The Recall Desk

State

Illinois product recalls

72,919 recalls have nationwide distribution and so reach Illinois. 11,602 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total
11,602
Critical
2,039
Severe
2,515
Most recent
2026-09-09

Of the 11,602 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 2,515 (22%) are Severe.

These figures cover only the 11,602 recalls whose distribution notice names Illinois specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2551–2575 of 84521

  • HighFDA (Drugs)·D-0440-2026·2026-04-15

    Fagron vancomycin 1.25 gram bags recalled over sterility and detaching port part

    Fagron is recalling Vancomycin HCl 1.25 grams in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.

    Product
    Vancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5083-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0439-2026·2026-04-15

    Fagron norepinephrine 32 mg bags recalled over sterility and port part

    Fagron is recalling norepinephrine bitartrate 32 mg in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.

    Product
    norepinephrine Bitartrate, 32mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5027-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0438-2026·2026-04-15

    Fagron norepinephrine infusion bags recalled over sterility and detaching port part

    Fagron is recalling norepinephrine bitartrate 16 mg in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.

    Product
    norepinephrine Bitartrate,16mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5026-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1774-2026·2026-04-15

    Molded Products Luer cap sets recalled after threaded sleeve detachment complaint

    Molded Products is recalling the MPC-130 See Luer Cap Set following a confirmed complaint that the threaded sleeve was not engaged and became detached. 26,900 units are affected.

    Product
    See Luer Cap Set, MPC-130, set, administration, intravascular
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0663-2026·2026-04-15

    Vital Nutrients Aller-C supplement recalled for undeclared allergens

    Blueroot Health, Inc. is recalling Vital Nutrients Aller-C vitamin supplements because they contain undeclared egg, soy, and hazelnut allergens, posing a risk to consumers with allergies to these ingredients.

    Product
    Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count bottles
    Category
    Food
    Distribution
    40 states
  • HighFDA (Devices)·Z-1795-2026·2026-04-15

    Preeclampsia growth factor assay recalled over out-of-range quality control values

    B.R.A.H.M.S PlGF Plus KRYPTOR in vitro diagnostic tests are being recalled after customers observed out-of-range values at the lowest quality control level, which can contribute to falsely elevated results.

    Product
    B¿R¿A¿H¿M¿S KRYPTOR compact REACT, REF: 89986, used with B¿R¿A¿H¿M¿S PlGF Plus KRYPTOR, REF: 859075N, and run on the B¿R¿A¿H¿M¿S KRYPTOR compact PLUS analyzers. in vitro diagnostic test for Placental Growth Factor
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Drugs)·D-0442-2026·2026-04-15

    Fagron vancomycin infusion bags recalled over sterility and detaching port part

    Fagron Sterile Services is recalling Vancomycin HCl 1 gram in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.

    Product
    Vancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5082-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0430-2026·2026-04-15

    Fresenius Kabi 100 mL sodium chloride bags for BD recalled over sterility

    Fresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP in 100 mL single dose freeflex bags distributed by BD, citing lack of assurance of sterility.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0428-2026·2026-04-15

    Fresenius Kabi 500 mL saline freeflex bags recalled over sterility assurance

    Fresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP supplied in 500 mL freeflex bags under its own label, citing lack of assurance of sterility.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0651-2026·2026-04-15

    Zarlengo's chocolate gelato omits soy from the contains statement

    Zarlengo's Chocolate Gelato is being recalled because soy lecithin appears in the ingredients statement but soy is not declared in the contains statement.

    Product
    Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminated with heat-sealable plastic, 16 fl
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1793-2026·2026-04-15

    Multi-parameter command modules may produce inaccurate cardiac output readings

    A circuit board issue in Multi-parameter Command Module model 91496 can start cardiac output measurement early in Auto mode, producing errors and inaccurate readings. 1,790 units are affected.

    Product
    Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1653-2026·2026-04-15

    Siemens ARTIS imaging systems may display an inflated patient dose reading

    Siemens ARTIS pheno and ARTIS Icono systems may sporadically display a major increase in the x-ray dose applied, although the actual dose applied remains within system settings and regulatory limits.

    Product
    ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V238000·2026-04-14

    Ford Recalls 2024-2026 Rangers for Sun Visor Wiring Fire Risk

    Ford is recalling 2024-2026 Ranger vehicles because improperly positioned sun visor or headliner wiring harnesses may cause an electrical short and fire in the A-pillar area.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V235000·2026-04-14

    Ford F-59 front axle hub may be missing its spindle nut

    Ford is recalling certain 2025-2026 F-59 and F-53 vehicles because the front axle hub assembly may be missing the spindle nut and cotter pin, which can lead to wheel detachment.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V237000·2026-04-14

    Ford Recalls 2015-2017 F-150 Trucks for Transmission Software Defect

    Ford is recalling 2015-2017 F-150 vehicles because a signal loss can cause unexpected downshifting, increasing crash risk. Dealers will update software free of charge.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V236000·2026-04-14

    Ford Bronco transfer case joint misalignment may wear driveline splines

    Ford is recalling certain 2021-2025 Bronco vehicles because a misaligned transmission to transfer case joint can wear the splines, potentially causing loss of drive power or rollaway.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V239000·2026-04-14

    2026 Ford Bronco Sport Engine Block Heater Fire Risk Recall

    Ford is recalling certain 2026 Bronco Sport vehicles with a 1.5L or 2.0L MPC engine and block heater because the heater may overheat when plugged in while parked, increasing fire risk.

    Product
    FORD — FORD MAVERICK, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V234000·2026-04-13

    2025–2026 Harley-Davidson Softail motorcycles rear brake line defect

    Harley-Davidson is recalling certain 2025–2026 Softail motorcycles because the rear brake line may contact the Body Control Module, causing a brake fluid leak and loss of rear brakes. Loss of rear brakes increases crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHC, FXBB, FXLRS, FXLRST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V232000·2026-04-10

    2022–2026 Kia Carnival vehicles recalled for fuel system leak risk

    Kia is recalling certain 2022–2026 Carnival vehicles because fuel may leak at the pipe connection between the fuel pipe and fuel rail, increasing the risk of fire.

    Product
    KIA — KIA CARNIVAL
    Category
    Vehicle
    Distribution
    Distributed nationwide