The Recall Desk

State

Montana product recalls

72,940 recalls have nationwide distribution and so reach Montana. 3,567 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,567
Critical
689
Severe
783
Most recent
2026-09-02

Of the 3,567 recalls naming Montana we have scored against our rubric, 689 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 783 (22%) are Severe.

These figures cover only the 3,567 recalls whose distribution notice names Montana specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4001–4025 of 76507

  • CriticalFDA (Devices)·Z-0586-2026·2025-12-10

    Infusion pump administration sets recalled over incorrect assembly of one lot

    Fresenius Kabi USA is recalling 483 cases of Ivenix LVP Primary Administration Sets after incorrect assembly of a specific lot that the firm states could result in serious patient injury.

    Product
    IVENIX INFUSION SYSTEM, LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Large Volume Infusion Pump Administration Set.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0725-2026·2025-12-10

    Fecal immunochemical tests recalled over the potential for false negative results

    Enterix is recalling 201,426 InSure ONE Fecal Immunochemical Test kits after the test failed sensitivity testing with one test card lot, which may result in false negative results.

    Product
    InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure ONE POL Patient Kit - 10 pack. Model Number: 90010. 2. Insure ONE POL Patient Kit - 25 Pack. Model Number: 90025. 3. InSure ONE POL Combo Pack. Model Number: 90030. InSure ONE is a fecal immunochemica
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0859-2026·2025-12-10

    IntelliVue X2 measurement servers recalled over a potential failure to alarm

    Philips North America is recalling the IntelliVue Multi Measurement Server X2 over a potential issue where the monitors did not alarm.

    Product
    IntelliVue Multi Measurement Server X2. Product Number: M3002A.
    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
  • HighFDA (Food)·H-0213-2026·2025-12-10

    Bladder supplement recalled over potential contamination with two E. coli strains

    Water Pure is recalling 17,612 bottles of My Bladder dietary supplement because the product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303.

    Product
    My Bladder; Supports normal bladder tone & control; Dietary Supplement; packaged in white HDPE bottle with a white cap; bottle size is 150 CC; the net contents in 60 clear capsules containing brown powder
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·25V853000·2025-12-10

    MCI Transit Buses Recalled for Incorrect Front Door Glazing Material

    Motor Coach Industries is recalling various transit bus models because the front door lower curb view glazing material is incorrect, which may reduce driver visibility and increase crash risk.

    Product
    MCI — MCI D4005, J4500, J3500, E4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V851000·2025-12-10

    Blue Bird Recalls School Buses With Defective Wheelchair Restraints

    Blue Bird is recalling 2026-2027 Vision and All American school buses because wheelchair restraints may fail to lock, increasing injury risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS, VISION SCHOOL BUS (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide