The Recall Desk

State

Montana product recalls

73,576 recalls have nationwide distribution and so reach Montana. 3,572 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,572
Critical
689
Severe
952
Most recent
2026-10-14

Of the 3,572 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 3,572 recalls whose distribution notice names Montana specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

576–600 of 77148

  • HighFDA (Devices)·Z-3181-2026·2026-09-23

    Blood Culture Kits Recalled Due to Potential Sterile Barrier Compromise

    Medical Action Industries is recalling blood culture kits containing BD ChloraPrep applicators with potentially compromised sterile seals, posing a risk of localized skin infection.

    Product
    Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451; Blood Culture Kit 20/Cs, REF: 81834B; Blood Culture Collection Kit, REF: 81834C. All containing BD ChloraPrep Clear - 1 mL Applicators
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3191-2026·2026-09-23

    Datex-Ohmeda Aisys CS2 Anesthesia Systems Recalled for Gas Mixer Defect

    Datex-Ohmeda is recalling seven Aisys CS2 anesthesia systems because a gas mixer defect can interrupt anesthetic delivery, requiring clinician intervention to prevent decreased patient effect.

    Product
    Aisys CS2 with Et Control, Datex-Ohmeda anesthesia system, Part Number 1011-9000-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3210-2026·2026-09-23

    Medline Recalls Cataract Convenience Kits Due to Open Sterile Seals

    Medline Industries is recalling 336 cataract convenience kits because open sterile seals may compromise sterility and lead to patient infection.

    Product
    Convenience kits CATARACT PACK DYNJ59881A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V609000·2026-09-23

    Forest River Recalls 2026-2027 Dynamax Isata RVs Due to Ladder Defect

    Forest River is recalling 2026-2027 Dynamax Isata recreational vehicles because the bunk ladder may loosen if attached to a wooden mattress insert, increasing injury risk.

    Product
    DYNAMAX — DYNAMAX ISATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3184-2026·2026-09-23

    Stryker Recalls XCEL Bladeless Trocars Due to Cracking Risk

    Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.

    Product
    REF:B11LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 11X100MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0845-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product was distributed nationwide.

    Product
    Fluphenazine HCl Elixir, USP, 15 mg per 3 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3211-2026·2026-09-23

    Reign Medical Clench Staple System Recalled for Unestablished Performance

    F & A Foundation is recalling 600 units of Reign Medical Clench Staple Systems because the device's performance characteristics have not been adequately established.

    Product
    Reign Medical Clench Staple System (Compression), Description/REF: 9mm x 7mm/152-30907; 11mm x 10mm/152-31110; 15mm x 12mm/152-31512; 18mm x 18mm/152-31818; 20mm x 20mm/152-32020; 9mm x 7mm/152-40907; 11mm x 10mm/152-41110; 15mm x 12mm/152-41512; 18mm x…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3177-2026·2026-09-23

    Wilson-Cook Recalls Hemospray Endoscopic Hemostat Due to Adherence Issues

    Wilson-Cook Medical Inc. is recalling 121,241 units of Hemospray Endoscopic Hemostat due to issues with endoscope adherence and the inability to spray powder.

    Product
    Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7, HEMO-10, HEMO-7-EU, HEMO-10-EU Software Version: N/A Product Description: Hemostatic device for endoscopic gastrointestinal use Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3188-2026·2026-09-23

    Boston Scientific StoneSmart Connect Console Power Adapter Recall

    Boston Scientific is recalling StoneSmart Connect Console power adapters that may fail electrical safety testing due to high grounding resistance.

    Product
    Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1) DVI to HDMI Cable, (1) DisplayPort Cable REF: M0067933000, M006793300H0, M006793300R0, M006793300D0, M006793300Z0, M0067930000, M006793000R0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3172-2026·2026-09-23

    SunMed Tracheal Tube Recalled Due to Suction Catheter Passage Issues

    Well Lead Medical Co. Ltd is recalling SunMed Tracheal Tubes because a 6Fr suction catheter could not pass through the samples smoothly.

    Product
    SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0842-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product is distributed nationwide.

    Product
    Fluphenazine HCl Elixir, USP, 5 mg per 1 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3157-2026·2026-09-23

    ICU Medical Recalls IV Administration Sets with Drip Chamber Specks

    ICU Medical is recalling IV Non-Dedicated Gravity Administration Sets because black specks in the drip chamber may cause healthcare providers to delay therapy.

    Product
    IV Non-Dedicated Gravity Administration Sets with drip chambers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3180-2026·2026-09-23

    Embecta Medical Recalls Pen Needles Labeled for Investigational Use Only

    Embecta Medical II LLC is recalling pen needles labeled 'For Investigational Use Only' that were inadvertently distributed as commercially marketed devices.

    Product
    EWO_02513 (Catalog number 320122) For Investigational Use Only Nano Un-Cannulated Demo Samples Quantity 100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0844-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide.

    Product
    Fluphenazine HCl Elixir, USP, 10 mg per 2 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3158-2026·2026-09-23

    ICU Medical Recalls Oncology Sets with Drip Chamber Discoloration

    ICU Medical is recalling 107,800 oncology sets because drip chambers may contain black specks from the molding process, which could lead to product replacement and therapy delays.

    Product
    Oncology sets with drip chambers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0846-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product was distributed nationwide in the USA.

    Product
    Fluphenazine HCl Elixir, USP, 20 mg per 4 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3159-2026·2026-09-23

    ICU Medical Recalls Oncology Sets with Potential Drip Chamber Discoloration

    ICU Medical is recalling 28,550 oncology sets because drip chambers may contain black specks from the molding process. The discolored material does not enter the fluid path but may cause therapy delays.

    Product
    Oncology sets with drip chambers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0843-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide in the USA.

    Product
    Fluphenazine HCl Elixir, USP, 5 mg per 10 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0654-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0841-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product was distributed nationwide.

    Product
    Fluphenazine HCl Elixir, USP, 2.5 mg per 5 mL, Delivers: 5 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0654-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·022-2026·2026-09-22

    Star Meat Delivery Recalls Raw Pork, Beef, and Goat Products

    Star Meat Delivery Inc. is recalling raw pork, beef, and goat products produced without federal inspection and bearing false USDA marks.

    Product
    Star Meat Delivery Inc. Recalls Raw Pork, Beef, and Goat Products Produced Without the Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V604000·2026-09-22

    Nova Bus Recalls 2024-2025 LFS Transit Buses for Parking Brake Defect

    Nova Bus is recalling 2024-2025 LFS transit buses because an improperly tightened emergency brake valve may cause air leaks and unintentional parking brake activation.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E065000·2026-09-22

    Ford Recalls 2024-2026 Ranger Vehicles for Rearview Camera Display Failure

    Ford is recalling 2024-2026 Ranger vehicles with 10.1-inch center stack screens that may lose power and fail to display the rearview camera image, increasing crash risk.

    Product
    EQUIPMENT:ELECTRICAL:INFOTAINMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide