The Recall Desk

State

Montana product recalls

20,084 recalls have nationwide distribution and so reach Montana. 0 additional recalls listed Montana specifically in their distribution scope.

About recalls in Montana

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Montana consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

6126–6150 of 20084

  • HighCPSC·25124·2025-02-06

    Ariens Snow Throwers Recalled Due to Laceration Hazard from Continued Rotation

    Ariens snow throwers may continue rotating after the operator releases the control lever, creating a laceration hazard. The company is offering free repairs at authorized dealers.

    Product
    Ariens® DELUXE-, PLATINUM- and PROFESSIONAL-series Snow Throwers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25118·2025-02-06

    TravisMathew Hoodies and Sweatshirts Recalled for Flammability Violation and Burn Hazard

    TravisMathew recalled approximately 59,450 women's and men's hoodies and sweatshirts sold from January through October 2024 due to violation of federal flammability standards, posing a burn hazard.

    Product
    TravisMathew Women's Sweatshirts and Women's and Men's Hoodies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V445000·2025-02-06

    Mercedes-Benz transmission wiring harness recalled for fire risk

    Mercedes-Benz USA is recalling certain 2019-2025 CLS 53, E 53, GT 43, and GT 53 models due to transmission wiring harness defects that may cause corrosion and electrical short-circuits, increasing fire risk. Dealers will replace the harness free of charge.

    Product
    MERCEDES-BENZ — 2023 MERCEDES-BENZ AMG GT53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V440000·2025-02-06

    2024 Ford Escape Adaptive Cruise Control Radar Misalignment

    Ford is recalling 2023-2024 Escape vehicles with adaptive cruise control due to misaligned radar modules. The misalignment can cause unexpected braking and loss of safety system function, increasing crash risk.

    Product
    FORD — 2024 FORD ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V445000·2025-02-06

    Mercedes-Benz Fuel Pump May Fail, Causing Loss of Drive Power

    Mercedes-Benz USA is recalling certain 2021–2023 vehicles with faulty fuel pumps that may shutdown and cause loss of drive power. Owners should contact dealers for free replacement.

    Product
    MERCEDES-BENZ — 2023 MERCEDES-BENZ AMG GT53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25128·2025-02-06

    Roll-Up Window Blinds Recalled for Child Strangulation and Entanglement Hazards

    Thy Trading Company recalls approximately 720 roll-up window blinds sold on Wayfair.com due to long operating cords that pose strangulation and entanglement hazards to children. Consumers should stop using the blinds immediately and request a full refund.

    Product
    Roll Up Window Blinds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V446000·2025-02-06

    2022–2023 Porsche 911 GT3 Rear Spoiler Control Software Error

    A software error in the rear spoiler control unit may cause brake lights to activate simultaneously on 2022–2023 Porsche 911 GT3 vehicles, potentially confusing other drivers.

    Product
    PORSCHE — 2022 PORSCHE 911 GT3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0211-2025·2025-02-05

    Prograf Tacrolimus Capsules Recall: Empty Capsules in Bottles

    Astellas Pharma recalls Prograf (tacrolimus) 0.5 mg capsules distributed nationwide due to empty capsules in bottles. Affected lot 0E3353D expires March 31, 2026.

    Product
    PROGRAF — PROGRAF (TACROLIMUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0991-2025·2025-02-05

    Medline Arterial Line Insertion Kits Recalled for Catheter Hub Defect

    Medline Industries is recalling 942 arterial line insertion kits due to excess material on the catheter hub of the catheter subassembly. The manufacturing defect prompted a FDA Class I recall of products distributed nationwide.

    Product
    Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT, Item Number ART1185B; 2) ARTERIAL LINE BUNDLE, Item Number ART255; 3) ARTERIAL LINE TRAY, Item Number ART350; 4) ARTERIAL LINE BUNDLE, Item Number ART355; 5) ARTERIAL LINE BUNDLE, Item Number ART355 ; 6)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0992-2025·2025-02-05

    Medline General Surgery Arterial Line Tray kits recalled for manufacturing defect

    Medline arterial line tray kits (models ART600 and ART690) are being recalled because the catheter hub contains excess material from manufacturing. The recall affects 58 kits distributed nationwide.

    Product
    Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY, Item Number ART600; 2) A LINE TRAY, Item Number ART690
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0210-2025·2025-02-05

    FDA Class I Recall: Astagraf XL Immunosuppressant Capsules May Be Empty

    Astellas Pharma is recalling Astagraf XL (tacrolimus) due to manufacturing defects; bottles shipped nationwide may contain empty capsules instead of medication.

    Product
    ASTAGRAF XL — ASTAGRAF XL (TACROLIMUS EXTENDED-RELEASE CAPSULES)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V335000·2025-02-05

    2025 Freightliner Business Class M2 park brake failure recall

    Daimler Trucks North America is recalling 2024-2025 Freightliner Business Class M2 vehicles because the park brake valve module may leak, causing park brake failure or unexpected engagement while driving.

    Product
    FREIGHTLINER — 2025 FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0431-2025·2025-02-05

    Frozen peach mango sorbet recalled for undeclared egg allergen

    The Mochi Ice Cream Company is recalling My Mochi Sorbet Peach Mango Sorbet nationwide due to undeclared egg allergen. Consumers with egg allergies should not consume this product.

    Product
    My Mochi Sorbet Peach Mango Sorbet; Keep Frozen; 6 pieces per container; 6-1.25 OZ (35g) PIECES NET WT 7.5 OZ (210g)*** Nutritional Panel: 6 servings per container; JOYFULLY CHILL!; Made in a nut-free facility; Made by My/Mochi, 5563 Alcoa Ave., Los Angeles, CA 90058; www.mymochi
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1058-2025·2025-02-05

    Karl Storz Uretero-Renoscope recalled for unapproved reprocessing instructions

    Karl Storz Endoskope Uretero-Renoscope (Model 27011L) is recalled due to Instructions for Use containing reprocessing procedures that have not been FDA-reviewed or approved. The recall affects 5 units distributed nationwide.

    Product
    KARL STORZ - ENDOSKOPE, REF: 27011L, Uretero-Renoscope, 8 Fr., 6¿, 43cm, NON STERILE, RxONLY, CE 0123
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1025-2025·2025-02-05

    AXIOS Stent Delivery System: Detaching Outer Sheath May Prevent Stent Expansion

    Boston Scientific is recalling 1,144 AXIOS Stent Delivery System units because the outer sheath's distal black tip can detach. If this occurs, the tip may remain around the stent saddle and prevent proper stent expansion, requiring device exchange.

    Product
    AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN: M00553650
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V376000·2025-02-05

    Travel trailers recalled for missing wardrobe cabinet backer board

    Certain 2021-2023 Keystone Arcadia travel trailers lack a backer board behind the wardrobe cabinet, potentially allowing the slide room to extend and cause injury. Dealers will install steel brackets to secure the slide room at no cost.

    Product
    KEYSTONE — 2021 KEYSTONE ARCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1020-2025·2025-02-05

    HemosIL Heparin Calibrators Recalled Over Quality Control Test Failures

    Instrumentation Laboratory recalls HemosIL Heparin Calibrators worldwide due to quality control failures. The diagnostic controls did not meet expected performance standards, potentially affecting accuracy of heparin testing in clinical laboratories.

    Product
    HemosIL Heparin Calibrators; Part Number: 0020300600; in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V287000·2025-02-05

    2025 Forest River Campsite Reserve travel trailers recalled for fire risk

    Forest River is recalling certain 2025 Campsite Reserve travel trailers because the solar controller may be wired incorrectly without over-current circuit protection, creating a fire risk.

    Product
    FOREST RIVER — 2025 FOREST RIVER CAMPSITE RESERVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V338000·2025-02-05

    2024 Kia EV9 Front Passenger Seat Belt Retractor May Fail

    Kia is recalling certain 2024 EV9 vehicles because the front passenger seat belt retractor cover may not be properly secured, which can prevent the seat belt from locking correctly during a crash.

    Product
    KIA — 2024 KIA EV9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1051-2025·2025-02-05

    Karl Storz Uretero-Renoscope Recalled for Unapproved Reprocessing Instructions

    Karl Storz is recalling a uretero-renoscope surgical device (REF 27003L) because the reprocessing instructions in the product documentation have not been reviewed or approved by the FDA.

    Product
    KARL STORZ - ENDOSKOPE, REF: 27003L, MICHEL Uretero-Renoscope, 9.5 Fr., 43cm, RxONLY, CE0123
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1067-2025·2025-02-05

    Implantable VNS Therapy Generators May Stop Delivering Treatment

    LivaNova is recalling approximately 8,223 SenTiva VNS Therapy generators due to a potential internal component failure that may cause the implanted device to stop delivering seizure therapy. Affected patients should contact their physician.

    Product
    Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva", Model 1000 Model/Catalog Number: 1000 Software Version: NA Product Description: The LivaNova VNS Therapy" System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy generator, lead, and exte
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1055-2025·2025-02-05

    Karl Storz Uretero-Renoscope recalled for unapproved reprocessing instructions

    Karl Storz Endoscopy has recalled the KARL STORZ ENDOSKOPE Uretero-Renoscope nationwide because its instructions for use contain reprocessing procedures that lack FDA review and approval for safety and efficacy.

    Product
    KARL STORZ - ENDOSKOPE, REF: 27010L, Uretero-Renoscope, 7 Fr., 43cm, NON STERILE, RxONLY, CE 0123
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1035-2025·2025-02-05

    Stent system outer sheath may detach, preventing proper expansion

    Boston Scientific's HOT AXIOS Stent has a reported defect where the outer sheath distal black tip can detach, preventing proper stent expansion and requiring device exchange.

    Product
    HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN: M00553550
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1060-2025·2025-02-05

    Karl Storz Ureteroscope Recall Due to Unapproved Reprocessing Instructions

    Karl Storz ureteroscopes are being recalled because their instructions contain reprocessing procedures that have not been reviewed or approved by the FDA. The recall affects 3,069 units distributed nationwide.

    Product
    KARL STORZ - ENDOSKOPE, REF: 27010K, Ureteroscope, 7 Fr., 34 cm, NON STERILE, RxONLY, CE 0123
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V253000·2025-02-05

    Mercedes-Benz C 300 and AMG C 43 Seat Belt Cover Defect Recall

    Mercedes-Benz is recalling certain 2022-2025 C 300 and 2023-2024 AMG C 43 vehicles. The driver-side seat belt cover may not be properly installed, potentially causing the seat belt anchor to loosen.

    Product
    MERCEDES-BENZ — 2022 MERCEDES-BENZ C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide