The Recall Desk

State

Montana product recalls

73,570 recalls have nationwide distribution and so reach Montana. 3,572 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,572
Critical
689
Severe
952
Most recent
2026-10-14

Of the 3,572 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 952 (27%) are Severe.

Which agencies issued them

These figures cover only the 3,572 recalls whose distribution notice names Montana specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26676–26700 of 77142

  • HighFDA (Devices)·Z-1180-2021·2021-03-17

    Dräger ID Circuit Basic Breathing Circuits Recalled for Detachment Risk

    Dräger Medical is recalling ID Circuit Basic (N) 180 breathing circuits because the Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP01327 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1182-2021·2021-03-17

    Sunstar G.U.M. Hydral Dry Mouth Spray Recalled for Bacterial Contamination

    Sunstar Americas is recalling 56,960 bottles of G.U.M. Hydral Dry Mouth Relief Oral Spray due to potential Burkholderia cepacia contamination.

    Product
    SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray, 2 FL.OZ. UPC0 70942 30713 0 - Product Usage: The device is formulated with water, moisturizers /humectants including one plant-based moisture rich humectant, sweeteners and flavors that collectively have lubricating…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1181-2021·2021-03-17

    Getinge Flow i Anesthesia Systems Recalled for Absorber Docking Failures

    Getinge Group Logistics America is recalling 144 Flow i Anesthesia Systems due to complaints of incorrect FiCO2 readings and System Check Out failures when docking the absorber.

    Product
    Anesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire ventilation of patients with no ability to breathe, as well as in supporting patients with limited ability to breathe.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21097·2021-03-17

    HOFISH Recalls Mattresses for Federal Flammability Standard Violation

    HOFISH is recalling 10-inch hybrid mattresses sold on Amazon.com because they fail to meet the mandatory federal flammability standard, posing a fire hazard.

    Product
    HOFISH 10-Inch Hybrid Certi-PUR Certified Foam and Pocket Spring Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V185000·2021-03-17

    2021 Hyundai Santa Fe Air Bag Child Detection System Defect

    2021 Hyundai Santa Fe vehicles have a defective Occupant Detection System that may fail to prevent air bag deployment when a child restraint is detected in the front passenger seat, increasing crash injury risk.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1178-2021·2021-03-17

    Dräger VentStar Basic Breathing Circuits Recalled for Detachment Risk

    Draeger Medical is recalling 1,525 VentStar Basic breathing circuits because a Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    VentStar Basic (N) 180- Drager Breathing Circuits/Anesthesia Sets Order Number: MP00353 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1187-2021·2021-03-17

    Tosoh Thyroglobulin Antibody Calibrator Recalled for Calibration Failures

    Tosoh Bioscience Inc is recalling specific lots of Thyroglobulin Antibody Calibrators because some combinations with AIA PACKS resulted in unacceptable calibration values.

    Product
    Thyroglobulin Antibody (TgAB) Calibrator - Product Usage: intended for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of anti-thyroglobulin antibodies (TgAb) in human serum on specific TOSOH AIA System analyzers. Measurements obtained by this device aid in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2021·2021-03-17

    Physio-Control Recalls LIFEPAK CR2 Defibrillators Due to Missing Lid Magnets

    Physio-Control is recalling 89,763 LIFEPAK CR2 defibrillators because missing lid magnets may cause premature battery depletion.

    Product
    PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor use in a stationary environment. After the electrode pads are applied, the fully automatic model evaluates the heart rhythm and, if a shockable rhythm is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1188-2021·2021-03-17

    Siemens Dimension Vista HDLC Reagent Cartridges Recalled for Erroneous Results

    Siemens Healthcare Diagnostics is recalling Dimension Vista HDLC reagent cartridges due to discolored reagents that may cause erroneous test results.

    Product
    Dimension Vista HDLC - colorimetric method, lipoproteins - Product Usage: used as an aid in the diagnosis of lipid disorders (such as diabetes mellitus), various liver and renal diseases, and in the assessment of risk for atherosclerosis and cardiovascular disease.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1184-2021·2021-03-17

    MedComp Recalls Power Injectable CT Port Kits with Incorrect Port Size

    Medical Components, Inc. is recalling 96 Power Injectable CT Port kits because they contain 6.6F ports instead of the correct 5F size, which may prolong surgical procedures.

    Product
    Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated access to the vascular system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0299-2021·2021-03-17

    Ferring Recalls Menopur Due to Out-of-Specification pH in Diluent

    Ferring Pharmaceuticals is recalling Menopur (menotropins) and its 0.9% Sodium Chloride diluent because the diluent failed pH specifications. The recall covers products distributed nationwide in the USA.

    Product
    MENOPUR — MENOPUR (MENOTROPINS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1183-2021·2021-03-17

    OraSure Methamphetamine Test Kit Recalled for Incorrect Reagent Lot Labeling

    OraSure Technologies is recalling 16 units of Methamphetamine Intercept Microplate kits due to a labeling error where the wrong lot number was printed on the box.

    Product
    Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination of methamphetamine in oral fluid, PN 11041C.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V180000·2021-03-16

    Jayco Recalls 2021 Embark and Reatta Motorhomes Due to Gas Leak Risk

    Jayco is recalling 2021 Embark and Entegra Reatta motorhomes because an incorrectly routed LP furnace hose may cause a gas leak, increasing the risk of fire or explosion.

    Product
    JAYCO — JAYCO, ENTEGRA EMBARK, REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V181000·2021-03-16

    Peterbilt 536 Recalled for Engine Control Module Software Defect

    PACCAR is recalling one 2021 Peterbilt 536 truck because incorrect engine software may prevent safety features like braking and stability control from functioning properly.

    Product
    PETERBILT — PETERBILT 536
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V179000·2021-03-16

    Highland Ridge RV Recalls Fifth Wheels and Travel Trailers Due to Gas Leak Risk

    Highland Ridge RV is recalling 2019-2020 fifth wheels and travel trailers because an overtightened bolt may damage the stove's O-ring seal, causing a gas leak and increasing fire risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW MESA RIDGE, OPEN RANGE, SILVERSTAR, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V178000·2021-03-16

    2021 Keystone Cougar Trailers Recalled for Electrical Shock Hazard in Inverter

    Certain 2021 Keystone Cougar trailers equipped with the Off the Grid Solar package may have an incorrectly wired inverter that energizes the shore power connection, posing an electrical shock risk. Keystone will repair the inverter at no charge.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V176000·2021-03-15

    2021 BMW 430i and M440i side-thorax airbags may fail to deploy

    2021 BMW 430i and M440i models have defective side-thorax airbags that may not deploy during side-impact crashes, increasing injury risk. Owners should contact their dealer for a free software update.

    Product
    BMW — BMW 430I, M440I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V177000·2021-03-15

    Ditch Witch Trailers Recalled for Missing Side Reflectors

    Charles Machine Works is recalling specific Ditch Witch trailers because they may be missing side reflex reflectors, which reduces visibility to other drivers.

    Product
    DITCH WITCH — DITCH WITCH ZS6S, S4S, 745-7900, 025-1020
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V174000·2021-03-12

    ARBOC Specialty Vehicles Recalls 2021 Spirit of Freedom Due to Fuel Leak

    ARBOC is recalling 29 units of the 2021 Spirit of Freedom because a fuel hose may not be secured correctly, creating a fire risk.

    Product
    ARBOC SPECIALTY VEHICLES — ARBOC SPECIALTY VEHICLES SPIRIT OF FREEDOM
    Category
    Vehicle
    Distribution
    Distributed nationwide