The Recall Desk

State

Montana product recalls

73,363 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
952
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 952 (27%) are Severe.

These figures cover only the 3,571 recalls whose distribution notice names Montana specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18951–18975 of 76934

  • ModerateNHTSA·22V883000·2022-11-29

    Winnebago Travel Trailers Recalled for Sharp Cabinet Door Handles

    Winnebago is recalling certain 2021-2022 travel trailers because cabinet door and drawer handles may have sharp edges. Dealers will replace the handles free of charge.

    Product
    WINNEBAGO — WINNEBAGO HIKE, MINNIE, MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22C007000·2022-11-28

    Marainbow Portable Infant Safe Seat Recall for Incorrect Installation Labels

    JD E-Commerce America Limited is recalling Marainbow Portable Infant Safe Seats because incorrect installation labels and design flaws prevent proper installation, increasing crash injury risk.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0066-2023·2022-11-23

    Hand Sanitizer Recalled for Methanol Contamination — FDA Class I

    Adam's Polishes ALCOHOL BASED HAND SANITIZER (multiple sizes) is recalled nationwide because FDA analysis found methanol contamination. This Class I recall poses a serious chemical health risk.

    Product
    Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b) 8 fl. oz (237 mL) spray bottle, NDC 74943-125-08; c) 1 PINT / 16 fl. oz (475 ml.) spray bottle, NDC 74943-125-16; and d) 1 GALLON / 128 fl.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V873000·2022-11-23

    2022 Chevrolet Silverado 1500 Air Bag System Defect Recall

    General Motors is recalling 5 2022 Chevrolet Silverado 1500 vehicles due to a manufacturing defect that left the air bag sensing diagnostic module in manufacturing mode. The module was not activated at the assembly plant, meaning air bags will not deploy in a crash.

    Product
    CHEVROLET — CHEVROLET SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V866000·2022-11-23

    2022 Dodge Charger Transmission Shifter Assembly Defect Recall

    Chrysler is recalling the 2022 Dodge Charger for shifter assembly defects. An improperly heat-treated shifter may slip out of drive position, causing sudden loss of power and increasing crash risk.

    Product
    DODGE — DODGE DURANGO, CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V871000·2022-11-23

    Marion Recalls 2021-2023 Spartan and KME Fire Trucks for Steering Defect

    Marion Body Works is recalling certain 2021-2023 Spartan and KME fire trucks because improperly heat-treated tie rod clamps may fail, causing loss of steering.

    Product
    SPARTAN FIRE — SPARTAN FIRE, KME GLADIATOR, METROSTAR, redundant PANTHER, FC-94
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0154-2023·2022-11-23

    Omnipod Dash PDM Insulin Pump Remote Recalled for Battery Fire Hazard

    Insulet Corporation is recalling the Omnipod Dash PDM remote controller for insulin pumps due to battery defects causing overheating, swelling, and fire hazard. A fire incident has been reported.

    Product
    18239: ASM Omnipod Dash PDM, insulin delivery system. PT-000010: Assembly, Dash Final PDM U100, mg/dL PT-000011: Assembly, Dash Final PDM U100, mmol/L PT-000030: Assembly, DASH PDM, Canada Remote Controller (Personal Diabetes Manager or PDM) associated with Insulin Pump…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V870000·2022-11-23

    2023 IC Bus Models Suspension and Steering Fastener Recall

    Navistar is recalling 2023 IC Bus EV, CE, and RE models due to improperly heat-treated fasteners in suspension and steering joints. These fasteners may lose tension and cause steering instability, increasing crash risk.

    Product
    IC BUS — IC BUS RESB, EV, CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V865000·2022-11-23

    Jeep Wrangler engine shutdown from loss of communication

    Certain 2021-2023 Jeep Wrangler 4xe vehicles may experience engine shutdown due to communication loss, reducing drive power and increasing crash risk.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V869000·2022-11-23

    International and IC Bus vehicles recalled for defective suspension and steering fasteners

    Navistar is recalling certain 2021-2023 International trucks and IC Bus vehicles because hex flange lock nuts in suspension and steering joints were improperly heat treated and may lose tension, creating a risk of steering instability.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS MV, TC, RESB, RE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V876000·2022-11-23

    2023 Thomas Built Buses SAF-T-LINER C2 Recalled for Battery Pack Defect

    Daimler Trucks North America is recalling 2023 Thomas Built Buses SAF-T-LINER C2 JOULEY school buses because an insufficient battery connection may cause sudden loss of drive power.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V875000·2022-11-23

    Nissan Recalls 2017 Rogue Vehicles Due to Wiring Fire Risk

    Nissan is recalling 2017 Rogue vehicles because water leaks can corrode a wiring connector, increasing the risk of a fire. Dealers will repair the issue free of charge.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0154-2023·2022-11-23

    Pedialyte Unflavored Electrolyte Solution Recalled for Seal Integrity Issues

    Abbott Laboratories is recalling Pedialyte Unflavored Electrolyte Solution 2 fl oz bottles due to compromised seal integrity that could lead to spoilage. The recall affects 14,588,544 bottles distributed in the US and internationally.

    Product
    Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case
    Category
    Drug
    Distribution
    50 states
  • HighNHTSA·22V874000·2022-11-23

    2021-2022 Chevrolet Heavy-Duty Trucks Recalled for Suspension Lock Nut Defect

    General Motors is recalling 2021-2022 Chevrolet 4500HD/5500HD/6500HD and XD models due to improperly heat-treated hex flange lock nuts in suspension and steering joints. The defective nuts may break, causing steering instability and increasing crash risk.

    Product
    CHEVROLET — CHEVROLET 4500HD, 5500XD, 4500XD, 6500HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0159-2023·2022-11-23

    Similac 360 Total Care Sensitive infant formula recalled due to compromised seal integrity

    Abbott Laboratories is recalling Similac 360 Total Care Sensitive infant formula due to compromised seal integrity that could lead to spoilage. Affected consumers should not use the product and contact Abbott for further instructions.

    Product
    Similac 360 Total Care Sensitive with Nipples 2 fl oz reclose able plastic bottle Packaged as: 4 - 6 count carton
    Category
    Food
    Distribution
    50 states
  • HighFDA (Devices)·Z-0232-2023·2022-11-23

    BD Phoenix diagnostic panel misformulated minocycline causes false resistance reporting

    BD Phoenix PMIC/ID-107 diagnostic panels contain misformulated minocycline that may produce false antibiotic resistance results, potentially delaying appropriate patient treatment.

    Product
    BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for the rapid identification and susceptibility of most aerobic and facultative anaerobic gram-positive bacteria of human origin with selected antimicrobial agents when used with the BD Phoenix Automated Microbiology…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V877000·2022-11-23

    Daimler Trucks Recalls 2023 FCCC MT50E Vans Due to Battery Defect

    Daimler Trucks North America is recalling 2023 FCCC MT50E vans because an insufficient battery connection may cause sudden loss of drive power, increasing crash risk.

    Product
    FCCC — FCCC MT50E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23711·2022-11-23

    Green Sprouts Stainless Steel Bottles and Cups Recalled for Lead Hazard

    Green Sprouts is recalling approximately 10,500 stainless steel straw bottles, sippy cups, and sip & straw cups because the bottom base can break off, exposing a solder dot containing lead. Children who ingest lead can suffer adverse health effects.

    Product
    Green Sprouts Stainless Steel Straw Bottles, Sippy Cups and Sip & Straw Cups
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0061-2023·2022-11-23

    Phenoxybenzamine Hydrochloride Capsules Recalled for Failed Specifications

    Par Pharmaceutical is recalling Phenoxybenzamine Hydrochloride Capsules 10mg nationwide due to failed impurity and degradation specifications. The recalled lot may not meet pharmaceutical quality standards.

    Product
    Phenoxybenzamine Hydrochloride Capsules, USP 10mg, 100-count bottles, RX only Dist. by: Par Pharmaceutical Chestnut Ridge, NY 10977 U.S.A. Mfg. by: Par Forumulations Private Limited,9/215, Pudupakkam, Kelambakkam - 603 103. NDC 49884-038-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0160-2023·2022-11-23

    Similac Neosure Infant Formula Recalled Due to Compromised Seal Integrity

    Abbott Laboratories is recalling Similac Neosure 2 fl oz bottles due to compromised seal integrity that could lead to spoilage. Approximately 14.5 million bottles distributed nationwide and internationally are affected.

    Product
    Similac Neosure 2 fl oz reclose able plastic bottle Packaged as: 48 count case
    Category
    Food
    Distribution
    50 states
  • HighFDA (Devices)·Z-0231-2023·2022-11-23

    Progressa hospital bed compression links may bend during head raising

    Baxter Healthcare is recalling 248 Progressa bed systems. Compression links may bend when raising the head section, even with patients under 500 pounds.

    Product
    Hill-Rom Progressa Bed System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0242-2023·2022-11-23

    Surgical Level 3 Gowns Recalled for Inadequate Fluid Protection

    Texas Medical Technology Inc. is recalling 100,000 Disposable Surgical Level 3 Gowns (sizes Large, XLarge, XXLarge) because the fabric fails to pass hydrostatic pressure tests, meaning blood and other body fluids may penetrate the gown.

    Product
    Disposable Surgical Level 3 Gown, Size/Product Code: Large/GWS-03-L-B, XLarge/GWS-03-XL-B, XXLarge/GWS-03-XXL-B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0230-2023·2022-11-23

    Spinal Decompression System Recalled for Potential Weld Breakage

    Boston Scientific is recalling 175 Superion Indirect Decompression System devices due to potential weld breakage at the spindle cap that may prevent proper deployment during implantation.

    Product
    Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0064-2023·2022-11-23

    FDA Recalls Labetalol Injectable for Potential Cross-Contamination Risk

    FDA recalls Nephron's Labetalol HCl Injection vials due to manufacturing deviations that could cause cross-contamination. The recall affects 34,020 vials distributed nationwide.

    Product
    PF-Labetalol HCl Injection, USP 20 mg/4 mL (5 mg/mL) vial, Rx Only, Nephron 503B Outsourcing Facility 4500 12th Street Extension West Columbia, SC 29172, NDC 69374-946-34, UPC 3 69374 94634 6.
    Category
    Drug
    Distribution
    Distributed nationwide