The Recall Desk

State

Montana product recalls

72,820 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 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26–50 of 76387

  • HighCPSC·26740·2026-09-03

    Truststone Recalls XO Poppy Magnetic Wireless Power Banks Due to Fire Hazards

    Truststone Group is recalling XO Poppy Power Trip Magnetic Wireless Power Banks because the lithium-ion batteries can overheat and ignite, posing fire and burn risks.

    Product
    XO Poppy Power Trip Magnetic Wireless Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E062000·2026-09-03

    Nova Bus Recalls Casco Engine Coolant Level Sensors

    Nova Bus is recalling Casco engine coolant level sensors that may send false signals, causing unexpected engine shutdowns and increasing crash risk.

    Product
    ENGINE AND ENGINE COOLING:COOLING SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26739·2026-09-03

    Skip Hop Recalls Elmo Silicone Teethers Due to Choking Hazard

    Skip Hop is recalling Baby Sesame Street Elmo Silicone Teethers because the black eyes can detach if frozen, posing a choking risk.

    Product
    Baby Sesame Street Elmo Silicone Teethers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26741·2026-09-03

    Clorox Recalls Scented Mistolin and Lestoil Cleaners in Puerto Rico

    Clorox is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands due to potential bacterial contamination.

    Product
    Scented Mistolin® Dilutable Cleaners and Lestoil® Heavy Duty Multi-Purpose Cleaners sold in Puerto Rico and the U.S. Virgin Islands.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1273-2026·2026-09-02

    Botticelli Foods Recalls Pistachio Nut Butter Due to Salmonella Risk

    Botticelli Foods is recalling bettergoods brand Pistachio Nut Butter because it may be contaminated with Salmonella. The recall affects 16,200 units distributed across 19 states.

    Product
    bettergoods brand Pistachio Nut Butter, NET WT 6.7oz (190g), UPC 194346207961
    Category
    Food
    Distribution
    19 states
  • SevereFDA (Drugs)·D-0785-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 200 mcg tablets because they are subpotent. The recall covers distribution nationwide in the United States.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0790-2026·2026-09-02

    Zicam Cold Remedy Nasal Swabs Recalled for Microbiological Testing Failures

    Church & Dwight is recalling Zicam Cold Remedy Nasal Swabs because FDA inspections found out-of-limit microbiological testing results at the contract manufacturer.

    Product
    Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free Homeopathic, Distributed by Church & Dwight Co. Inc., Ewing, NJ 08628, UPC 732216301205.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0779-2026·2026-09-02

    Accord Healthcare Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 100 mcg tablets because they may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0803-2026·2026-09-02

    ACTHAR Gel Recalled for Presence of Glass and Stopper Particulate Matter

    Mallinckrodt is recalling ACTHAR Gel vials due to the presence of glass and stopper pieces. Patients should stop using the product and contact their healthcare provider.

    Product
    ACTHAR — ACTHAR (REPOSITORY CORTICOTROPIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0778-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0776-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 50 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2991-2026·2026-09-02

    Medline Neonatal Heated Wire Breathing Circuits Recalled for Thermal Failure

    Medline is recalling 20 units of neonatal heated wire breathing circuits due to potential thermal damage that could cause airway obstruction or respiratory distress in infants.

    Product
    Medline Hudson RCI, DBD-CIRCUIT,VENT,INSPIRATORY,HEATED,NEO, Medline Product Number/SKU HUD78019 (Teleflex Product Number/SKU 780-19); breathing circuit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0832-2026·2026-09-02

    B. Braun Recalls Lactated Ringer's Injection Due to Particulate Matter

    B. Braun Medical Inc. is recalling 23,688 bags of Lactated Ringer's Injection USP due to the presence of particulate matter.

    Product
    LACTATED RINGERS — LACTATED RINGERS (SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0786-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling Levothyroxine Sodium 300 mcg tablets because they may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2993-2026·2026-09-02

    Medline Neonatal Heated Wire Breathing Circuits Recalled for Thermal Damage Risk

    Medline is recalling neonatal and infant heated wire breathing circuits due to a risk of sporadic failure and thermal damage at the humidifier connector.

    Product
    Medline breathing circuits labeled as: 1) MEDLINE HUDSON RCI, CIRCUIT, NEO, SING LIMB, HTD,COLUMN, Medline Product Number/SKU HUD78001KIT (Teleflex Product Number/SKU 780-01KIT); 2) MEDLINE HUDSON RCI, CIRCUIT, NEO, DUAL LIMB HTD, COLUMN, Medline Product Number/SKU HUD78007K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0827-2026·2026-09-02

    Fresenius Kabi Recalls Tyenne Injection Due to Glass Particles

    Fresenius Kabi is recalling Tyenne (tocilizumab-aazg) injection vials because an internal investigation found the presence of glass particles.

    Product
    TYENNE — TYENNE (TOCILIZUMAB-AAZG)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V570000·2026-09-02

    Toyota Recalls 2026 C-HR Vehicles Due to Battery Overcharge Risk

    Toyota is recalling 8,521 2026 C-HR battery electric vehicles because a software error may cause the battery to overcharge, potentially leading to a loss of drive power and increased crash risk.

    Product
    TOYOTA — TOYOTA C-HR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3027-2026·2026-09-02

    Medline Recalls Surgical Convenience Kits Due to Contaminated Components

    Medline Industries is recalling 169 surgical convenience kits nationwide because they contain potentially contaminated components.

    Product
    Medline convenience kits labeled as: 1) LAVH, Medline Kit SKU CDS982273U; 2) GYN ABDOMINAL CDS, Medline Kit SKU CDS982654L; 3) GYN LAP HYSTERECTOMY CDS, Medline Kit SKU CDS982662Q; 4) CMH VAG HYSTERECTOMY PK-LF, Medline Kit SKU DYNJ54382F; 5) A P RESECTION, Medline Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3029-2026·2026-09-02

    Medline Recalls Neurosurgical Convenience Kits Due to Contamination

    Medline Industries is recalling 241 neurosurgical convenience kits distributed nationwide because they contain a potentially contaminated component.

    Product
    Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104; 3) CRANIOTOMY, Medline Kit SKU DYNJ903471I; 4) KIT CRANIOTOMY RFD, Medline Kit SKU DYNJ906496K.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2997-2026·2026-09-02

    Medline Neurosurgical Kits Recalled for Endotoxin Contamination

    Medline is recalling 974 neurosurgical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.

    Product
    Medline medical convenience kits, labeled as: 1) LAMINECTOMY PACK, Medline Kit SKU DYNJT6548; 2) ORTHO SPINE PACK, Medline Kit SKU DYNJ44504G; 3) NEURO SPINE PACK, Medline Kit SKU DYNJ45419F; 4) CRANIOTOMY PACK, Medline Kit SKU DYNJ46024F; 5) SPINE PACK, Medline Kit SK
    Category
    Medical Device
    Distribution
    Distributed nationwide