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.

8051–8075 of 84599

  • 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 (Food)·F-0630-2025·2025-03-19

    Ulker Kekstra strawberry cookies recalled for undeclared milk allergen

    Ulker Kekstra Mini strawberry cookies are recalled for undeclared milk allergen. Consumers with milk allergies should not consume this product.

    Product
    Ulker Kekstra Mini strawberry, item 3792, 5.3oz foil pack, 10 per case, UPC 8690766082307
    Category
    Food
    Distribution
    36 states
  • HighFDA (Devices)·Z-1328-2025·2025-03-19

    Stryker CinchLock anchor recalled due to pullwire breakage

    Stryker is recalling its CinchLock Flex Knotless Anchor due to an increase in pullwire breakage complaints. The broken pullwire may remain in the implant body after deployment.

    Product
    Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197
    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 (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 (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-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 (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 (Devices)·Z-1321-2025·2025-03-19

    ZOLL Powerheart G5 AED devices may fail self-test in extreme environments

    ZOLL is recalling Powerheart G5 AED devices that may fail their self-test when exposed to extreme temperature or humidity, potentially affecting proper device operation.

    Product
    Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80C; 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 (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
  • 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
  • SevereNHTSA·25V170000·2025-03-18

    Tesla Cybertruck light bar can delaminate and detach from vehicle

    Tesla is recalling certain 2024-2025 Cybertruck vehicles because the light bar can delaminate and detach, becoming a road hazard for other traffic.

    Product
    TESLA — TESLA CYBERTRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V163000·2025-03-14

    Ford Super Duty steering column shifters may be improperly welded

    Ford is recalling certain 2025 Super Duty F-250, F-350 and F-450 vehicles because the steering column shifter may have been improperly welded and detach from the column.

    Product
    FORD — FORD F-350 SD, F-450 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V162000·2025-03-14

    Forest River Recalls 2025 Nightfall and XLR Trailers Due to Brake Wiring

    Forest River is recalling 2025 Nightfall and XLR Toy Hauler trailers because the breakaway switch may be incorrectly wired, preventing trailer brakes from activating in an emergency.

    Product
    FOREST RIVER — FOREST RIVER NIGHTFALL, XLR TOYHAULER 5TH WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V167000·2025-03-14

    Mazda CX-50 trailer hitch bolts may loosen and separate the assembly

    Mazda is recalling certain 2024-2025 CX-50 vehicles with genuine accessory trailer hitches because the assembly bolts may loosen and the hitch separate from the vehicle body.

    Product
    MAZDA — MAZDA CX-50 HYBRID, CX-50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V169000·2025-03-14

    Ford Recalls 2021 F-150s for Transmission Software Update

    Ford is recalling 2021 F-150 vehicles previously repaired under recall 22V-188 because a software error may cause the transmission to unexpectedly shift into neutral, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V157000·2025-03-14

    Ford Super Duty window reversal repair under an earlier recall was incorrect

    Ford is recalling certain 2023 Super Duty F-250 and F-350 vehicles previously repaired incorrectly under recall 23V-507, because the front windows may not reverse on an obstruction.

    Product
    FORD — FORD F-350 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V160000·2025-03-14

    Ford Edge rearview camera repair under an earlier recall was incorrect

    Ford is recalling certain 2021-2022 Edge vehicles previously repaired incorrectly under recall 22V-151, because a software error may blank or distort the rearview camera image.

    Product
    FORD — FORD EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V165000·2025-03-14

    Ford Escape fuel injector repair under earlier recalls was incorrect

    Ford is recalling certain Escape and Bronco Sport vehicles previously repaired incorrectly under recalls 22V-859 or 24V-187, because a fuel injector may crack and leak fuel.

    Product
    FORD — FORD BRONCO SPORT, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V159000·2025-03-14

    Ford Explorer and Aviator camera video output may fail entirely

    Ford is recalling certain Explorer, Lincoln Aviator and Corsair vehicles previously repaired incorrectly under recall 23V-342, because the video output may fail.

    Product
    FORD — FORD, LINCOLN EXPLORER, CORSAIR, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V164000·2025-03-14

    Ford transmission valve bodies may have been machined incorrectly

    Ford is recalling certain 2024-2025 vehicles because the transmission valve body may have been machined incorrectly, causing reverse gear failure or unexpected forward movement.

    Product
    FORD — FORD, LINCOLN F-150, EXPLORER, RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide