The Recall Desk

State

Illinois product recalls

20,371 recalls have nationwide distribution and so reach Illinois. 0 additional recalls listed Illinois specifically in their distribution scope.

About recalls in Illinois

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Illinois consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

16151–16175 of 20371

  • HighFDA (Devices)·Z-1480-2022·2022-08-03

    Medtronic Cobalt Implantable Cardioverter Defibrillators Recalled for Cathode Component Defect

    Medtronic is recalling three Cobalt Implantable Cardioverter Defibrillators (CRT-D) due to a manufacturing error that may have resulted in a cathode component being out of specification. Affected patients should contact their physician.

    Product
    Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1470-2022·2022-08-03

    Medline Medical Convenience Kits Recalled for Leaking Isopropyl Alcohol Bottles

    Medline is recalling medical convenience kits distributed nationwide that contain leaking bottles of isopropyl alcohol. Users should stop using the affected kits.

    Product
    Medline Convenience kits labeled as follows: a. BEDSIDE PICC CDS, Model Number CDS984642, b. VASCULAR CDS, Model Number DYNJ902880J, c. VASCULAR CDS, Model Number DYNJ902880K, d. OPEN HEART A & B, Model Number DYNJ904831F, e. OPEN HEART MHS, Model Number DYNJ905394A, f. OPEN HEA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1468-2022·2022-08-03

    HammerTube 2.75mm Implant Recalled for Missing Titanium Plasma Coating

    Paragon 28 recalls HammerTube implants missing their titanium plasma coating. Affected implants were distributed to facilities in Alabama, California, Georgia, Illinois, and Kentucky.

    Product
    HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1289-2022·2022-08-03

    Prescription testosterone gel recalled due to out-of-specification potency

    Teva Pharmaceuticals is recalling testosterone gel lot 1403180 after stability testing revealed out-of-specification assay results indicating superpotency. The affected 12,354 cartons were distributed nationwide.

    Product
    TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1462-2022·2022-08-03

    Medical imaging software may flip left-right brain image orientation

    NordicBrainEX software versions 2.21-2.3.10 may export brain imaging with reversed left-right orientation in certain analysis scenarios, potentially causing diagnostic misinterpretation.

    Product
    nordicBrainEX, software versions 2.21 through 2.3.10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1478-2022·2022-08-03

    Stryker Craniotomy Router May Break and Leave Metal Fragments

    Stryker 2.3mm Tapered Router (craniotomy instrument) may break due to undersized core, leaving metal fragments in the surgical site. This risks damage to critical brain structures or need for additional surgery.

    Product
    Stryker 2.3mm Tapered Router, Catalog no. 5820-071-023 instrument used in craniotomy procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1457-2022·2022-08-03

    X-Stream Irrigation System recalled due to potential fire hazard

    Davol, Inc. is recalling the X-Stream Irrigation System due to a potential fire hazard. The device may cause a fire during use, creating a safety risk.

    Product
    X-Stream Irrigation System (Catalog No. 5551000) and X-Stream Irrigation System Refurbished (Catalog No. 9551000)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1460-2022·2022-08-03

    Da Vinci Surgical Clip Appliers Recalled for Potential Unexpected Motion

    Intuitive Surgical is recalling three models of Da Vinci clip appliers due to potential unexpected motion from partial instrument disengagement. Approximately 90,628 units have been distributed worldwide.

    Product
    Da Vinci X/Xi Large Clip Applier, Model 470230 Da Vinci X/Xi Medium-Large Clip Applier, Model 470327 Da Vinci X/Xi Small Clip Applier, Model 47401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V135000·2022-08-03

    2022 Forest River Cardinal travel trailers recalled for electrical fire risk

    Forest River is recalling certain 2022 Cardinal and related travel trailers due to a loose wire cord at the 50AMP shore power inlet that may cause an electrical short and fire.

    Product
    FOREST RIVER — 2022 FOREST RIVER CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1479-2022·2022-08-03

    Revogene diagnostic test instrument recalled for burn risk from cooling failure

    Meridian Bioscience recalled 459 Revogene diagnostic instruments due to a cooling protection failure that may expose users to heated components, risking minor burn injuries.

    Product
    Revogene, Catalog no. 610210. IVD test instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1291-2022·2022-08-03

    FDA Recalls Divalproex Sodium Tablets for Failed Dissolution Specifications

    Sun Pharmaceutical recalls Divalproex Sodium delayed-release tablets due to failed dissolution specifications discovered during stability testing. The tablets may not dissolve as intended.

    Product
    DIVALPROEX SODIUM — DIVALPROEX SODIUM (DIVALPROEX SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1472-2022·2022-08-03

    Medline Medical Kits Recalled for Leaking Isopropyl Alcohol

    Medline convenience kits containing leaking bottles of isopropyl alcohol are being recalled. Approximately 477 units were distributed nationwide and should not be used.

    Product
    Medline convenience kits labeled as: a. MIDDLE EAR PACK-LF, Model DYNJ0689093V, b. EENT PACK, Model Number DYNJ62927 Model/Catalog Number: a. DYNJ0689093V, b. DYNJ62927
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1477-2022·2022-08-03

    Medical Device Kits Recalled for Leaking Isopropyl Alcohol

    Medline Industries is recalling medical device kits nationwide due to leaking isopropyl alcohol bottles. Approximately 28,745 units are affected. Consumers should stop using affected kits and contact the manufacturer.

    Product
    Z-1477-2022
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1475-2022·2022-08-03

    Medline skin prep kits recalled due to leaking isopropyl alcohol bottles

    Medline Industries is recalling 1,880 units of skin prep convenience kits with models DYNDP1127A and DYNDP1131 distributed nationwide due to leaking bottles of isopropyl alcohol.

    Product
    Medline Convenience kits labeled as: a. WET SKIN PREP TRAY, b. SKIN PREP TRAY W/CHG Model/Catalog Number: Model numbers: a. DYNDP1127A, b. DYNDP1131
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1465-2022·2022-08-03

    ZEISS Axio Observer 5 Microscope Recalled for Incorrect Device Identification Label

    Zeiss is recalling ZEISS Axio Observer 5 microscopes due to an incorrect Unique Device Identification (UDI) label installed on some units. The labeling discrepancy affects device tracking and identification.

    Product
    ZEISS Axio Observer 5 microscope, Product material no. 431006-9901-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V068000·2022-08-02

    Tiffin motorhomes have improperly secured buss bars increasing fire risk

    Tiffin is recalling 2018-2022 Allegro and Allegro Breeze motorhomes where an improperly secured electrical buss bar can cause the DC Distribution Panel to overheat and potentially start fires. Dealers will replace the buss bar with a cable for free.

    Product
    TIFFIN — 2018 TIFFIN ALLEGRO BREEZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V067000·2022-08-02

    Travel Trailer Propane Regulator Failure Fire Risk Recall 2019-2021

    Holiday House is recalling certain 2019-2021 travel trailers with defective propane regulators that may fail and increase propane pressure, enlarging gas appliance flames and creating a fire risk. Dealers will replace the regulator free of charge.

    Product
    HOLIDAY HOUSE — 2019 HOLIDAY HOUSE 24TB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V018000·2022-08-01

    2021 Western Star and Freightliner trucks recalled for brake caliper mounting defect

    Commercial trucks from multiple manufacturers may have incorrectly tightened brake caliper mounting bolts, reducing braking effectiveness. Daimler Trucks North America will notify owners for free inspection and repair.

    Product
    WESTERN STAR — 2021 WESTERN STAR 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V015000·2022-08-01

    [pending] 2021 KEYSTONE CROSSROADS REDWOOD

    Pending LLM rewrite. Source: NHTSA 21V015000.

    Product
    KEYSTONE — 2021 KEYSTONE CROSSROADS REDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22193·2022-07-28

    Evaporator Coil Drain Pans Recall for Fire Hazard Risk

    Daikin Comfort Technologies is recalling about 298,300 evaporator coil drain pans that can overheat, melt, and deform, creating a fire hazard. The company has received 26 fire reports, with no injuries reported.

    Product
    Evaporator coil drain pans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22763·2022-07-28

    Arctic Cat Alterra 600 and Tracker 600 ATVs Recalled for Crash Hazard

    Textron Specialized Vehicles is recalling about 1,750 Arctic Cat Alterra 600 and Tracker 600 ATVs because a fuse in the electrical system can fail during operation, causing sudden loss of engine power and headlights, which poses a crash hazard.

    Product
    Arctic Cat Alterra 600 and Tracker 600 All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22191·2022-07-28

    Ocean Technology Systems Recalls Underwater Communication Devices for Fire Hazard

    Ocean Technology Systems is recalling about 500 underwater communication devices (PowerCom and MilCom models) with RBLi-4 lithium battery packs because water can leak into the battery pack and cause the circuit board to short and ignite after diving, posing a fire hazard.

    Product
    Underwater Communication Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22762·2022-07-28

    KTM, Husqvarna, and GASGAS Competition Motorcycles Recalled for Crash Hazard

    KTM, Husqvarna, and GASGAS are recalling about 3,310 closed course competition motorcycles because the connecting rod can break, posing crash and injury hazards. Owners should stop riding and contact an authorized dealer for a free repair.

    Product
    Closed Course Competition Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22192·2022-07-28

    Kidoozie Play Tents and Playhouses Recalled for Flammability Risk

    Epoch Everlasting Play is recalling about 251,600 Kidoozie play tents and playhouses because the fabric fails to meet flammability standards, posing a burn hazard to children.

    Product
    Kidoozie™ Play Tents and Playhouses
    Category
    Consumer Product
    Distribution
    Distributed nationwide