The Recall Desk

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.

19576–19600 of 85036

  • HighFDA (Drugs)·D-0262-2023·2023-02-08

    Diltiazem Hydrochloride extended-release capsules recalled due to failed quality specifications

    Sun Pharmaceutical is recalling Diltiazem Hydrochloride Extended-Release Capsules (360 mg) due to failed impurity specifications and dissolution testing found during FDA laboratory evaluation. The recall affects five lot numbers distributed nationwide.

    Product
    DILTIAZEM HYDROCHLORIDE — DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1022-2023·2023-02-08

    SynCardia Total Artificial Heart System Recalled for Cannula Tears

    SynCardia Systems is recalling its Total Artificial Heart System due to reported tears in the cannula caused by wear and tear stress. Approximately 1,732 systems worldwide are affected.

    Product
    SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1038-2023·2023-02-08

    Turbett Surgical Container TS1000 may have weld failures breaching sterile barrier

    Turbett Surgical Container TS1000 may have weld failures that breach the sterile barrier, potentially resulting in unsterile instruments being used in medical procedures and risking patient infection or injury.

    Product
    Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1047-2023·2023-02-08

    Medline UNITE Foot & Ankle Drill Bit Recalled for Intra-operative Screw Failure Risk

    Medline Industries recalls 190 UNITE foot and ankle drill bits due to observed screw failure during surgery. When used to pre-drill holes for certain screw sizes, the drill bits may fail under surgical torque, creating risk during procedures.

    Product
    MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1030-2023·2023-02-08

    Non-sterile procedural trays risk sterile packaging breach

    Medline Industries is recalling non-sterile laparoscopic procedural trays containing sterile blades that may puncture the outer packaging, potentially breaching the sterile barrier. 260 cases have been distributed nationwide.

    Product
    Non-sterile procedural trays labeled as LAPAROSCOPIC, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1029-2023·2023-02-08

    MEDLINE procedural trays recalled for potential sterile packaging breach

    MEDLINE is recalling procedural trays because sterile blades within the kits could puncture the outer foil packaging, potentially breaching the sterile barrier.

    Product
    Non-sterile procedural trays labeled as CRANI, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·23115·2023-02-08

    Fabuloso Multi-Purpose Cleaners Recalled for Bacterial Contamination Risk

    Colgate-Palmolive is recalling about 4.9 million Fabuloso Multi-Purpose Cleaners due to contamination with Pseudomonas bacteria. People with weakened immune systems, external medical devices, or underlying lung conditions face a risk of serious infection from exposure.

    Product
    Fabuloso Multi-Purpose Cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1027-2023·2023-02-08

    Temperature Monitoring Adapter Detachment in Cardiopulmonary Bypass Oxygenators

    Medtronic is recalling cardiopulmonary bypass equipment because the Temperature Monitoring Adapter can come loose during setup or disassembly, potentially compromising temperature monitoring during heart surgery.

    Product
    Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, REF BB811. Used in Cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0323-2023·2023-02-08

    Vitamin B Complex dietary supplement recalled due to undeclared niacin

    Professional Complementary Health Formulas, LLC recalls Vitamin B Complex dietary supplement (lot 1092715) due to undeclared niacin affecting 299 bottles distributed nationwide.

    Product
    Vitamin B Complex packaged in white plastic bottle labeled in part, "***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Vitamin B Complex DIETARY SUPPLEMENT 60 Capsules***Supplement Facts Serving Size: One Capsule***Vitamin B1 (as thiamine Hcl) 80mg 6667% Vitamin B2 (as riboflavin)…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0322-2023·2023-02-08

    Inositol dietary supplement recalled due to undeclared niacin

    Professional Complementary Health Formulas is recalling Inositol dietary supplement (Lot 1032526, UPC 4065111562) distributed in NY, OR, PA, UT, WI, and WY due to undeclared niacin. Consumers should stop using the product.

    Product
    Inositol packaged in white plastic bottle with UPC 4065111562 and labeled in part, "***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Inositol DIETARY SUPPLEMENT 360 Capsules***Supplement Facts Serving Size: One Capsule***Inositol 920 mg***Other Ingredients: Vegetarian capsule…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1049-2023·2023-02-08

    Lucid TCD 2.0 Transcranial Ultrasound System Recalled for Hard Drive Failure

    The Lucid TCD 2.0 System has a faulty hard drive that causes the device to freeze and reboot. Eventually, the system becomes completely inoperable.

