The Recall Desk

State

Montana product recalls

73,190 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 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13626–13650 of 76761

  • HighNHTSA·23V871000·2023-12-21

    2023 Land Rover Range Rover Sport Exterior Lights May Fail

    Moisture may accumulate in the right-side tailgate and lights of certain 2023 Land Rover Range Rover Sport vehicles, causing exterior lights to fail and reducing visibility.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24068·2023-12-21

    TJX Foldable Wood and Rope Bistro Set Chairs Recall Due to Fall Hazard

    TJX is recalling about 29,000 foldable wood and rope bistro set chairs because the wooden frame can break or collapse when occupied, creating a fall hazard. The company has received eight reports of frame breakage, including six reports of minor injuries such as bruising and ankle strain.

    Product
    Foldable wood and rope bistro set chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0596-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nut Allergen

    Houdini Inc. recalls Acorn Raspberry Creme Filled Cookies from gift baskets for undeclared tree nuts. Approximately 4,875 cookies across 1,168 gift boxes were distributed nationwide. Consumers with tree nut allergies should not consume this product.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #926 Tis The Season Bakery Gift Box
    Category
    Food
    Distribution
    50 states
  • CriticalFDA (Food)·F-0592-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nut Allergen

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies found in gift baskets due to undeclared tree nuts. The cookies were distributed nationwide to all U.S. states.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #343 Brownie, Cookie & Cake Assortment
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0591-2024·2023-12-20

    Acorn Raspberry Cookies Recalled for Undeclared Tree Nut Allergen

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies sold in gift baskets due to undeclared tree nuts. Consumers with tree nut allergies should not consume the product.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #342 Bakery Bonanza
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0595-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nuts

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies found in gift basket #925 due to undeclared tree nuts. The product poses a health risk to consumers with tree nut allergies.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #925 Bakery, Coffee & Cocoa Gift Collection
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0597-2024·2023-12-20

    Acorn Raspberry Creme Filled Cookie Recall Due to Undeclared Tree Nuts

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies in gift basket #927 due to undeclared tree nut allergen. The cookies were distributed nationwide.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #927 Fresh Baked Cookie, Brownie and Cake Collection
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0590-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nuts

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies distributed nationwide in gift baskets due to undeclared tree nuts. Consumers with tree nut allergies face risk of allergic reaction.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #197 Gourmet Bakery Basket
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0589-2024·2023-12-20

    Cookie Gift Baskets Recalled for Undeclared Tree Nuts Allergen

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies in #067 Believe Cookie gift baskets (lot codes LC605975 and #106052023) due to undeclared tree nuts. Class I FDA recall; approximately 4,875 cookies nationwide.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0593-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nuts

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies in gift baskets due to undeclared tree nuts allergen. Consumers with tree nut allergies should not consume these products.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #359 Brownie, Cookie & Cake Sleigh
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Devices)·Z-0548-2024·2023-12-20

    CereLink ICP Extension Cable Recalled for Out of Range Readings

    Integra LifeSciences is recalling CereLink ICP Extension Cables due to a design defect causing out of range readings. The Class I recall affects 4,941 units distributed nationwide and internationally.

    Product
    CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP) Monitor, Model No. 826820/826820P. Cable is also provided with monitor as part of the same SKU.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0594-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nut Allergen

    Houdini Inc. is recalling 4,875 Acorn Raspberry Creme Filled Cookies from gift baskets due to undeclared tree nut allergen. These products were distributed across all U.S. states.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #373 Cookie, Brownie and Cake Winter Assortment
    Category
    Food
    Distribution
    50 states
  • HighFDA (Devices)·Z-0543-2024·2023-12-20

    Medical Diagnostic System Recall Due to Software-Related System Freezes and Delayed Results

    Ortho-Clinical Diagnostics is recalling the VITROS 3600 Immunodiagnostic System due to software issues causing system freezes and delayed test result reporting. The delays could affect patient care when rapid results are critical.

    Product
    VITROS 3600 Immunodiagnostic System Product Code 6802783 and Refurbished Product Code 6802914 Running Software Version 3.8.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0520-2024·2023-12-20

    Medical Device Recall: Para-Pak Zn-PVA Stool Collection Vials for Leakage Risk

    Meridian Bioscience is recalling Para-Pak Zn-PVA stool specimen collection vials due to a manufacturing defect that may cause leakage and risk exposure to biological hazards.

    Product
    Para-Pak Zn-PVA/10% Formalin-for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites Catalog Number: 301012
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0528-2024·2023-12-20

    Sterile PVP Medical Solution Recalled for Non-Sterile Contents

    Medline Industries is recalling 700 units of Sterile PVP solution because the labeling claims sterility but the contents are non-sterile. The affected products were distributed nationwide in eight states.

    Product
    STERILE PVP, REF DYNDA1649
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0519-2024·2023-12-20

    Para-Pak Clean Vial Stool Collection Kits Recalled for Manufacturing Defect

    Meridian Bioscience is recalling Para-Pak Clean Vials used for stool specimen collection due to a manufacturing defect that increases leakage risk and may expose users to biological hazards.

    Product
    Para-Pak Clean Vial-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: 900312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V864000·2023-12-20

    2022-2023 Toyota Corolla Cross air bag deployment defect recall

    Toyota is recalling 2022-2023 Corolla Cross vehicles where instrument panel defects may prevent the front-passenger air bag from deploying in a crash. Dealers will replace the panel at no cost.

    Product
    TOYOTA — TOYOTA COROLLA CROSS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0527-2024·2023-12-20

    Sterile Prep Stick Recall: Non-Sterile Contents Despite Sterile Labeling

    Medline Industries is recalling sterile prep sticks (REF DYNDA1134) labeled as sterile that contain non-sterile solution, posing infection risk in medical procedures.

    Product
    STERILE STERILE PREP STICK, REF DYNDA1134
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V865000·2023-12-20

    Toyota and Lexus vehicles recalled for air bag sensor short circuit defect

    Toyota and Lexus are recalling certain 2020-2022 vehicles with a faulty Occupant Classification System sensor that may prevent the front passenger air bag from deploying in a crash, increasing injury risk.

    Product
    LEXUS — LEXUS, TOYOTA ES, CAMRY HYBRID, AVALON, ES HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0523-2024·2023-12-20

    Collision Sensor Malfunction in Siemens ARTIS Icono Fluoroscopic X-Ray System

    The ARTIS icono fluoroscopic x-ray system may falsely detect collisions for up to 30 minutes after startup, requiring manual override with reduced safety protection and limiting diagnostic use.

    Product
    ARTIS icono (ceiling configuration), Fluoroscopic x-ray system; Model no. 11328100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0551-2024·2023-12-20

    Medical imaging software incorrectly displays patient studies to wrong patients

    Change Healthcare's Stratus Imaging PACS software can incorrectly associate patient imaging studies with the wrong patients. Approximately 454 affected units have been distributed nationwide.

    Product
    Change Healthcare Stratus Imaging PACS 1.4 and Stratus Imaging Share 1.4, a component of Stratus Imaging PACS.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0531-2024·2023-12-20

    Povidone Solution Labeled Sterile Despite Non-Sterile Contents

    Medline Industries recalls 300 units of Sterile Povidone (REF DYNDA2061) after discovering the solution inside foil sachets is non-sterile despite sterile labeling. Affected lots are distributed across eight states.

    Product
    STERILE POVIDONE, REF DYNDA2061
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V867000·2023-12-20

    Audi E-Tron Battery Modules May Overheat Creating Fire Risk

    Audi is recalling 2019-2022 E-Tron vehicles because high-voltage battery modules may overheat and increase fire risk. Dealers will install diagnostic software and replace affected modules at no cost.

    Product
    AUDI — AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0529-2024·2023-12-20

    Medline PVP Solution Recalled Due to Mislabeled Sterility

    Medline PVP Solution (REF DYNDA1858) is being recalled because it is labeled as sterile but contains non-sterile contents. 1,950 units are affected.

    Product
    PVP SOLUTION SING STRL, REF DYNDA1858
    Category
    Medical Device
    Distribution
    Distributed nationwide