The Recall Desk

State

Ohio product recalls

72,940 recalls have nationwide distribution and so reach Ohio. 11,719 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total
11,719
Critical
2,106
Severe
2,413
Most recent
2026-09-09

Of the 11,719 recalls naming Ohio we have scored against our rubric, 2,106 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,413 (21%) are Severe.

Which agencies issued them

These figures cover only the 11,719 recalls whose distribution notice names Ohio specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4201–4225 of 84659

  • HighFDA (Food)·H-0233-2026·2025-12-10

    Prenatal chewable vitamins recalled over undeclared soy and a boron labeling error

    Avion Pharmaceuticals is recalling 804 bottles of Prenate Chewable after positive test results for soy, which is not listed on the label, and a boron amount stated in mg instead of mcg.

    Product
    Prenate Chewable¿ A chewable Rx prenatal vitamin with a delicious chocolate flavor with Quatrefolic Dietary Supplement 30 Tablets Rx Only UPC 3 75854 30630 2 Manufactured for: Avion Pharmaceuticals, LLC Alpharetta, GA 30005
    Category
    Drug
    Distribution
    17 states
  • HighFDA (Devices)·Z-0866-2026·2025-12-10

    IntelliVue MX600 patient monitors recalled because an alarm may not sound

    Philips North America is recalling the IntelliVue Patient Monitor MX600 over a potential issue where the monitors did not alarm.

    Product
    IntelliVue Patient Monitor MX600. Product Number: 865242.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0858-2026·2025-12-10

    IntelliVue MP90 monitors recalled because an alarm may not sound

    Philips North America is recalling the IntelliVue MP90 over a potential issue where the monitors did not alarm.

    Product
    IntelliVue MP90. Product Number: M8010A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0871-2026·2025-12-10

    Fibula nails recalled over out of specification thread depths on the implant

    Paragon 28 is recalling 20 Phantom Fibula Nails because out of specification thread depths may prevent the implant from mating with its mounting bolt, potentially requiring surgery to be aborted.

    Product
    Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0884-2026·2025-12-10

    DNA sequencing reagent kits recalled over flow cell gasket leaks

    Illumina is recalling 11,916 NextSeq 550Dx reagent kits because flow cell gaskets have a quality issue that may cause leaks during runs, including possible toxic substance exposure to the user.

    Product
    Reagent Kits/ containing flow cells, components of NextSeq 550Dx Instrument: NextSeq 550Dx High Output Reagent Kit v2.5 (75 cycles) IVD, REF: 20028870/NextSeq 550Dx HO FC Cart v2.5, 75 Cycles, REF: 20031098; NextSeq 550Dx High Output Reagent Kit v2.5 (300 cycles) IVD, REF: 2002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V852000·2025-12-10

    Blue Bird Recalls Vision School Buses Due to Wheelchair Lift Defect

    Blue Bird is recalling 2025-2027 Vision school buses because a missing support brace may cause the wheelchair lift to fail, increasing injury risk.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0861-2026·2025-12-10

    DHEA tests recalled for distribution without premarket approval or clearance

    Get Tested International AB is recalling 17 units of its DHEA Test because the product was distributed without premarket approval or clearance.

    Product
    IntelliVue Patient Monitor MX100. Product Number: 867033.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0204-2026·2025-12-10

    Wound hydrogel recalled over current good manufacturing practice deviations

    Blossom Pharmaceuticals is recalling 8,184 bottles of Dynagel Moisturizing Wound Hydrogel over current good manufacturing practice deviations.

    Product
    Dynagel, Moisturizing Wound Hydrogel, Net Wt. 3oz (84.7 g), Manufactured for: Dynarex Corporation, 16 Glenshaw Street, Orangeburg, NY 10962, UPC 61784128016.
    Category
    Drug
    Distribution
    Distributed nationwide