The Recall Desk

State

Montana product recalls

72,969 recalls have nationwide distribution and so reach Montana. 3,568 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,568
Critical
689
Severe
783
Most recent
2026-09-16

Of the 3,568 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.

Which agencies issued them

These figures cover only the 3,568 recalls whose distribution notice names Montana specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5876–5900 of 76537

  • ModerateFDA (Food)·H-0381-2025·2025-08-06

    Pure Monk Fruit Sweetener bottles actually contain mislabeled stevia powder

    Pure Monk Fruit Sweetener, 0.71 oz, is being recalled because the product is stevia powder but the bottle was mislabeled as Pure Monk Fruit Sweetener. 78 bottles are affected.

    Product
    Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187 6. Product is packaged in a plastic bottle with white cap. Ingredient: Monk Fruit (Luo Han Guo) Extract. Monk Fruit is so much sweeter than sugar, a pinch is all you need. Suggested Use: Add to sweeten your food or be
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2197-2025·2025-08-06

    IontoPatch 80 nonwoven pads do not absorb the saline solution

    IontoPatch 80 On-the-Go Patch Therapy is being recalled because the nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with it. 63,936 units affected.

    Product
    IontoPatch 80, On-the-Go Patch Therapy, Model/Catalog Number: D-0077-080; The IontoPatch is an Iontophoresis transdermal patch.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2219-2025·2025-08-06

    ASPIRE Cristalle mammography systems shipped with unapproved slabbing software enabled

    ASPIRE Cristalle Mammography Systems with the Digital Breast Tomosynthesis option are being recalled because devices had an unapproved slabbing software function enabled for use. 293 units affected.

    Product
    ASPRIRE Cristalle Mammography System (cleared under K212873) installed with the ASPIRE Cristalle Digital Breast Tomosynthesis (DBT) Option (approved under P160031).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0380-2025·2025-08-06

    Organic Pure Stevia bottles actually contain mislabeled monk fruit powder

    Organic Pure Stevia, 1 oz, is being recalled because the product is monk fruit powder but the bottle was mislabeled as Organic Pure Stevia. 78 bottles are affected.

    Product
    Organic Pure Stevia, net wt. 1oz. UPC 7 39223 00204 0. Product is packaged in a plastic bottle with white cap. Ingredient: Organic Stevia Extract. Sprinkle a pinch for the perfect sweetness. Suggested Use: 1/64 tsp tastes as sweet as 1 tsp of sugar. Distributed by: NuNaturals, I
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2196-2025·2025-08-06

    IontoPatch STAT nonwoven pads do not absorb the saline solution

    IontoPatch STAT On-the-Go Patch Therapy is being recalled because the nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with it. 80,928 units affected.

    Product
    IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2172-2025·2025-08-06

    Sterilizable Drill Stop Kits were shipped containing incorrect components

    The Drill Stop Kit, a version of the Mini Sterilizable Tray used to store, sterilize and verify drill stop length, is being recalled because it contains incorrect components. 45 kits affected.

    Product
    The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop length, and facilitate the mounting/removal of the Drill Stops. The Drill Stop Kit includes the Release Bracket, which is used for mounting and removing Drill Stops
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V501000·2025-08-05

    2024–2026 International LT and 2025 RH Trucks Service Brake Defect

    International Motors is recalling certain 2024–2026 LT and 2025 RH trucks because the Hill Start Assist exhaust port may clog, preventing brake release and increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL LT, RH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E049000·2025-08-05

    Holley Recalls 140 GPH Electric Fuel Pumps Due to Methanol Incompatibility

    Holley Performance Products is recalling 140 GPH BLACK electric fuel pumps because they may not be compatible with methanol fuel, which can cause leaks and fire risks.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V499000·2025-08-04

    2024-2025 Winnebago Ekko RV Tire Valve Extension Defect Recall

    Winnebago is recalling certain 2024-2025 Ekko recreational vehicles due to damaged tire valve extensions that can cause air loss in the inner tire and overload the outer tire, creating a crash risk. Dealers will replace the extensions free of charge.

    Product
    WINNEBAGO — WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E048000·2025-08-01

    Bendix Recalls Knorr-Bresme Brake Chambers for Fire Risk

    Bendix is recalling specific Knorr-Bresme brake chambers for buses due to improper manufacturing that can cause air leaks and increase fire risk.

    Product
    PARKING BRAKE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·25415·2025-07-31

    KidKraft play kitchen hooks caused a toddler's fatal strangulation in Oregon

    KidKraft Farm to Table play kitchens are being recalled because clothing can catch on the accessory hooks. A 23-month-old child died from strangulation and asphyxia in February 2023.

    Product
    KidKraft Farm to Table Model Play Kitchen
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25412·2025-07-31

    Cosco two-step kitchen stepper safety bars can detach or break

    The Cosco 2-Step Kitchen Stepper is being recalled because the safety bar can detach or break while in use. Thirty-four reports include two incidents resulting in head injuries.

    Product
    Cosco 2-Step Kitchen Stepper
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25420·2025-07-31

    IKEA VÄRDEFULL garlic presses can shed small metal pieces

    IKEA 365+ VÄRDEFULL garlic presses are being recalled because small metal pieces can detach, posing laceration and ingestion hazards. Three lacerations have been reported globally.

    Product
    IKEA 365+ VÄRDEFULL garlic presses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25413·2025-07-31

    Tegu magnetic floating stacker toys can shed high-powered magnets

    Tegu Magnetic Floating Stackers are being recalled because magnets can loosen and detach, violating the mandatory standard for toy magnets. Thirty-one reports of magnets separating have been received.

    Product
    Magnetic Floating Stackers toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25416·2025-07-31

    RIDGID brushless framing nailers can discharge a nail from the trigger alone

    RIDGID 18Volt Brushless 21-Degree and 30-Degree Framing Nailers are being recalled because the dual action engagement system can malfunction and involuntarily discharge a nail. About 64,000 units affected.

    Product
    RIDGID 18Volt Brushless 21-Degree Framing Nailers and RIDGID 18Volt Brushless 30-Degree Framing Nailers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V496000·2025-07-31

    Premier Trailer Recalls 2024 Reel and Pole Trailers Due to Brake Oil Leak

    Premier Trailer Solutions is recalling 2024 Reel and Pole trailers because improperly installed oil seals may leak oil onto the brake system, reducing braking ability.

    Product
    PREMIER TRALER — PREMIER TRALER REEL TRAILER, POLE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V498000·2025-07-31

    Storyteller Overland Recalls 2023 Mode LT RVs Due to Shore Power Fire Risk

    Storyteller Overland is recalling 2023 Mode LT recreational vehicles because improperly tightened shore power inlets may overheat and cause a fire. Dealers will replace the inlets free of charge.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND MODE LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25414·2025-07-31

    Leatherman Charge Plus multi-tool knife blades do not fully fold in

    Leatherman Charge Plus and Charge Plus TTi multi-tools are being recalled because the tip of the knife blade does not fully fold into the handle, posing a laceration hazard. About 17,000 units affected.

    Product
    Leatherman Charge Plus and Charge Plus TTi Multi-Tools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2166-2025·2025-07-30

    Biofinity Toric Multifocal contact lens blisters may have a leaking seal

    Biofinity Toric Multifocal Contact Lenses are being recalled because lens blisters may have an incomplete or leaking seal, which may render them unsterile. 827 units are affected.

    Product
    Biofinity Toric Multifocal Contact Lens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V497000·2025-07-30

    Brinkley trailer wiring may be unsecured risking a short circuit

    Brinkley RV is recalling certain 2025 Model Z trailers because the electrical wiring may not be secured properly, which can damage the wiring and cause a short circuit.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2168-2025·2025-07-30

    SmartSync Patient Connector limited the window to abort high voltage therapy

    The Medtronic CareLink SmartSync Patient Connector is being updated because in prior application versions the abort window during an induction test limited the user's ability to cancel high voltage therapy. 22,091 devices affected.

    Product
    Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Crome application, Software Model Number D00U005; 2. Claria Amplia Compia application, Software Model Number D00U009; 3. Evera MRI application, Software M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2133-2025·2025-07-30

    SIGNA PET/MR gradient coils can produce acoustic noise above the limit

    GE HealthCare SIGNA PET/MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    SIGNA PET/MR
    Category
    Medical Device
    Distribution
    Distributed nationwide