The Recall Desk

State

Montana product recalls

72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6376–6400 of 76539

  • HighNHTSA·25V400000·2025-06-13

    Altec Recalls Aerial and Service Trucks Due to Electrical Defect

    Altec is recalling specific aerial and service trucks because a voltage spike may damage a control module, potentially causing a loss of vehicle control or brake performance.

    Product
    ALTEC — ALTEC L SERIES AERIAL DEVICE, SERVICE BODY, LS SERIES, TA CLASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V344000·2025-06-13

    Ford connecting rods and bearings may have manufacturing defects

    Ford is recalling certain 2025 Transit, F-150 and Explorer vehicles because connecting rod and rod bearing components may have manufacturing defects leading to engine failure.

    Product
    FORD — FORD EXPLORER, F-150, TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V390000·2025-06-12

    Chevrolet Silverado medium duty brake pressure switches may short and overheat

    GM is recalling certain 2019-2024 Chevrolet Silverado Medium Duty trucks because the brake pressure sensor may leak fluid into the switch and short circuit. Owners are told to park outside.

    Product
    CHEVROLET — CHEVROLET SILVERADO 4500, SILVERADO 6500, 6500, duplicate SILVERADO 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25337·2025-06-12

    Oliver & Smith 6-inch Mattresses Recalled for Fire Hazard Risk

    Agro Superior Group is recalling about 16,530 Oliver & Smith 6-inch mattresses sold online because they violate federal flammability standards and pose a risk of serious injury or death from fire. Consumers should stop using them immediately.

    Product
    Oliver & Smith 6-inch Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25339·2025-06-12

    Manual Retractable Pool Covers Recalled for Drowning and Entrapment Hazards

    Endless Pools is recalling about 11,500 Manual Retractable Security Pool Covers because improper installation can leave gaps larger than 4.5 inches, posing drowning and entrapment risks to children.

    Product
    Manual Retractable Security Pool Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25335·2025-06-12

    Skywalker Pro Via Ferrata Sets recalled due to fall-hazard risk

    Mammut Sports Group is recalling Skywalker Pro Via Ferrata Sets because the carabiner can open without engaging the safety latch, creating a risk of serious injury or death from falls.

    Product
    Skywalker Pro Via Ferrata Sets, Skywalker Pro Turn Via Ferrata Sets and Skywalker Pro Via Ferrata Packages
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25338·2025-06-12

    Anker PowerCore 10000 Power Banks Model A1263 Recalled for Fire and Burn Hazards

    Approximately 1,158,000 Anker PowerCore 10000 power banks (model A1263) are recalled because their lithium-ion batteries can overheat, creating fire and burn hazards. Anker has received 19 reports of fires and explosions, including property damage totaling over $60,700.

    Product
    Anker PowerCore 10000 power banks (model A1263 only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V391000·2025-06-12

    Honda and Acura brake pedal pivot pins may not be secured

    Honda is recalling certain Acura TLX, Acura MDX and Honda Pilot vehicles because the brake pedal pivot pin was not secured properly, which can shift the pedal out of position.

    Product
    ACURA — ACURA, HONDA TLX, MDX, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25336·2025-06-12

    Bugaboo Giraffe Highchairs Recalled for Fall Hazard Risk

    Bugaboo North America is recalling about 18,280 Giraffe highchairs because the legs can detach from the frame if screws are not properly tightened during assembly, posing a risk of serious injury or death. The company has received 22 reports of leg detachment, including 13 reports of minor injuries.

    Product
    Giraffe highchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·021-2025·2025-06-12

    Starway Recalls Ineligible Frozen Fish Balls Imported From Vietnam

    Starway International Group is recalling approximately 9,513 pounds of frozen fish balls imported from Vietnam because the producing establishment is not eligible to export to the US.

