The Recall Desk

State

Montana product recalls

73,509 recalls have nationwide distribution and so reach Montana. 3,572 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,572
Critical
689
Severe
952
Most recent
2026-10-14

Of the 3,572 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 952 (27%) are Severe.

Which agencies issued them

These figures cover only the 3,572 recalls whose distribution notice names Montana specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24601–24625 of 77081

  • LowFDA (Drugs)·D-0784-2021·2021-09-08

    Donepezil HCL Tablets 5 mg Recalled for Subpotency

    Jubilant Cadista Pharmaceuticals is recalling Donepezil HCL Tablets, USP, 5 mg (Lot # DN120006A, exp. 12/2021) because the tablets are subpotent—meaning they contain less active ingredient than specified. The recall affects 14,544 bottles distributed nationwide.

    Product
    Donepezil HCL Tablets, USP, 5 mg, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd. India, Marketed by: Jubilant Cadista Pharmaceuticals Inc. Salisbury, MD 21801 NDC 59746-329-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V694000·2021-09-07

    Eldorado EZRM Recalled for Fuel Hose Leak Fire Risk

    Eldorado National is recalling 2019-2021 EZRM vehicles with L9 Diesel Engines due to a fuel hose leak that increases fire risk.

    Product
    ELDORADO — ELDORADO EZRM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V693000·2021-09-07

    LDJ Recalls 2021 Thunder Creek Trailers Due to Fender Light Wiring Defect

    LDJ Manufacturing is recalling 279 2021 Thunder Creek trailers because improperly routed wiring may cause fender clearance lights to fail, increasing crash risk.

    Product
    THUNDER CREEK — THUNDER CREEK STT, MTO, SLT, MTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E084000·2021-09-04

    Nineo F2-H11 LED Bulbs Recalled for Excessive Brightness

    Nineo is recalling F2-H11 replacement LED bulbs because they may be too bright, posing a glare hazard to oncoming drivers.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V691000·2021-09-03

    2021 Forest River Berkshire RVs Recalled for Electrical Fire Risk

    Forest River is recalling certain 2021 Berkshire recreational vehicles that may have unsealed mini-breakers in the electrical system, which could cause sparks and increase the risk of fire in the battery compartment.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V692000·2021-09-03

    2021-2022 Coachmen Nova motorhomes recalled for improper battery installation

    Forest River is recalling 2021-2022 Coachmen Nova motorhomes because the Absorbed Glass Mat battery was incorrectly installed, allowing hydrogen gas to accumulate inside the vehicle and create a risk of injury.

    Product
    COACHMEN — COACHMEN NOVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V686000·2021-09-02

    Highland Ridge RV Recalls 1,157 Units Due to Propane Regulator Failure

    Highland Ridge RV is recalling 1,157 recreational vehicles because a propane regulator may fail, causing increased pressure and fire risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW OPEN RANGE, OPEN RANGE ULTRA LITE, OPEN RANGE LIGHT, SILVERSTAR LIMITED
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V688000·2021-09-02

    Toyota Tundra vehicles recalled due to headlight electrical circuit fire risk

    Certain 2018-2021 Toyota Tundra vehicles have a headlight electrical circuit defect that may power high and low beams simultaneously, causing connector overheating and fire risk. Owners should contact Toyota or NHTSA for remedy information.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21778·2021-09-02

    Step2 StepUp Sidekick Learning Towers Recalled Due to Fall Hazard

    The Step2 Company is recalling StepUp Sidekick Learning Towers because the storage tray with cup holders and step can come loose, posing a fall hazard to children. Step2 has received 20 reports of the component coming loose, including one report of minor bruises from a fall.

    Product
    StepUp Sidekick Learning Towers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V689000·2021-09-02

    Freightliner Cascadia trucks recalled for potential steering linkage separation

    Daimler Trucks North America is recalling 2019-2021 Freightliner Cascadia trucks due to improperly tightened drag link taper joints that could separate from the steering arm. Loss of steering control could result, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V681000·2021-09-02

    Indian Recalls 2020 Scout Bobber Sixty for Inoperable Brake Lights

    Indian Motorcycle is recalling 2020 Scout Bobber Sixty models because an ECU update may have disabled brake lights, increasing crash risk.

    Product
    INDIAN — INDIAN SCOUT BOBBER SIXTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V687000·2021-09-02

    2021 Starcraft Telluride RV Propane Regulator Failure Fire Risk

    Starcraft is recalling certain 2021-2022 recreational vehicles with defective Winntec propane regulators that may fail, causing increased pressure and larger flames in gas appliances, raising fire risk.

    Product
    STARCRAFT RV FW — STARCRAFT RV FW, STARCRAFT RV TT TELLURIDE, SUPER LITE, AUTUMN RIDGE OUTFITTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V685000·2021-09-02

    Jayco Recreational Vehicles Recalled for Propane Regulator Fire Risk

    Jayco is recalling certain 2017-2022 recreational vehicles with Winntec propane regulators that may fail and increase propane pressure, raising the risk of fire in gas appliances.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER, JAYCO SEISMIC, JAY FEATHER, EAGLE, redundant SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2285-2021·2021-09-01

    Monoject Sodium Chloride Flush Syringes Recalled for Air Embolism Risk

    Cardinal Health recalls 267 million Monoject 0.9% Sodium Chloride Flush Syringes due to a plunger defect that may reintroduce air into the syringe, posing a risk of air embolism during IV administration.

    Product
    Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0765-2021·2021-09-01

    Fludarabine Phosphate Injection Recalled Due to Sterility Concern

    Custopharm, Inc. is recalling Fludarabine Phosphate for Injection, USP 50 mg because the manufacturer detected microbial contamination during environmental monitoring in aseptic manufacturing areas, raising sterility assurance concerns.

    Product
    FLUDARABINE PHOSPHATE FOR INJECTION, USP, 50 mg per vial, Single dose vial, Rx Only, Mfd for: Leucadia Pharmaceuticals Carlsbad, CA 92011 U.S.A, NDC 24201-237-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2286-2021·2021-09-01

    Sodium Chloride Flush Syringe Recalled Due to Plunger Malfunction Risk

    Cardinal Health is recalling Monoject 0.9% Sodium Chloride Flush Syringes because the plunger may draw back after use and reintroduce air into the syringe.

    Product
    Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0768-2021·2021-09-01

    SterRx Sodium Bicarbonate in 5% Dextrose Injection Recalled for Sterility Concerns

    SterRx is recalling Sodium Bicarbonate in 5% Dextrose Injection (1,000 mL bags) nationwide due to lack of assurance of sterility. Patients using affected lots should consult their healthcare provider immediately.

    Product
    Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL bags, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0767-2021·2021-09-01

    SterRx Sodium Bicarbonate Injection Recalled for Non-Sterility

    SterRx is recalling Sodium Bicarbonate in 5% Dextrose Injection due to microbial contamination confirmed by third-party laboratory testing. The affected product is a prescription intravenous injection distributed nationwide.

    Product
    Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL bags, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903 NDC 70324-326-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V684000·2021-09-01

    Mack Recalls 2020-2022 MD Trucks Due to Brake Pedal Defect

    Mack is recalling 2020-2022 MD trucks because a defective cotter pin may leave the brake pedal unsecured, increasing crash risk.

    Product
    MACK — MACK MD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2284-2021·2021-09-01

    Monoject flush syringe recall: plunger may reintroduce air into IV lines

    Cardinal Health Monoject flush syringes may have a defect allowing the plunger to draw back and reintroduce air into the syringe. The FDA issued a Class I recall for over 267 million units distributed nationwide.

    Product
    Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0773-2021·2021-09-01

    Trulicity autoinjector pens recalled for incorrect strength labeling

    Eli Lilly & Company is recalling Trulicity (dulaglutide) 0.75 mg autoinjector pens because some contain double the labeled strength. Affected patients may receive an incorrect dose.

    Product
    TRULICITY — TRULICITY (DULAGLUTIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0772-2021·2021-09-01

    Atovaquone Oral Suspension Recalled for Temperature Abuse

    KVK-Tech, Inc. is recalling Atovaquone Oral Suspension due to temperature abuse that caused unusual grittiness in the product. The defect may affect the medication's quality and safety.

    Product
    ATOVAQUONE ORAL SUSPENSION — ATOVAQUONE ORAL SUSPENSION (ATOVAQUONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0880-2021·2021-09-01

    Cahills Ireland Whiskey Cheese recalled for Listeria monocytogenes contamination

    Cahills Farm Cheese Limited is recalling Cahills Ireland Whiskey Cheese 5lb. Waxed Deli Wheels due to potential Listeria monocytogenes contamination. The affected product was distributed nationwide.

    Product
    Cahills Ireland Whiskey Cheese - 5lb. Waxed Deli Wheel
    Category
    Food
    Distribution
    Distributed nationwide