The Recall Desk

State

Illinois product recalls

19,789 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.

5376–5400 of 19789

  • HighFDA (Food)·F-0614-2025·2025-03-19

    Trader Joe's Canned Yellowfin Tuna Recalled for Improperly Sealed Lids

    Trader Joe's Solid Light Yellowfin Tuna is being recalled because the easy-pull lid may not be properly secured, potentially allowing botulism contamination. Approximately 14,147 cases nationwide are affected.

    Product
    Trader Joe's branded Solid Light Yellowfin Tuna in olive oil, Pole & Line Caught; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 51403
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1320-2025·2025-03-19

    ZOLL Powerheart G5 AED may fail self-test in extreme temperatures or humidity

    ZOLL is recalling 73 Powerheart G5 AED units that may fail their internal self-test when exposed to extreme temperatures or humidity. Affected devices could be unreliable in emergencies.

    Product
    Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-01C, (2) G5S-02C, (3) G5S-10C, (4) G5S-11C; Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1319-2025·2025-03-19

    ZOLL Powerheart G5 AED May Fail Self-Test in Extreme Environmental Conditions

    ZOLL is recalling certain Powerheart G5 AED models that may fail their self-test function when exposed to extreme temperature or humidity. Affected devices might not function properly in emergencies.

    Product
    Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-01C, (2) G5A-02C, (3) G5A-05C, (4) G5A-08C, (5) G5A-10C, (6) G5A-13C, (7) G5A-15C, (8) G5A-22C, (9) G5A-41C, (10) G5A-85C, (11) G5A-90C (12) G5A-80-L; Software Version: NA Product Description: The
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0615-2025·2025-03-19

    Trader Joe's Canned Albacore Tuna Recalled for Potential Botulism Contamination

    Trader Joe's Solid White Albacore Tuna is being recalled because the easy-pull lid may not be properly secured, risking contamination with botulism bacteria.

    Product
    Trader Joe's branded Solid White Albacore Tuna in olive oil; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 99287
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0618-2025·2025-03-19

    Trader Joe's Solid White Albacore Tuna Recalled for Botulism Risk

    Trader Joe's branded Solid White Albacore Tuna is being recalled because the easy-pull lids were not properly secured, potentially allowing Clostridium botulinum contamination. Approximately 14,147 cases were distributed nationwide.

    Product
    Trader Joe's branded Solid White Albacore Tuna in water, Low sodium; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 95836
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0616-2025·2025-03-19

    H-E-B Albacore Tuna recalled due to improper lid sealing and botulism risk

    H-E-B branded Solid White Albacore Tuna is being recalled because its easy-pull lid may not be properly secured, risking contamination with Clostridium botulinum. The recalled products were distributed nationwide.

    Product
    HEB branded Solid White Albacore Tuna in water; Wild Caught; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Made with Pride and Care for H-E-B, San Antonio, TX 78204 UPC# 41220 14184 (can); UPC# 41220 43345 (4 pack shrink pack) Chunk White Albacore Tuna in water; wild caught; NET WT.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0611-2025·2025-03-19

    Genova Yellowfin Tuna Cans Recalled for Botulism Risk

    Genova branded Yellowfin Tuna cans are being recalled because the easy-pull lid was not properly secured, which may cause Clostridium botulinum contamination. The recall affects 14,147 cases distributed nationwide with best-by dates from December 2027 through January 2028.

    Product
    Genova branded Yellowfin Tuna; Genova; In Olive Oil; Wild Caught; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 73265 UPC# 48000 13265 UPC# 48000 63267 Product is packaged in several different configurat
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1329-2025·2025-03-19

    Z1 Femoral Hip System Recalled Over Stem Inserter Design Issue

    Zimmer, Inc. is recalling 35 units of the Z1 Femoral Hip System due to a potential design issue with the Z1 Offset Stem Inserter that could cause fracturing of the distal tip.

    Product
    Z1 Femoral Hip System, Product Number 611777612
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1326-2025·2025-03-19

    Beckman Coulter DxI 9000 Analyzer wash wheel mixer defect may prevent operation

    Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to a mechanical defect in the wash wheel mixer that may prevent the device from operating properly. The defect can cause test delays or cancellation.

    Product
    DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1317-2025·2025-03-19

    ZOLL Powerheart G5 AED May Fail Self-Test After Environmental Exposure

    ZOLL Powerheart G5 AED devices may fail their self-test if exposed to extreme temperatures or humidity. Approximately 56,981 units are being recalled nationwide and internationally.

    Product
    Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80A, (2) G5A-80A-TSO. Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0617-2025·2025-03-19

    Genova Yellowfin Tuna Recall: Unsecured Lid May Allow Botulinum Contamination

    Genova branded Yellowfin Tuna in Extra Virgin Olive Oil is being recalled because its easy-pull lid may not be properly secured, potentially allowing clostridium botulinum contamination.

    Product
    Genova branded Yellowfin Tuna in Extra Virgin Olive Oil and Sea Salt; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 13275
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0257-2025·2025-03-19

    Sodium Chloride Injection Recalled for Potential Sterility Compromise

    Nephron Sterile Compounding Center is recalling Sodium Chloride Injection 9% due to potential leakage at the IV bottle port, which could compromise sterility. Affected lots were distributed nationwide.

    Product
    Sodium Chloride Injection 9%, USP, 500 mL, Single-Dose IV Bottle, Rx Only, nephron, 503B outsourcing facility, West Columbia, SC 29172, NDC: 69374-334-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1323-2025·2025-03-19

    ZOLL Powerheart G5 AED Devices Recalled for Self-Test Failure Risk

    ZOLL is recalling 8,744 Powerheart G5 AED units that may fail their self-test if exposed to extreme temperatures or humidity, potentially masking device malfunctions.

    Product
    Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80A; Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrilla
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0273-2025·2025-03-19

    Acne treatment gel recalled for benzene contamination nationwide

    Zapzyt Acne Treatment Gel (10% benzoyl peroxide) distributed nationwide is being recalled due to contamination with benzene. Consumers should stop using affected lots immediately.

    Product
    ZAPZYT ACNE TREATMENT GEL — ZAPZYT ACNE TREATMENT GEL (BENZOYL PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1314-2025·2025-03-19

    COR Disposable Cartilage Transplant Kit recalled for missing graft loader pin

    DePuy Mitek's COR Disposable Cartilage Transplant System is being recalled because some units are missing a pin in the graft loader component, which could affect surgical function.

    Product
    COR Disposable Kit, 8 mm. Cartilage Transplant System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0274-2025·2025-03-19

    Walgreens Acne Control Cleanser recalled for benzene contamination

    Walgreens Acne Control Cleanser with 10% benzoyl peroxide is being recalled nationwide due to benzene contamination. The affected lot (23-09328, exp. 09/2025) was distributed across the U.S.

    Product
    Walgreens, Acne Control Cleanser, 10% Benzoyl Peroxide/Acne Treatment, NET WT 5 OZ (142g) Distributed by: Walgreen CO, 200 Wilmont RD, Deerfield, IL, Made in Canada. UPC#: 1 9560203602 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1308-2025·2025-03-19

    Hemostatic Forceps Recalled Due to Clamp Breakage in Surgical Use

    Aesculap Inc is recalling 19,979 hemostatic forceps across 18 models because clamps can break when instruments are used outside of design specifications.

    Product
    Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf Hysterectomy Forceps STR 210MM; (2) REF BJ501R, Phaneuf Hysterectomy Forceps ANG 205MM; (3) REF BJ511R, Holzbach Hyst Forceps CVD245MM; (4) REF BJ520R, Heaney Hyst Forceps Grooved 205MM; (5) REF BJ52
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1327-2025·2025-03-19

    Blood Pump Recalled for Potential Fluid Leakage During Clinical Use

    Spectrum Medical is recalling Quantum Perfusion blood pumps due to potential fluid leakage during priming or clinical use. The issue affects approximately 1,487 units distributed nationwide.

    Product
    Brand Name: Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors Product Name: Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type Model/Catalog Number: CP22V-VT Software Version: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0275-2025·2025-03-19

    Kids by Babyganics SPF 50 Sunscreen Recalled for Chemical Contamination

    Kids by babyganics SPF 50 sunscreen is being recalled due to chemical contamination. Approximately 449,502 units distributed nationwide in the U.S. and Canada are affected in this FDA Class II recall.

    Product
    Kids by babyganics SPF 50 totally tropical (titanium dioxide 3/5%, zinc oxide 7.25%) packaged in a) 6 OZ (170 g) spray bottles UPC 813277019954 and UPC 813277019800; and b) Twinpack UPC 813277019930; Dist. by KAS Direct LLC, 1525 Howe St. Racine, WI 53403.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·25169·2025-03-13

    Sublue Mix Underwater Scooters Recalled for Lithium-Ion Battery Fire Hazard

    Sublue is recalling about 40,370 Mix underwater scooters and batteries with lithium-ion cells that can overheat and catch fire. Reports include 8 fires, 1 injury, and significant property damage.

    Product
    Sublue Mix underwater scooters and replacement batteries (black batteries only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25182·2025-03-13

    Onasti Toddler Tower Stools Recalled for Fall and Injury Risk

    Onasti Toddler Tower Stools sold on Amazon can collapse or tip over while in use, posing fall and injury risks. Recalls follow four reports of incidents, including injuries.

    Product
    Onasti Toddler Tower Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25178·2025-03-13

    Retractable Safety Gates Recalled for Risk of Child Entrapment

    HabiLife Direct retractable safety gates (model SG021) are recalled due to an entrapment hazard where children's torsos can fit through gaps between the gate and floor. About 880 units sold on Amazon from September 2024 through January 2025.

    Product
    Retractable Safety Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25179·2025-03-13

    Meijer Recalls Konwin Desktop Heaters Due to Fire and Burn Hazards

    Meijer is recalling about 6,050 Konwin desktop heaters because the fan can fail to turn on, causing the unit to overheat and ignite. The company received eight reports of fans burning and melting, but no injuries have been reported.

    Product
    Konwin Desktop Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25180·2025-03-13

    Chews Life Recalls Silicone Rosary and Decade Teethers for Choking Hazard

    About 5,700 Chews Life Silicone Rosary and Decade teethers are being recalled because the safety snap clasp can detach, posing a choking hazard to infants. No injuries have been reported.

    Product
    Silicone Rosary and Decade teethers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25183·2025-03-13

    Gerolsteiner Sparkling Water Bottles Recalled Due to Laceration Hazard

    Gerolsteiner 750ml sparkling water bottles sold at Trader Joe's locations are being recalled because the glass bottles can crack, creating a laceration hazard. No injuries have been reported.

    Product
    Gerolsteiner 750ml Sparkling Water Bottles
    Category
    Food
    Distribution
    Distributed nationwide