    Product
    Lucid TCD 2.0 System, Model: NA-LUCM1. Transcranial Ultrasound System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1050-2023·2023-02-08

    Ultrasound system hard drive defect causes device freezing and failure

    FDA recall of NovaGuide Intelligent Ultrasound System due to faulty hard drive causing device freezing and eventual system failure.

    Product
    NovaGuide Intelligent Ultrasound System, Model: NA-RBTSYS1. Comprised of NovaBot Automated Headset (AKA: NeuralBot, Model: NA-RBT1) and Lucid TCD 2.0 Transcranial Doppler Ultrasound (Model: NA-LUCM1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1041-2023·2023-02-08

    Biopsy marker device recalled for label and contents mismatch

    Carbon Medical Technologies recalls 550 Mammotome MammoStar biopsy markers due to a labeling error. The label identifies one product but the package contains a different marker size and shape.

    Product
    Mammotome MammoStar Biopsy Site Identified, REF STAR1401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V056000·2023-02-07

    Pleasant Valley Teardrop Trailers Recalled for Gas Leak Risk

    Pleasant Valley is recalling 2023 Teardrop TAB 320s and TAB 320CSS travel trailers because internal aluminum burner tubes may fracture, causing a gas leak that could lead to fire.

    Product
    PLEASANT VALLEY — PLEASANT VALLEY TEARDROP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V057000·2023-02-07

    Maintainer Service Trucks Recalled for Uncontrolled Crane Movement Risk

    Maintainer is recalling 2019-2023 service trucks with hydraulic cranes because power loss may cause uncontrolled movement, increasing injury risk.

    Product
    MAINTAINER — MAINTAINER CRANE W/ SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E008000·2023-02-07

    Lippert Recalls RV Entry Door Latches Due to Failure Risk

    Lippert is recalling specific RV entry door latches that may fail, preventing entry or exit. This defect increases the risk of injury during an emergency.

    Product
    LATCHES/LOCKS/LINKAGES:DOORS:LATCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V054000·2023-02-06

    Nova Bus Recalls 2022 LFS Transit Buses for Steering Hose Defect

    Nova Bus is recalling 2022 LFS transit buses because the power steering hose may not have been assembled correctly, which can result in hose detachment and a loss of power steering assist.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E007000·2023-02-06

    Tokai Rika Seat Belt Assemblies Recalled for Force-Limiter Defect

    Tokai Rika is recalling certain front-seat outer right-side seat belt assemblies because the force-limiter may not operate correctly. This defect could allow the belt to extend further than intended, increasing injury risk in a crash.

    Product
    SEAT BELTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V053000·2023-02-05

    2022 Can-Am Spyder F3 Recalled for Rearview Mirror Lens Detachment

    Bombardier is recalling 2022 Can-Am Spyder F3 and F3-S motorcycles because the rearview mirror lens may detach, reducing rear visibility and increasing crash risk.

    Product
    CAN-AM — CAN-AM SPYDER F3-S, SPYDER F3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V052000·2023-02-04

    Nexus RVs Recalls 2022 Motorhomes Due to Awning Seam Separation Risk

    Nexus RVs is recalling 2022 motorhomes because a welded seam on the electric retractable awning may separate, potentially allowing the awning to drop and increase the risk of injury.

    Product
    NEXUS — NEXUS GHOST, WRAITH, VERRADO, REBEL 4X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·004-2023·2023-02-03

    USDA Recalls Ineligible Frozen Catfish Imported from India

    Delight Foods USA LLC and Delight Foods LLC are recalling approximately 2,961 pounds of frozen catfish imported from India because the country is ineligible to export these products to the U.S.

    Product
    Delight Foods USA LLC Recalls Ineligible Frozen Siluriformes Products Imported from India
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V050000·2023-02-03

    BMW Recalls 2023 760i and i7 Models Due to Airbag Software Defect

    BMW is recalling 397 vehicles because a software error may disable front passenger airbags and active headrests, increasing injury risk in crashes.

    Product
    BMW — BMW 760I, I7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V051000·2023-02-03

    BMW S 1000 XR and R motorcycles recall for deactivated safety feature

    BMW is recalling 2020-2023 S 1000XR and 2022-2023 S 1000R motorcycles because a software update may have deactivated the front wheel lift-off assistant feature without notifying riders, increasing the risk of unexpected handling and loss of control.

    Product
    BMW — BMW S 1000 XR, S 1000 R
    Category
    Vehicle
    Distribution
    Distributed nationwide