The Recall Desk

State

Montana product recalls

73,187 recalls have nationwide distribution and so reach Montana. 3,571 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,571
Critical
689
Severe
785
Most recent
2026-09-23

Of the 3,571 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 785 (22%) are Severe.

These figures cover only the 3,571 recalls whose distribution notice names Montana specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13451–13475 of 76758

  • HighFDA (Food)·F-0664-2024·2024-01-10

    Dietary supplement recalled due to potential mold contamination

    Spring Valley Biotin & Collagen Liquid is being recalled due to potential mold contamination. Approximately 24,324 units were distributed nationwide; consumers should stop using affected products.

    Product
    Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary Supplement 29 doses 1 fl oz (29mL) UPC: 194346065158 Packaged in a glass bottle in a paper carton
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0635-2024·2024-01-10

    EDS 3 CSF External Drainage System recalled for incomplete sterility testing

    Natus Medical is recalling 3,336 units of the EDS 3 CSF External Drainage System nationwide because incomplete bioburden testing cannot guarantee sterility. No illnesses have been reported, but non-sterile devices pose infection risk.

    Product
    EDS 3 CSF External Drainage System, REF: NT821731C, STERILEEO, Rx only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0628-2024·2024-01-10

    FDA Recalls Merit Pursue Microcatheter Due to Sterility Concerns

    Merit Medical Systems is recalling Merit Pursue Microcatheter devices distributed worldwide because sterility cannot be guaranteed. Patients should contact their healthcare provider.

    Product
    Merit Pursue Microcatheter, REF: 28HC17130SN, 28HC17150ST/A, 29HC2015045/A, 29HC20150SN/A, 29HC20150ST, CE 2797, STERILEEO, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0631-2024·2024-01-10

    Covidien Valleylab FT10 Energy Platform software issue causes inoperability

    Covidien is recalling Valleylab FT10 FT Series Energy Platform devices due to a software issue that may render new systems inoperable. The recall affects 47,901 units distributed worldwide.

    Product
    Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V011000·2024-01-10

    2022-2023 Lucid Air defrost heater failure reduces windshield visibility

    Lucid is recalling 2022-2023 Air vehicles whose high voltage coolant heater may fail to defrost the windshield, reducing visibility and increasing crash risk. Lucid will provide a software update and replace failed heaters at no cost.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0218-2024·2024-01-10

    Peritoneal Dialysis Solution Recalled for Lack of Sterility Assurance

    Fresenius Medical Care is recalling 69,590 bags of DELFLEX Peritoneal Dialysis Solution due to lack of sterility assurance. The affected lot was distributed nationwide.

    Product
    DELFLEX — DELFLEX (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V010000·2024-01-10

    2024 Volvo XC40 Left Rear Turn Signal May Not Function

    Certain 2024 Volvo XC40 vehicles may have a software error in the Central Electronic Module that disables the left rear turn signal indicator, increasing the risk of a crash if other drivers are not notified of turning.

    Product
    VOLVO — VOLVO XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0639-2024·2024-01-10

    Spinal fixation screws recalled due to incorrect size laser marking

    Zimmer Biomet Spine Inc. is recalling Vitality Polyaxial Screws (7.5mm x 50mm) due to incorrect laser marking showing 7.5 x 40. Incorrect screw size could cause perforation and vascular damage during spinal surgery.

    Product
    Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0623-2024·2024-01-10

    Medtronic Protege GPS Stent System Recalled for Packaging Seal Defects

    Medtronic is recalling Protege GPS Self-Expanding Peripheral Stent Systems due to seal defects in product packaging that could compromise sterility. Affected lot B644679 had national distribution.

    Product
    Protege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0629-2024·2024-01-10

    Microcatheter and Infusion Systems Recalled Due to Sterility Concerns

    Merit Medical Systems is recalling specific lots of microcatheter and infusion system devices because their sterility cannot be guaranteed. The devices were distributed worldwide including multiple US states and international locations.

    Product
    Fountain, REF: IS4-135-30 and IS4-90-10, CE2797, STERILEEO, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0634-2024·2024-01-10

    External Drainage System Collection Bags Recalled for Sterility Assurance Issues

    Natus Medical Incorporated is recalling 2,686 units of External Drainage System Collection Bags due to incomplete bioburden testing that prevents sterility assurance. Healthcare facilities and patients should contact the manufacturer or their healthcare provider for guidance.

    Product
    External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0213-2024·2024-01-10

    Prescription Oral Solution Eprontia Recalled for Out-of-Specification Impurity

    Azurity Pharmaceuticals recalls Eprontia (topiramate) oral solution nationwide because routine stability testing found an out-of-specification impurity. The chemical defect raised concerns about the drug's purity and patient safety.

    Product
    EPRONTIA — EPRONTIA (TOPIRAMATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0636-2024·2024-01-10

    Impella Connect medical device software portal disables unevaluated features

    Abiomed has disabled four features in the Impella Connect software portal because the FDA has not evaluated them for safety and effectiveness.

    Product
    Impella Connect, software portal for online device management that allows clinicians and Impella support staff to remotely view Impella data.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0625-2024·2024-01-10

    Reverse Shoulder Joint Implant System Recalled for Mislabeling

    Encore Medical is recalling 17 Reverse Shoulder System e+ surgical implants (Lot 381P1167) due to mislabeling. Affected units were distributed nationwide to multiple states.

    Product
    Reverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Constrained, Sterile H2o2, CE 2797
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0630-2024·2024-01-10

    KeySplint Hard Clear dental devices recalled for incorrect instructions

    Keystone Industries is recalling 336 units of KeySplint Hard Clear due to incorrect Instructions for Use packaged with the product. Affected units received KeySplint Soft instructions instead.

    Product
    KeySplint Hard Clear - Indicated for the fabrication of orthodontic and dental appliances such as mouthguards, nightguards, splints, repositioners, and retainers Item No.: 4220011
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0626-2024·2024-01-10

    Patella implant component recalled due to labeling error

    Encore Medical has voluntarily recalled a patella implant component (REF 130-03-738) due to mislabeling. The recall involves 2 units distributed nationwide.

    Product
    REF 130-03-738, All-Poly e + Patella, Domed Tri-Peg, 9x38mm, STERILE H2O2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V008000·2024-01-09

    PL Custom Recalls 2020-2024 Ambulances Due to Electrical Fire Risk

    PL Custom is recalling 2020-2024 Type 1 and Type 3 ambulances because a firmware defect may cause electrical circuits to overheat and catch fire.

    Product
    PL CUSTOM — PL CUSTOM TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V009000·2024-01-09

    Alexis Fire Equipment Recalls 2022-2023 Fire Trucks Due to Electrical Fire Risk

    Alexis Fire Equipment is recalling 56 fire trucks from 2022-2023 because a firmware defect may prevent electrical circuits from shutting off, increasing fire risk.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V006000·2024-01-08

    E-One Recalls Fire Trucks Due to Electrical Fire Risk

    E-One is recalling 408 fire trucks because a wiring defect may cause electrical circuits to overheat and start a fire.

    Product
    E-ONE — E-ONE TYPHOON N, COMMERCIAL, CYCLONE E, CYCLONE N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V007000·2024-01-08

    Marion Body Works Recalls 2024 Spartan Fire MetroStar Vehicles for Brake Defect

    Marion Body Works is recalling 2024 Spartan Fire MetroStar vehicles because a defective inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.

    Product
    MARION BODY WORKS — MARION BODY WORKS SPARTAN FIRE METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V005000·2024-01-08

    Coachmen Galleria motorhomes recalled for damaged wiring causing power steering loss

    Forest River is recalling Coachmen Galleria motorhomes (2020–2024) because battery boost wiring may become damaged, causing an electrical short circuit that results in loss of power steering, increasing crash risk.

    Product
    COACHMEN — COACHMEN GALLERIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V003000·2024-01-05

    Forest River Recalls 2020 Cherokee Travel Trailers Due to Draw Bar Defect

    Forest River is recalling 2020 Cherokee travel trailers because the draw bar locking mechanism may break, causing the trailer front to contact the road and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2024·2024-01-05

    Salm Partners Recalls Turkey Kielbasa Due to Bone Fragments

    Salm Partners, LLC is recalling ready-to-eat turkey kielbasa products due to possible contamination with bone fragments.

    Product
    Salm Partners, LLC — Salm Partners, LLC Recalls Ready-to-Eat Turkey Kielbasa Products Due to Possible Extraneous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V004000·2024-01-05

    Mickey Truck Bodies Recalls 37 Vehicles Due to Electrical Arcing Risk

    Mickey Truck Bodies is recalling 37 commercial trucks from 2020-2023 because exposed wiring on the refrigeration unit may cause electrical arcing and increase fire risk.

    Product
    MICKEY TRUCK BODIES — MICKEY TRUCK BODIES ISUZU NQR, CHEVROLET 5500 HD, HINO L6, CHEVROLET LCF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V002000·2024-01-04

    Terex Advance Concrete Mixer Trucks Recalled for Drum Separation Risk

    Terex Advance is recalling 2023-2024 concrete mixer trucks because bolts may loosen, causing the drum to separate from the vehicle.

    Product
    TEREX ADVANCE — TEREX ADVANCE CHARGER, COMMANDER, MM300
    Category
    Vehicle
    Distribution
    Distributed nationwide