    Product
    Starway International Group LLC Recalls Ineligible Frozen Siluriformes Fish Ball Products Imported From Vietnam
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V392000·2025-06-12

    Volvo electric and hybrid models can lose braking in one-pedal mode

    Volvo is recalling certain electric and plug-in hybrid models because the vehicle may lose brake function while coasting downhill in "B" mode or One Pedal Drive. Owners are told not to use those modes until repaired.

    Product
    VOLVO — VOLVO XC60PHEV, XC90PHEV, XC40, EX40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25334·2025-06-12

    RYOBI 40V 24-Inch Cordless Hedge Trimmers Recalled for Laceration Hazard

    TI Outdoor Power Equipment is recalling about 113,000 RYOBI 40V 24-inch cordless hedge trimmers because the blade can unexpectedly activate from pressing only one control, causing lacerations. Consumers should stop using the trimmer and return it for a free replacement.

    Product
    RYOBI 40V 24-Inch Cordless Hedge Trimmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1814-2025·2025-06-11

    Adult Manual Resuscitator with Medium Adult Mask recalled nationwide

    SunMed Holdings is recalling 11,358 Adult Manual Resuscitators because the filter may be incorrectly attached to the patient port instead of the exhalation port, risking interruption or delay in patient resuscitation that could cause serious harm or death.

    Product
    Adult Manual Resuscitator with Medium Adult Mask, Bag REservoir, Filter, Manometer and 7 ft Oxygen Tubing, REF CPRM1116F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0456-2025·2025-06-11

    Fluoxetine Tablets 20 mg Recalled for N-Nitroso Impurity

    Torrent Pharma Inc. is recalling Fluoxetine Tablets, USP, 20 mg in a 28-count carton due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit.

    Product
    FLUOXETINE — FLUOXETINE (FLUOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1895-2025·2025-06-11

    Signature Laparoscopic Debakey Grasper Instruments Recalled for Insulation Defect

    Silex Medical is recalling 8 units of Signature Laparoscopic Debakey Grasper instruments (Model 5862100) due to incomplete insulation on the shaft near the rotator wheel, which could expose the user or patient to electrical contact.

    Product
    Signature Laparoscopic Instruments, Debakey Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862100.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1896-2025·2025-06-11

    Signature Laparoscopic Sharp Tooth Grasper Insulation Defect Recall

    Silex Medical recalls the Signature Laparoscopic Sharp Tooth Grasper due to incomplete insulation on the shaft near the rotator wheel, which creates an electrical hazard during use.

    Product
    Signature Laparoscopic Instruments, Sharp Tooth Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863020.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1887-2025·2025-06-11

    Palindrome Precision SI Chronic Hemodialysis Catheter Sterile Barrier Recall

    Mozarc Medical US LLC is recalling Palindrome Precision SI Chronic Hemodialysis Catheters (Sport Pack) due to a potential breach of sterile barrier packaging. Approximately 95,938 units distributed nationwide and in Canada and Mexico are affected.

    Product
    Palindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1899-2025·2025-06-11

    Signature Laparoscopic Atraumatic Grasper Instrument Insulation Defect Recall

    Silex Medical is recalling Signature Laparoscopic Atraumatic Grasper instruments (Model 5864000) due to incomplete insulation on the shaft that leaves an exposed area near the rotator wheel, posing an electrical safety risk during surgical use.

    Product
    Signature Laparoscopic Instruments, Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5864000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0455-2025·2025-06-11

    Fluoxetine Tablets USP 20 mg Recalled for N-Nitroso Contamination

    Torrent Pharma Inc. is recalling Fluoxetine Tablets USP 20 mg due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit. The affected lot is distributed nationwide.

    Product
    FLUOXETINE — FLUOXETINE (FLUOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1908-2025·2025-06-11

    Beckman Coulter Sample Probes with Defective Tips Clinical Chemistry

    Beckman Coulter is recalling sample probes with defective tips used in clinical chemistry analyzers. The defective probes may dispense lower sample concentrations, potentially leading to false low test results and delayed diagnosis.

    Product
    Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670
    Category
    Medical Device
    Distribution
    Distributed nationwide