The Recall Desk

State

Vermont product recalls

73,104 recalls have nationwide distribution and so reach Vermont. 2,009 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total
2,009
Critical
209
Severe
419
Most recent
2026-09-23

Of the 2,009 recalls naming Vermont we have scored against our rubric, 209 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 419 (21%) are Severe.

These figures cover only the 2,009 recalls whose distribution notice names Vermont specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10676–10700 of 75113

  • HighFDA (Devices)·Z-2390-2024·2024-07-24

    Infusion Pump Set Recalled Due to Valve Malfunction Risk

    B. Braun's Infusomat UNIV. 60 infusion pump sets are recalled due to backcheck valve malfunction that may cause medication backflow from secondary to primary IV bags, risking adverse drug reactions or medication loss.

    Product
    Infusomat UNIV. 60 DROP PUMP SET, 2 CARESITES, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363423
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2373-2024·2024-07-24

    Horizon Bone Densitometer Devices Recalled for Electromagnetic Compatibility Issues

    Hologic Inc. is recalling 2,642 Horizon X-Ray Bone Densitometer units due to non-conformance with electromagnetic compatibility safety standards. The devices exceeded acceptable limits per international technical standard IEC 60601-1-2.

    Product
    Horizon X-Ray Bone Densitometer (DXA) Models: Horizon-A, Horizon-W, Horizon-WI, Horizon-C, Horizon-CI, Horizon-A-CN, Horizon-W-CN, Horizon-WI-CN, Horizon-CI-CN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1497-2024·2024-07-24

    FDA Recalls Black Coffee Beverages Due to Potential Under-Processing

    Snapchill, LLC is recalling approximately 549,146 cans of Black Coffee + Chocolate Syrup canned beverages marketed under Bold Bean Coffee Roasters and Larry's Coffee brands due to potential under-processing that may allow pathogenic growth.

    Product
    Black Coffee + Chocolate Syrup Canned Beverage packaged under the following brands and sizes: 1. Bold Bean Coffee Roasters The Chocolate One, 12 oz. UPC 8 10149-37108 0. 2. Larry's Coffee Nitro Mocha, 12 oz. UPC 8 50050-85512 5.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2395-2024·2024-07-24

    Infusomat SPACE Pump IV Set Recalled Due to Backcheck Valve Malfunction

    B. Braun Medical is recalling the Infusomat SPACE IV pump set (Model 480255) due to potential backcheck valve malfunction that could allow medication to flow backward between IV containers, potentially causing adverse drug reactions or loss of medication.

    Product
    Infusomat SPACE PUMP IV SET, 127 IN.-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 480255
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0611-2024·2024-07-24

    Potassium Chloride Extended Release Capsules Recalled for Dissolution Defect

    RemedyRepack Inc. is recalling Potassium Chloride Micro 10mEq K Extended Release Capsules because they fail to meet dissolution specifications, which could affect medication effectiveness.

    Product
    Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules, 30-count blister card, Rx only, MFG: Glenmark, Mahwah, NJ 07430, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-1203-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1511-2024·2024-07-24

    Canned Coffee Beverage Recalled for Potential Manufacturing Under-Processing

    Snapchill, LLC is recalling Fire Grounds Coffee Co. Vanilla Nito canned beverages due to potential under-processing. Approximately 549,146 cans were distributed nationwide in the United States and Canada.

    Product
    Coffee + Oat Milk + Vanilla Syrup Canned Beverage packaged under the following brands and sizes: 1. Fire Grounds Coffee Co. Vanilla Nito, 12 oz. UPC 8 50050-85504 0.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2361-2024·2024-07-24

    Abbott Proclaim 7 Implantable Pulse Generator May Reach End-of-Service Sooner Than Labeled

    Abbott is recalling 569 units of the Proclaim 7 implantable pulse generator because the device may reach end-of-service sooner than indicated in labeling. All affected units were distributed worldwide.

    Product
    Abbott Proclaim 7 Implantable Pulse Generator, REF 3663, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2363-2024·2024-07-24

    Abbott Proclaim 7 Pulse Generator Battery Life Shorter Than Labeled

    Abbott is recalling approximately 457 Proclaim 7 Implantable Pulse Generators because the battery may reach end of service sooner than indicated in labeling. Patients may require unexpected device replacement.

    Product
    Abbott Proclaim 7 Implantable Pulse Generator, REF 3667, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2404-2024·2024-07-24

    IV Infusion Pump Set Recalled for Backflow Risk During Medication Administration

    B. Braun Medical is recalling the OUTLOOK PUMP SET 3 IV infusion sets due to a potential backcheck valve malfunction that could cause medication to backflow from secondary containers into primary containers, risking adverse drug reactions and medication loss.

    Product
    OUTLOOK PUMP SET 3 CARESITE LADS 133 IN.-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number: 490564
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2406-2024·2024-07-24

    Surgical Hemostatic Device Recalled for Compromised Sterile Barrier

    Ethicon is recalling SURGICEL FIBRILLAR hemostatic pads due to torn foil pouches that compromise the sterile barrier, traced to a specific packaging machine defect.

    Product
    SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1961
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2367-2024·2024-07-24

    Abbott Proclaim DRG implantable pulse generator service life shorter than labeled

    Abbott is recalling 21,843 Proclaim DRG implantable pulse generators because the duration between the device's elective replacement indicator and end of service may be shorter than stated in product labeling.

    Product
    Abbott Proclaim DRG Implantable Pulse Generator, REF 3664, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2374-2024·2024-07-24

    BD Pyxis Automated Dispensing Cabinets Software Error Prevents Medication Access

    BD Pyxis automated dispensing cabinets with ES 1.7.x software may display errors preventing medication access when Component Manager is in 'installed mode' and patch KB 5033688 is applied.

    Product
    BD Pyxis: MedStation ES (Main), REF: 323; MedStation ES Tower, REF: 352; Anesthesia Station ES, REF: 327; CII Safe ES, REF: 1116-00; CII Safe ES, Desktop PC, Wired Scanner, REF: 107-254-01; CII Safe ES, Desktop PC, Wireless Scanner, REF: 107-255-01; CII Safe ES, Desktop…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0610-2024·2024-07-24

    OTC Oral Care Rinse Recalled Due to Microbial Contamination

    StellaLife VEGA Oral Care Peppermint rinse is recalled nationwide due to microbial contamination with Terribacillus species. The affected product was distributed to 60 physician offices.

    Product
    STELLALIFE VEGA ORAL CARE PEPPERMINT — STELLALIFE VEGA ORAL CARE PEPPERMINT (AZADIRACHTA INDICA, CALENDULA, ECHINACEA PURPUREA, PLANTAGO MAJOR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0607-2024·2024-07-24

    Prescription Potassium Chloride Extended-Release Capsules Recalled for Manufacturing Deviations

    Glenmark Pharmaceuticals is recalling Potassium Chloride Extended-Release Capsules nationwide due to manufacturing practice deviations. The voluntary recall affects multiple lot numbers, with no reported illnesses or injuries.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateNHTSA·24V555000·2024-07-24

    Thomas Built school bus emergency exit labels use lettering too small

    Daimler is recalling certain 2019-2022 Thomas Built school buses because the emergency exit label lettering is too small and may be difficult to read. 27,494 units affected.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, MINOTOUR DRW, SAF-T-LINER C2 JOULEY, MINOTOUR SRW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1503-2024·2024-07-24

    Emergency Medical Coffee Sweet Cream Canned Beverage Recalled for Potential Under-Processing

    Snapchill, LLC is recalling Emergency Medical Coffee Sweet Cream canned beverages due to potential under-processing. The recall affects 549,146 cans with expiration dates June 16, 2024–April 16, 2025, distributed nationwide in the US and Canada.

    Product
    Coffee + Non-Dairy Creamer + Sugar-Free Sweetener Canned Beverage packaged under the following brands and sizes: 1. Emergency Medical Coffee Sweet Cream, 12 oz. UPC 8 10149-37035 9.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V550000·2024-07-23

    Indian motorcycle rear suspension pushrods may buckle under load

    Indian Motorcycle is recalling certain 2024 Chieftain, Challenger, Pursuit, Roadmaster and Springfield motorcycles because the rear suspension pushrod may buckle under load.

    Product
    INDIAN — INDIAN ROADMASTER ELITE, SPRINGFIELD, ROADMASTER LIMITED, SPRINGFIELD DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V545000·2024-07-23

    Capacity Recalls 2023 TJ Series Vehicles Due to Steering Gear Defect

    Capacity of Texas is recalling 2023 TJ 5000, 6500, and 9000 vehicles because steering gear assemblies may have fewer recirculating balls than required, risking loss of steering control.

    Product
    CAPACITY — CAPACITY TJ 5000, TJ 9000, TJ 6500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V551000·2024-07-23

    Storyteller Overland Recalls 2024 GXV Next for Incorrect Load Label

    Storyteller Overland is recalling 2024 GXV Next vehicles because incorrect cargo capacity labels may allow overloading, increasing crash risk.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND GXV NEXT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·24V548000·2024-07-23

    Gulf States Toyota vehicles carry incorrect maximum capacity weight labels

    Gulf States Toyota is recalling a range of Toyota models because the maximum capacity weight value on the label is incorrect. 33,848 units are affected.

    Product
    TOYOTA — TOYOTA LAND CRUISER HYBRID, VENZA HYBRID, TUNDRA HYBRID, TACOMA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V546000·2024-07-22

    Motiv recalls electric chassis vehicles due to high-voltage software defect

    Motiv Power Systems is recalling 2019-2024 electric chassis vehicles because a software error may shut down high-voltage batteries, causing loss of power steering and braking.

    Product
    MOTIV — MOTIV F-53 BEV CHASSIS, F-59 BEV CHASSIS, E-450 BEV CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V547000·2024-07-22

    Motiv E-450 BEV Chassis Recalled for Wiring Damage Risk

    Motiv Power Systems is recalling 2021-2024 E-450 BEV chassis vehicles because damaged CAN signal wires could cause a loss of drive power, increasing crash risk.

    Product
    MOTIV — MOTIV E-450 BEV CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V544000·2024-07-19

    Doosan Portable Generator Trailer Recalled for Improperly Tightened Lug Nuts

    Doosan is recalling 2024 Bobcat PG25 portable generator trailers because improperly tightened wheel lug nuts may allow wheels to detach, increasing crash risk.

    Product
    DOOSAN PORTABLE POWER — DOOSAN PORTABLE POWER MOBILE GENERATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V543000·2024-07-19

    Blue Bird Recalls School Buses Due to Weak Roof Joints

    Blue Bird is recalling 2019-2023 Vision and All American school buses because roof joints may be too weak, risking panel separation in a crash.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, ALL AMERICAN, ALL AMERICAN SCHOOL BUS, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide