

    The Harvard Drug Group LLC is recalling Lorazepam 2mg tablets due to out-of-specification results in potency and impurity testing. Affected products were distributed nationwide.

    Product
    LORAZEPAM — LORAZEPAM (LORAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1203-2025·2025-02-26

    Dexcom G6 glucose receiver may fail to deliver high or low alarms

    Under rare conditions, the Dexcom G6 receiver may fail to send high or low glucose alarms due to a software error, potentially delaying detection of dangerous blood sugar levels.

    Product
    Dexcom G6, Continuous Glucose Monitoring System, REF: STK-OR-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1174-2025·2025-02-26

    DeRoyal AMG Suction Connector Tubing connection may fail to seal

    DeRoyal Industries is recalling AMG Suction Connector Tubing because the connection between the tubing and suction device may not seal properly, potentially affecting patient care.

    Product
    DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid movement
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-1190-2025·2025-02-26

    RayStation radiation therapy software: incorrect density uncertainty calculations in dose planning

    RayStation radiation therapy planning software versions 4.5 through 2024B contains an inconsistency in density uncertainty calculations affecting proton and light ion dose computations. No illnesses reported.

    Product
    Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 12.0.0.932, 12.1.0.1221, 12.0.3.68, 12.0.4.12 and 12.3.0.119 Software Version: RayStation 11B and 11B Service Pack 1, 2, 3 and Service Pack Toshiba 1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1175-2025·2025-02-26

    3M Prevena Plus Negative Pressure Therapy System Recalled for Leak Alarm Malfunctions

    KCI USA is recalling 3M Prevena Plus wound therapy systems due to complaints about malfunctioning leak alarms. The recall affects 135,268 units distributed worldwide.

    Product
    3M Prevena Plus 125 Therapy Unit and System Kits REF: PRE3021US Prevena Plus Duo Peel and Place 20cm System Kit, US PRE3201US Prevena Plus Peel and Place 35 cm system Kit, US PRE3201 Prevena Plus Peel and Place 35 cm system Kit PRE4000US Prevena Plus 125 Therapy Unit, U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1195-2025·2025-02-26

    RayStation Radiation Therapy Software Recalled for Dose Calculation Inconsistency

    RayStation radiation therapy planning software is being recalled due to inconsistent handling of density uncertainty in dose calculations for proton and light ion treatment plans. The software defect may affect the accuracy of calculated radiation doses.

    Product
    Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 4.5.1.14, 4.7.2.5, 4.7.3.13, 4.7.4.4, 4.7.5.4 and 4.7.6.7 Software Version: RayStation 4.5.1, 4.7.2, 4.7.3, 4.7.4, 4.7.5 and 4.7.6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0238-2025·2025-02-26

    Atomoxetine Capsules Recalled for Chemical Impurity Above FDA Limits

    Glenmark Pharmaceuticals is recalling 120,000 bottles of Atomoxetine 10 mg capsules nationwide due to N-nitroso Atomoxetine impurity exceeding FDA recommended limits. Multiple lot numbers are affected with expiration dates through July 2026.

    Product
    ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·007-2025·2025-02-25

    L&V Food Supply Recalls Ineligible Frozen Dried Catfish Products

    L&V Food Supply is recalling approximately 1,152 pounds of peppered dried catfish imported from Vietnam because the source establishment is not eligible to export to the U.S.

    Product
    C&T Produce Wholesale Inc. Dba L&v Food Supply Recalls Ineligible Frozen, Dried Silurifomes Products Imported From Vietnam
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·25V115000·2025-02-24

    Kia EV9 rear drive unit motor shaft may be improperly welded

    Kia is recalling certain 2025 EV9 vehicles because the rear gear drive unit motor shaft may have been improperly welded and become damaged, causing a loss of drive power.

    Product
    KIA — KIA EV9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V116000·2025-02-24

    Mercedes-Benz Recalls S-Class Vehicles Due to Front Brake Hose Rupture Risk

    Mercedes-Benz is recalling 2021-2023 S-Class and Maybach vehicles because front brake hoses may rupture and leak fluid, increasing stopping distance and crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S 500, S 580, S 580 E, S 680
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E013000·2025-02-24

    Joyson Recalls Side Curtain Air Bag Inflator Due to Detachment Risk

    Joyson is recalling one side curtain air bag inflator because the ignition holder may detach during deployment, creating a projectile hazard.

    Product
    AIR BAGS:SIDE/WINDOW:CURTAIN:INFLATOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V117000·2025-02-24

    Textron Recalls Cushman and E-Z-GO LSVs for Defective Reflectors

    Textron is recalling 2024-2025 Cushman and E-Z-GO low-speed vehicles because side and rear reflectors do not meet federal safety standards, increasing crash risk.

    Product
    CUSHMAN — CUSHMAN, E-Z-GO HAULER PRO LSV, LIBERTY LSV, TOUR LSV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·006-2025·2025-02-23

    LPK1 Recalls Chicken Caesar Wraps Due to Undeclared Fish Allergen

    LPK1 is recalling ready-to-eat chicken Caesar wraps because the included dressing contains undeclared fish (anchovies). No adverse reactions have been reported.

    Product
    Fresh & Ready Foods LLC — LPK1 Recalls Ready-to-Eat Chicken Caesar Wrap Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V109000·2025-02-21

    BMW X3 battery cable connection can overheat stalling the engine

    BMW is recalling certain 2025 X3 30 xDrive vehicles because the connection between the positive battery cable and the starter-generator may be improperly tightened and overheat.

    Product
    BMW — BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V114000·2025-02-21

    Spartan RV chassis fuel filter hose can separate causing leak and stall

    Shyft Group is recalling certain 2022-2025 Spartan RV Chassis K2 vehicles with Cummins L9 diesel engines because the remote fuel filter hose may separate from the fitting.

    Product
    SPARTAN — SPARTAN K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V111000·2025-02-21

    Forest River trailer weight rating placard may exceed safety chain rating

    Forest River is recalling certain 2017-2025 Coachmen Catalina, 2020-2025 Aurora and 2025 Puma travel trailers because the Gross Vehicle Weight Rating on the Federal placard may exceed the safety chain rating.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN AURORA, CATALINA, PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25150·2025-02-20

    SuperATV Carrier Bearings for Polaris RZR Recalled for Fire and Burn Hazards

    SuperATV carrier bearings for Polaris RZR XP Turbo or Turbo S vehicles can allow the drive shaft to contact the fuel tank, causing fuel leaks and fire hazards. SuperATV is offering free replacement bearings to affected consumers.

    Product
    SuperATV carrier bearings for Polaris RZR XP Turbo or Turbo S Recreational Off Highway Vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25138·2025-02-20

    Swagtron SG-5 Boost Electric Scooters Recalled for Fire and Burn Hazards

    Walmart recalls about 17,970 Swagtron SG-5 Boost electric scooters due to lithium-ion batteries that can overheat, smoke, and ignite, causing fire and burn hazards. One incident caused a burn injury and property damage to a residential building.

    Product
    Swagtron SG-5 Swagger 5 Boost Commuter Electric Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide