The Recall Desk

State

Montana product recalls

73,366 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.

Which agencies issued them

These figures cover only the 3,571 recalls whose distribution notice names Montana specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19151–19175 of 76937

  • HighFDA (Drugs)·D-0017-2023·2022-11-02

    Proton Armor Hand Sanitizer Recalled Due to Methanol Contamination

    Ultra Chem Labs Corp is recalling Proton Armor Anti-Microbial Alcohol-Free Foaming Hand Sanitizer nationwide due to trace amounts of methanol found in product components during manufacturing. The recall affects multiple bottle sizes with batch number 20117206.

    Product
    Proton Armor, Anti-Microbial Alcohol-Free Foaming Hand Sanitizer, kills 99.99% of germs, Green Tea and Aloe, Family Safe, No Gels, Water Based, 24 Hour Germ Protection with Moisturizers for Sensitive Skin, a) 8 oz bottle, b) 32 oz bottle, and c) 1.7 fl oz or 50 mL bottle…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0020-2023·2022-11-02

    Fondaparinux Sodium Injection Recalled Nationwide for Subpotent Formulation

    AuroMedics Pharma LLC is recalling 11,520 units of Fondaparinux Sodium Injection nationwide due to out-of-specification potency. Patients should contact their healthcare provider immediately.

    Product
    FONDAPARINUX SODIUM — FONDAPARINUX SODIUM (FONDAPARINUX SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0072-2023·2022-11-02

    Secrets of the Tribe Amla Alcohol-Free Extract recalled for elevated lead

    Secrets of the Tribe is recalling Amla Alcohol-Free Extract (2 oz and 4 oz bottles) distributed nationwide due to elevated lead levels.

    Product
    Amla Alcohol-Free Extract, 2 oz. glass bottle, UPC 041979376093 and Amla Alcohol-Free Extract, 4 oz. glass bottle, UPC 041979376116, Secrets of the Tribe LLC, PO Box 5264, Denver, CO, 80217
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0139-2023·2022-11-02

    Stryker INBONE Tibial Tray Recalled Due to Oversized Lock Detail

    Stryker INBONE Tibial Trays are being recalled due to an oversized lock detail that could affect proper component assembly and implant function. Affected units were distributed in New York.

    Product
    Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0137-2023·2022-11-02

    CorVocet Biopsy System recalled for needle ejection risk from component misalignment

    Merit Medical Systems is recalling CorVocet Biopsy Systems due to manufacturing defects that may cause the needle to eject when triggered outside the body, risking needle stick injuries to users or patients.

    Product
    CorVocet Biopsy System/Catalog Code: CORA1610/B, CORA1610S/B, CORA1615/B, CORA1810/A, CORA1810/B, CORA1810S/B, CORA1815/A, CORA1815/B, CORA1815S/A, CORA1815S/B, CORA1820/A, CORA1820/B, CORA1820S/A, CORA1825/A, CORA1825/B, CORA1825S/A, CORA2010/A, CORA2010/B, CORA2010S/A…
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-0125-2023·2022-11-02

    Hip Liner Implants Mixed with Knee Inserts in Packaging

    Encore Medical is recalling EMPOWR hip liner implants because boxes may contain knee inserts instead. This packaging error could delay surgeries. Four units affected in six US states.

    Product
    EMPOWR Acetabular System, Liner, 10 deg Hooded, HXe+ 40H, REF: 942-01-40H. Orthopedic implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0079-2023·2022-11-02

    The Chai Box Chai Concentrate Recalled for Botulinum Contamination

    The Chai Box Chai Concentrate is being recalled due to potential Clostridium botulinum contamination identified during testing. Affected products have best-by dates from September 2022 to March 2023.

    Product
    THE CHAI BOX CHAI CONCENTRATE UNSWEETENED 16FL OZ/473ML glass bottles UPC 7 93611 81925 2 REGRIGERATE AFTER OPENING. USE WITHIN 14 DAYS and 64FL OZ/1892ML plastic bottles KEEP REFRIGERATED USE WITHIN 7 DAYS OF OPENING UPC 7 93611 81926 9. INGREDIENTS Water, Black Teas, Spices…
    Category
    Food
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-0121-2023·2022-11-02

    Medline Peripheral Blood Culture Draw Kit Recall: Incorrect Expiration Dates

    Medline is recalling 1,020 peripheral blood culture draw kits due to incorrect expiration dates on kit components. The CHG solution and Bactec bottle plastic have expiration dates that do not match the date listed on the kit.

    Product
    MEDLINE PHERIPHERAL BLOOD CULTURE DRAW, Reorder #: DYNDH1561
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0120-2023·2022-11-02

    Medline Blood Culture Collection Kits Recalled for Incorrect Expiration Dates

    Medline recalls Adult Blood Culture Collection Kits due to incorrect expiration dates on kit components. The expiration dates on the CHG Solution and Bactec bottle plastic do not match the dates listed on the kit packaging.

    Product
    MEDLINE ADLT BLOOD CLUTURE COLLECT KIT, Reorder #: DYNDH1245
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0123-2023·2022-11-02

    Blood Culture Collection Kit Distributed with Mismatched Component Expiration Dates

    Medline is recalling 760 blood culture kits because the expiration dates printed on the kit do not match the expiration dates on the CHG Solution and Bactec bottle components inside.

    Product
    MEDLINE 24 BLOOD CLUTURE KIT, Reorder #: DYNDH1632
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0129-2023·2022-11-02

    ConvaTec Active Life Stoma Pouch Recalled for Release Liner Malfunction

    ConvaTec is recalling 3,209 units of its Active Life One-Piece Drainable Pouch due to impaired functionality of the release liner. Contact the manufacturer with your batch number.

    Product
    ConvaTec Active Life, One-Piece Drainable Pouch, 3/4-2 1/2 in., 19-64mm, REF 400598. For the management of stoma output following a colostomy or ileostomy procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0135-2023·2022-11-02

    LumiraDx SARS-CoV-2 Quality Control Kit: Incorrect Lot Numbers

    LumiraDx is recalling 83 SARS-CoV-2 Antigen Liquid Quality Control Kits (batch 2002204017) with incorrect vial lot numbers. The kits contain Flu A/B lot numbers instead of SARS-CoV-2 Ag numbers, causing error messages and preventing device use.

    Product
    LumiraDx SARS-CoV-2 Antigen (Ag) Liquid Quality Control Kit Catalog #: L016080109002 (EUA) The LumiraDx SARS-CoV-2 Quality Controls are intended for liquid quality control testing performed on the LumiraDx Instrument when used with the LumiraDx SARS-CoV-2 Ag Test Strip.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0126-2023·2022-11-02

    EMPOWER 3D Knee Tibial Insert Recall Due to Packaging Mix-Up

    Hip and knee implant boxes from Encore Medical may contain the wrong product, potentially causing surgery delays. The FDA is recalling affected units to prevent unavailability of correct implants.

    Product
    EMPOWER 3D Knee Tibial Insert, REF: 341-14-708. Orthopedic implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0132-2023·2022-11-02

    Vortex MP Port Titanium Recalled for Missing Printed Instructions

    Angiodynamics is recalling 11 Vortex MP Port Titanium implantable ports because printed Instructions for Use were not shipped with the devices. Missing instructions could lead to improper implantation or post-operative care.

    Product
    Vortex MP Port Titanium Low Profile Implanted Port with 5F attached Silicone Catheter and Tray. Indicated for central venous placement (either peripheral or chest placement) when patient therapy requires repeated venous access for injection or infusion therapy and/or venous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V817000·2022-11-01

    Brake modulator corrosion recall on Freightliner and Western Star commercial trucks

    Daimler Trucks North America is recalling certain Freightliner Cascadia and Western Star models due to corrosion in front brake modulator valves. The defect may cause brakes to pull to one side during automated braking, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, BUSINESS CLASS M2, 49X, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V818000·2022-11-01

    2017-2021 Tesla Model S and Model X power steering assist loss

    Tesla is recalling 2017-2021 Model S and Model X vehicles due to power steering assist failure on rough roads or after hitting potholes, which increases crash risk.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E092000·2022-11-01

    Tesla 2021 Model S Rearview Mirrors Recalled for Visibility Defect

    Tesla is recalling 2021 Model S exterior rearview mirrors that do not meet federal rear-visibility standards. Defective mirrors may cause drivers to misjudge vehicle distances, raising crash risk.

    Product
    TESLA — TESLA MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V816000·2022-10-31

    2021 Hyundai Santa Fe Hybrid seat belt pretensioners may explode in crash

    Hyundai is recalling 2021-2023 Santa Fe Hybrid and 2022-2023 Santa Fe Plug-In Hybrid vehicles, plus 2023 Genesis G80 Electric vehicles, because seat belt pretensioners may explode in a crash and project metal fragments. Dealers will secure the pretensioners with a cap at no cost.

    Product
    GENESIS — GENESIS, HYUNDAI G80 ELECTRIFIED, SANTA FE HYBRID, SANTA FE PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V813000·2022-10-31

    Forest River Recalls Fifth Wheels Due to Holding Tank Retention Defect

    Forest River is recalling specific 2019-2022 fifth wheels because a cross-member may fail to retain holding tanks, increasing crash risk.

    Product
    COACHMEN — COACHMEN, SHASTA CHAPARRAL, PHOENIX, BROOKSTONE, CHAPARRAL LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V815000·2022-10-31

    Volkswagen and Audi Vehicles Recalled for Tire Pressure Monitoring System Failure

    Volkswagen Group of America is recalling 296,044 Volkswagen and Audi vehicles (model years 2019-2021) because the tire pressure monitoring system may fail to detect simultaneous pressure loss in all four tires, increasing crash risk. Dealers will update the TPMS software at no charge.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI ATLAS CROSS SPORT, Q3, GOLF SPORTWAGEN, A3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V814000·2022-10-31

    Tiffin Motorhomes Recall Multiple 2022-2023 Models for LPG Hose Leak Fire Risk

    Tiffin is recalling approximately 295 motorhomes from 2022-2023 because the LPG hose fitting connected to the regulator may leak at the swivel joint, creating a fire hazard in the presence of an ignition source.

    Product
    TIFFIN — TIFFIN RED 360, ALLEGRO BAY, ALLEGRO BREEZE, PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V811000·2022-10-28

    Micro Bird Recalls G5 School Buses Due to Power Steering Defect

    Micro Bird is recalling 2019-2022 G5 school buses because a faulty connection may cause sudden loss of power steering and brake assist, increasing crash risk.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V812000·2022-10-28

    Micro Bird Recalls One 2019 G5 Transit Bus for Brake Fluid Leak

    Micro Bird is recalling one 2019 G5 transit bus because a faulty connection may cause power steering fluid loss, reducing brake assist and increasing crash risk.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·22T020000·2022-10-28

    Yokohama Recalls Tires with Incorrect Date Codes on Sidewalls

    Yokohama Off-Highway Tires America is recalling specific tires because the date code on the sidewall is incorrect, which hinders age identification.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide