The Recall Desk

State

Montana product recalls

72,992 recalls have nationwide distribution and so reach Montana. 3,568 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,568
Critical
689
Severe
783
Most recent
2026-09-16

Of the 3,568 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 3,568 recalls whose distribution notice names Montana specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7976–8000 of 76560

  • HighFDA (Devices)·Z-1039-2025·2025-02-05

    Knee Implant Component Recalled for Incorrect Metal Post Assembly

    Zimmer, Inc. is recalling 155 units of NexGen LCCK Legacy knee implant components because the metal support post was assembled incorrectly in some units. The defective assembly could compromise implant function.

    Product
    NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1022-2025·2025-02-05

    Medtronic Percutaneous Reference Pins May Not Fit Properly

    Medtronic is recalling sterile percutaneous reference pins used in image-guided surgery because the pins may not fit into the patient reference frame or adapter, potentially affecting proper surgical tracking.

    Product
    Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The Sterile Percutaneous Reference Pin Set is intended to be used to place and remove a pin percutaneously into bony patient anatomy for rigid attachment of a pat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1061-2025·2025-02-05

    Karl Storz Ureteroscope recalled nationwide for unapproved reprocessing instructions

    Karl Storz Ureteroscope model 27000K is being recalled due to instructions for use containing reprocessing modalities not reviewed or approved by the FDA. The recall affects 82 units distributed nationwide.

    Product
    KARL STORZ - ENDOSKOPE, REF: 27000K, Ureteroscope, 7 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1036-2025·2025-02-05

    Medical stent delivery system outer sheath component detachment prevents proper expansion

    The HOT AXIOS Stent delivery system's outer sheath tip may detach during use, preventing proper stent expansion and requiring device exchange. Boston Scientific is recalling 1,102 units distributed nationwide.

    Product
    HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN: M00553560
    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
  • ModerateFDA (Devices)·Z-1063-2025·2025-02-05

    Karl Storz Ureteroscope Recalled for Unapproved Reprocessing Instructions

    Karl Storz is recalling 180 ureteroscopes due to instructions for use containing reprocessing procedures that have not been reviewed or approved by the FDA.

    Product
    KARL STORZ - ENDOSKOPE, REF: 27002K, Ureteroscope, 9.5 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1024-2025·2025-02-05

    AXIOS Stent Delivery System Outer Sheath May Detach During Deployment

    Boston Scientific's AXIOS Stent Delivery System is being recalled because the outer sheath can detach during use, preventing proper stent expansion and requiring device exchange.

    Product
    AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN: M00553640
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0209-2025·2025-02-05

    Badger 50 Mineral Sunscreen Recalled for Missing Drug Facts Labeling

    The W.S. Badger Company is recalling Badger 50 mineral sunscreen tins lacking the complete drug facts label, barcode, and directions for use. The recall affects 4,834 tins distributed nationwide.

    Product
    BADGER 50, ADVENTURE SPORT MINERAL SUNSCREEN WITH CLEAR ZINC, (uncoated 25% zinc oxide), 2.4 oz., Tin, W.S. Badger Company, Inc, 768 Route 10, Gilsum NH, 03448 UPC 6 34084 47150 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1042-2025·2025-02-05

    Medline procedure kits recalled for surgical mask bioburden contamination risk

    Medline procedure kits containing surgical masks are recalled nationwide because included masks failed to meet bioburden testing standards, creating potential infection risk during medical procedures.

    Product
    Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT, Reorder number DYNDC3189; dressing change tray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V054000·2025-02-04

    Highland Ridge Recalls 2025 Open Range 3X Trailers for Incorrect Tire Labeling

    Highland Ridge RV is recalling 2025 Open Range 3X fifth-wheel travel trailers because the vehicle certification label lists the wrong tire size, which could lead to incorrect tire installation.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW OPEN RANGE 3X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V052000·2025-02-03

    Temsa Recalls 2024 TS35 Vehicles Due to Fuel Hose Separation Risk

    Temsa is recalling 2024 TS35 vehicles with Cummins L9 engines because fuel filter hoses may separate, causing leaks, engine stalls, and fire or crash risks.

    Product
    TEMSA — TEMSA TS35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V053000·2025-02-03

    New Flyer Transit Buses Recalled for Fuel Hose Separation Risk

    New Flyer is recalling 210 transit buses because fuel filter hoses may separate, causing leaks, engine stalls, and fire risks.

    Product
    NEW FLYER — NEW FLYER XDE60, XD35, XD40, XD60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V051000·2025-01-31

    Roadtrek Recalls Westfalia Wave Vans Due to Incorrect Weight Labels

    Roadtrek is recalling 2023-2025 Westfalia Wave Pop Top vans because incorrect weight labels may lead to unintentional overloading and increased crash risk.

    Product
    ROADTREK — ROADTREK WESTFALIA WAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V048000·2025-01-31

    Ford and Lincoln rearview cameras may show blank or distorted images

    Ford is recalling certain 2021 Expedition, 2021-2022 Super Duty F-250 to F-600 and 2020-2022 Lincoln Corsair vehicles because the rearview camera may display a blank or distorted image.

    Product
    FORD — FORD, LINCOLN F-600 SD, F-450 SD, CORSAIR, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V049000·2025-01-31

    Ford Recalls 2025 Models for Instrument Panel Illumination Defect

    Ford is recalling 2025 Bronco Sport, Escape, and Lincoln Corsair vehicles because the instrument panel may fail to illuminate, increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR, ESCAPE, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V045000·2025-01-30

    Autocar Recalls 2023-2025 E-ACTT Vehicles Due to Software Error

    Autocar is recalling 2023-2025 E-ACTT vehicles because a software error may cause the vehicle to roll away on an incline or stall the engine.

    Product
    AUTOCAR — AUTOCAR E-ACTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25114·2025-01-30

    Portable Folding Stadium Seats Recalled Due to Fall and Injury Hazards

    AMX Global is recalling about 22,500 portable folding stadium seats because security hooks can crack and break, posing fall and injury risks. The company received reports of hook failures including falls and an injury.

    Product
    AMX Global Portable Folding Stadium Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25109·2025-01-30

    Matrix-brand Training Cycles Recalled Due to Unexpected Seat Collapse

    Johnson Health Tech North America is recalling approximately 12,885 Matrix-brand Training Cycles due to seats that can unexpectedly lower during use. The company received 63 reports, including two falls, but no injuries have been reported.

    Product
    Matrix-brand Training Cycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25113·2025-01-30

    Girls pajamas recalled due to flammability regulation violation, burn-injury risk

    Cozchique, Tebbis, and Beeziac girls pajamas sold on Amazon violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. About 6,050 units distributed May through September 2024.

    Product
    Cozchique, Tebbis and Beeziac Girls Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V043000·2025-01-30

    Jayco Recalls 2025 Jay Feather Micro Trailers Due to Gas Leak Risk

    Jayco is recalling 2025 Jay Feather Micro trailers because a cracked burner tube may cause a gas leak, increasing fire risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FEATHER MICRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V042000·2025-01-30

    Brinkley fifth wheel solar charge controllers can fail and overheat

    Brinkley RV is recalling certain 2024-2025 Model G fifth wheel trailers because the solar charge controller may fail and overheat, increasing the risk of fire.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL G
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25115·2025-01-30

    Pearhead Infant Learning Toy Sets Recalled for Choking Hazard in Rattle

    Pearhead Infant Learning Toy Sets are recalled because the wooden egg-shaped rattle can lodge in a child's throat, creating a choking hazard. The recall affects about 2,700 units sold from August through October 2024.

    Product
    Pearhead Infant Learning Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25112·2025-01-30

    Hair Dryers Recalled for Missing Immersion Protection, Electrocution Risk

    AliExpress is recalling about 980 Multi Styler Hair Dryers sold online from May 2023 through November 2024 because they lack an immersion protection device and pose an electrocution hazard if they fall into water while plugged in.

    Product
    6-in-1 Multi Styler and 5-in-1 Multi Styler Hair Dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25110·2025-01-30

    Cabinet Health 4 oz. Refillable Medicine Bottles Recalled for Degrading Lids

    Cabinet Health is recalling about 65,000 refillable 4 oz. medicine bottles. The plastic lids can degrade with repeated use, losing child-resistance and posing a poisoning risk if children access the contents.

    Product
    Cabinet Health 4 oz. Refillable Medicine Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide