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.

476–500 of 76387

  • SevereNHTSA·26V500000·2026-07-30

    Honda Motorcycles Recalled Due to Handlebar Lock Screw Risk

    Honda is recalling certain CMX300, CMX500, and SCL500 motorcycles because the handlebar lock screw may loosen and detach, potentially interfering with steering.

    Product
    HONDA — HONDA CMX500, CMX300, SCL500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V498000·2026-07-30

    Winnebago Ekko Motorhomes Recalled Over Generator Software Fault

    Winnebago is recalling certain 2024-2025 Ekko motorhomes because the touchscreen display may register unintended inputs and turn the generator on without the operator's knowledge.

    Product
    WINNEBAGO — WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V494000·2026-07-30

    2026 Cadillac, GMC, and Chevrolet electric vehicles recalled due to battery fire risk

    General Motors is recalling certain 2026 Cadillac Escalade, GMC Sierra EV, and Chevrolet Silverado EV models because an improperly secured battery component may increase the risk of a fire.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE IQ, ESCALADE IQL, SILVERADO EV, SIERRA EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26658·2026-07-30

    Woodure toddler kitchen step stools recalled after 22 tip-over reports

    About 91,000 Woodure toddler tower stools can collapse or tip over, with openings a child's torso can pass through. Woodure reports 22 incidents and 15 injuries involving scrapes, cuts and bruises.

    Product
    Woodure Toddler Kitchen Step Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26656·2026-07-30

    Baby doll playsets recalled for choking hazard under federal small parts ban

    About 1,034 Mommy's Baby Lovely Deluxe Baby Doll Playsets sold on Temu contain small parts that pose a choking hazard to children under three. No injuries reported.

    Product
    Mommy's Baby Lovely Deluxe Baby Doll Playsets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26654·2026-07-30

    Sloosh dive sticks recalled for impalement risk under federal dive stick ban

    Joyin expanded its recall of Sloosh dive sticks to models 40003 and 16154 alongside model 40041. The sticks exceed the federal compression limit and pose an impalement hazard. No injuries reported.

    Product
    Sloosh Dive Sticks, models 40041, 40003 and 16154
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V499000·2026-07-30

    Brinkley RV Recalls 2027 Model I Trailers Due to Ladder Defect

    Brinkley RV is recalling 2027 Model I trailers because the exterior ladder may not be properly secured, posing a risk of injury if it detaches.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26646·2026-07-30

    KAIFAM 5-drawer dressers recalled for tip-over and entrapment hazards

    About 1,980 KAIFAM 5-drawer metal dressers sold on Amazon are unstable when not anchored to a wall and violate the STURDY Act standard. No injuries reported.

    Product
    KAIFAM 5-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V501000·2026-07-30

    Autocar Recalls 2023-2027 ACTT Tractors Due to ABS ECU Securing Issue

    Autocar is recalling 2023-2027 ACTT terminal tractors because the ABS Electronic Control Unit may be improperly secured, potentially causing system failure and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR E-ACTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26650·2026-07-30

    Movie souvenir cups and popcorn helmets recalled for button battery ingestion hazard

    About 55,350 Fantastic Four drinking cups and Captain America popcorn helmets with LED lights have accessible button cell batteries and lack the warning labels required by Reese's Law.

    Product
    Fantastic Four Drinking Cups and Captain America Popcorn Helmet Containers with LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0732-2026·2026-07-29

    Cetirizine Hydrochloride Tablets Recalled Due to Cross Contamination with Ranitidine

    JB Chemicals and Pharmaceuticals Ltd is recalling 34,020 bottles of Cetirizine Hydrochloride Tablets USP 5 mg because some tablets were found to contain Ranitidine due to cross contamination.

    Product
    CETIRIZINE HYDROCHLORIDE — CETIRIZINE HYDROCHLORIDE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0703-2026·2026-07-29

    Levothyroxine Sodium Tablets Recalled for Subpotency

    Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 88 mcg, lot N02310, due to subpotency. The recall is voluntary and affects nationwide distribution in the USA.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E051000·2026-07-29

    Toyota Recalls Side Curtain Air Bag Assemblies for Tundra Vehicles

    Toyota is recalling side curtain air bag assemblies for 2014-2021 Tundra vehicles because improper rolling may cause deployment issues, increasing injury risk.

    Product
    AIR BAGS:SIDE/WINDOW:CURTAIN recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0707-2026·2026-07-29

    Levothyroxine Sodium Tablets Recalled for Subpotency

    Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 25 mcg, due to subpotency. The recall affects nationwide U.S. distribution of specific lot numbers.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1178-2026·2026-07-29

    Dietary Supplement Modern Warrior Ready Recalled for Unapproved Ingredients

    Modern Warrior Life, LLC is recalling Modern Warrior Ready dietary supplements because they contain unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.

    Product
    Modern Warrior Ready, Dietary Supplement, 60 CAPSULES
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0700-2026·2026-07-29

    Levothyroxine Sodium Tablets Recalled for Subpotency

    Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets, 25 mcg, lot N02212, due to subpotency. The recall is nationwide and voluntary.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0705-2026·2026-07-29

    Levothyroxine Sodium Tablets Recalled for Subpotency

    Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium 125 mcg tablets (Lot N02266, Exp. 11/2026) nationwide due to subpotency, meaning the tablets may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0702-2026·2026-07-29

    Major Pharmaceuticals Recalls Levothyroxine Sodium Tablets Over Subpotency

    Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium Tablets, 75 mcg, NDC 0904-6951-61, due to subpotency. The recall affects lots N02172, N02296, and N02288 with expiration dates in July and December 2026, distributed nationwide.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide