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.

651–675 of 76387

  • ModerateFDA (Devices)·Z-2743-2026·2026-07-22

    Photera 600 Phototherapy Device UV Sensor Calibration Error

    Daavlin Distributing Company is recalling 26 Photera 600 phototherapy devices nationwide because the UV sensor gain calibration is incorrect, causing inaccurate ultraviolet output readings.

    Product
    Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0687-2026·2026-07-22

    Meijer Earwax Removal Kit Recalled for Subpotent Active Ingredient

    Bell Pharmaceuticals is recalling Meijer Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotency: the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, limiting effectiveness.

    Product
    MEIJER EARWAX REMOVAL KIT — MEIJER EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2746-2026·2026-07-22

    Tosoh ST AIA-Pack Testosterone Diagnostic Test Kit Recall

    Tosoh Bioscience is recalling ST AIA-Pack Testosterone test kits due to low-quality control results that could produce falsely elevated or falsely low testosterone measurements, potentially leading to unnecessary testing or delayed diagnosis.

    Product
    ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers, Model Number 0025204
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0680-2026·2026-07-22

    Quality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall

    Bell Pharmaceuticals is recalling Quality Choice Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotent drug content, with assay levels significantly reduced (approximately 0.6% versus expected 6–7%) and low pH levels.

    Product
    QUALITY CHOICE EARWAX REMOVAL KIT — QUALITY CHOICE EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0688-2026·2026-07-22

    CAREone Earwax Removal Drops Recalled for Subpotent Active Ingredient

    CAREone Earwax Removal Drops (Carbamide Peroxide 6.5%) are recalled because the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, making it ineffective.

    Product
    CAREONE EARWAX REMOVAL DROPS — CAREONE EARWAX REMOVAL DROPS (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0682-2026·2026-07-22

    Audiologist's Choice Carbamide Peroxide Earwax Removal Recalls

    Bell Pharmaceuticals is recalling Audiologist's Choice Carbamide Peroxide earwax removal product due to subpotency: the active ingredient concentration is approximately 0.6% instead of the expected 6–7%, and the product has low pH.

    Product
    AUDIOLOGISTS CHOICE EARWAX REMOVAL SYSTEM — AUDIOLOGISTS CHOICE EARWAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0683-2026·2026-07-22

    Family Wellness Carbamide Peroxide Earwax Removal Kit Subpotent Drug

    Family Wellness Carbamide Peroxide 6.5% earwax removal kits are being recalled because they are subpotent with low pH and significantly reduced active ingredient content (approximately 0.6% versus the expected 6–7%). Consumers should stop using affected lots and consult their pharmacist.

    Product
    FAMILY WELLNESS EARWAX REMOVAL EARWAX AND BULB — FAMILY WELLNESS EARWAX REMOVAL EARWAX AND BULB (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2734-2026·2026-07-22

    Papablic Replacement Brush Heads Recalled Due to Breakage Risk

    Papablic Inc is recalling Papablic Replacement Brush Heads (Model PAPA317AA) due to potential for brush heads to break. The recall affects approximately 13,400 packs distributed nationwide.

    Product
    Papablic Replacement Brush Heads. Model Number: PAPA317AA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2736-2026·2026-07-22

    Medline Kits with Zimmer Biomet Mixing Bowls Recalled for Seal Defects

    Medline is recalling 163 kits containing Zimmer Biomet mixing bowls and spatulas due to seal nonconformities that may compromise sterility. The defect could require extended surgery time to locate an alternative device.

    Product
    Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2737-2026·2026-07-22

    Medline Kits with Zimmer Biomet Mixing Bowls and Spatulas Recalled

    Medline Industries is recalling 163 kits containing Zimmer Biomet mixing bowls and spatulas due to seal defects that risk sterility breach during surgical procedures.

    Product
    Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2740-2026·2026-07-22

    Rio II Nasal Pillows Interface Packaging and Labeling Discrepancy Recall

    3B Medical, Inc. is recalling Rio II Nasal Pillows Interface devices due to packaging and labeling discrepancies involving product size identification and device identifiers. The affected models are RII1001 (Small), RII1002 (Medium), and RII1003 (Large).

    Product
    Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number: RII1001 (Small), RII1002 (Medium), RII1003 (Large) Software Version: N/A Product Description: Nasal pillows interface intended for use with positive airway pressure therapy devices. The de
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V470000·2026-07-21

    Ford Recalls 2025-2027 Explorer and Lincoln Aviator for Seat Recline Issue

    Ford is recalling 76,748 2025-2027 Explorer and Lincoln Aviator vehicles because an unoccupied driver's seat may recline unintentionally, potentially trapping a second-row occupant.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·26V469000·2026-07-21

    Ember Recalls 2027 Travel Trailers Due to Incorrect VIN Labels

    Ember is recalling 2027 E-Series, Touring, and Overland travel trailers because the Federal Certification Label may list the wrong VIN, which could prevent owners from recognizing safety recalls.

    Product
    EMBER — EMBER E-SERIES, TOURING EDITION, OVERLAND SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V466000·2026-07-20

    Blue Bird Vision School Buses Recalled Due to Brake Line Fire and Crash Risk

    Blue Bird is recalling certain 2022-2027 Vision school buses because an exhaust hanger cotter pin may damage hydraulic brake lines, causing leaks that increase the risk of fire or crashes.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V467000·2026-07-20

    Blue Bird Recalls 2022-2027 Vision Transit Buses for Brake Line Damage

    Blue Bird is recalling 2022-2027 Vision transit buses because an exhaust hanger pin may damage the hydraulic brake line, causing leaks and increasing fire or crash risks.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V463000·2026-07-17

    Altec Recalls 2024-2026 AT Series Vehicles Due to Bearing Fastener Defect

    Altec is recalling 2024-2026 AT Series vehicles because turntable rotation bearing fasteners may not have been heat treated properly, posing a risk of component separation and injury.

    Product
    ALTEC — ALTEC AT SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V462000·2026-07-17

    Turtle Top Recalls 2026 Terra Ford Transit Buses Due to Lift Control Failure

    Turtle Top is recalling 2026 Terra Ford Transit buses because an electrical contactor may fail, preventing the wheelchair lift from stopping. This defect increases the risk of injury.

    Product
    TURTLE TOP — TURTLE TOP TERRA FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V465000·2026-07-17

    Great Dane Recalls 2027 Champion Trailers for Rear Impact Guard Defect

    Great Dane is recalling 2027 Champion dry van trailers because they may lack required rear impact guard extension channels, increasing injury risk in crashes.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26C004000·2026-07-17

    Evenflo Recalls Reo by Revolve360 Child Seats for Headrest Shift Risk

    Evenflo is recalling specific Reo by Revolve360 child seats because the headrest may shift during a crash, increasing injury risk.

    Product
    CHILD SEAT:SHELL:HEADREST:LOCKING MECHANISM recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V464000·2026-07-17

    Foretravel Recalls 2027 Realm Motorcoaches Due to Fire Risk

    Foretravel is recalling 2027 Realm Presidential Motorcoaches because a fan assembly circuit board may overheat, increasing the risk of a fire.

    Product
    FORETRAVEL — FORETRAVEL REALM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26621·2026-07-16

    Nottaway Chandelier Fixtures recalled for electrocution hazard risk

    Currey & Company is recalling about 447 Nottaway chandeliers due to lack of proper electrical grounding, which poses a risk of serious injury or death from electrocution. Consumers should stop using them immediately and contact the company for a free replacement.

    Product
    Nottaway Chandelier Fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26625·2026-07-16

    Madewell Women's Sweaters Recalled for Serious Burn Injury Risk

    Madewell is recalling about 5,900 Double V-Neck Pullover and V-Neck Cardigan sweaters because they violate mandatory clothing textile standards and pose a risk of serious burn injuries or death. The firm received one report of a sweater catching on fire, though no injuries have been reported.

    Product
    Madewell Double V-Neck Pullover and V-Neck Cardigan Sweaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26630·2026-07-16

    Adult Portable Bed Rails Recalled Due to Entrapment and Asphyxiation Risk

    MNIENT Adult Portable Bed Rails violate mandatory safety standards and pose risks of entrapment, asphyxiation, falls, and laceration. Consumers should stop using them immediately and contact the manufacturer for a refund.

    Product
    MNIENT Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26622·2026-07-16

    Wade Logan Annyka 9-Drawer Fabric Dressers Recalled for Tip-Over Risk

    About 180 Wade Logan Annyka 9-Drawer Fabric Dressers sold online at Wayfair.com from September 2023 through May 2026 are being recalled because they can tip over and pose entrapment hazards to children if not anchored to the wall.

    Product
    Wade Logan Annyka 9-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide