The Recall Desk

State

Vermont product recalls

73,584 recalls have nationwide distribution and so reach Vermont. 2,011 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total
2,011
Critical
209
Severe
531
Most recent
2026-10-21

Of the 2,011 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 531 (26%) are Severe.

Which agencies issued them

These figures cover only the 2,011 recalls whose distribution notice names Vermont specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26276–26300 of 75595

  • SevereFDA (Devices)·Z-1237-2021·2021-03-17

    FDA Recalls CervAlign Anterior Cervical Plate System Due to Locking Mechanism Failure

    RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring surgical revision.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 5 Level, 105mm Material Number: 66-5105 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1213-2021·2021-03-17

    CervAlign Anterior Cervical Plate System Recalled for Locking Mechanism Failure

    RTI Surgical is recalling CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 28mm Material Number: 66-228 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1225-2021·2021-03-17

    RTI Surgical Recalls CervAlign Anterior Cervical Plate System

    RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 3Level, 57mm Material Number: 66-357 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1235-2021·2021-03-17

    RTI Surgical Recalls CervAlign Anterior Cervical Plate System Due to Locking Failure

    RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 88mm Material Number: 66-488 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1207-2021·2021-03-17

    RTI Surgical Recalls CervAlign Anterior Cervical Plate System Due to Locking Failure

    RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 16mm Material Number: 66-116 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1240-2021·2021-03-17

    FDA Recalls CervAlign Anterior Cervical Plate System Due to Locking Mechanism Failure

    RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 5 Level, 85mm Material Number: 66-585 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V186000·2021-03-17

    2021 Nissan Rogue Incorrect Wheel Nuts May Cause Wheel Separation

    Nissan is recalling certain 2021 Rogue vehicles with incorrect wheel nuts that may loosen and cause wheel vibration. This vibration may break wheel studs and cause wheel separation, increasing crash risk.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V184000·2021-03-17

    Jayco Travel Trailers Recalled for Potential Gas Leak Risk

    Jayco is recalling 2019-2020 travel trailers because a stove component may cause a gas leak, increasing fire risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK, JAY FEATHER, JAY FLIGHT SLX, JAY FLIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1179-2021·2021-03-17

    Draeger VentStar Watertrap Breathing Circuits Recalled for Detachment Risk

    Draeger Medical is recalling 150 units of VentStar Watertrap (N) 180 breathing circuits because the Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP00363 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1175-2021·2021-03-17

    Canon Medical System INFX-8000C C-Arm Recall for X-Ray Field Shift

    Canon Medical System is recalling 272 INFX-8000C C-arm systems nationwide because the x-ray irradiation field may shift relative to the displayed image at certain angles.

    Product
    System INFX-8000C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1180-2021·2021-03-17

    Dräger ID Circuit Basic Breathing Circuits Recalled for Detachment Risk

    Dräger Medical is recalling ID Circuit Basic (N) 180 breathing circuits because the Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP01327 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1182-2021·2021-03-17

    Sunstar G.U.M. Hydral Dry Mouth Spray Recalled for Bacterial Contamination

    Sunstar Americas is recalling 56,960 bottles of G.U.M. Hydral Dry Mouth Relief Oral Spray due to potential Burkholderia cepacia contamination.

    Product
    SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray, 2 FL.OZ. UPC0 70942 30713 0 - Product Usage: The device is formulated with water, moisturizers /humectants including one plant-based moisture rich humectant, sweeteners and flavors that collectively have lubricating…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1181-2021·2021-03-17

    Getinge Flow i Anesthesia Systems Recalled for Absorber Docking Failures

    Getinge Group Logistics America is recalling 144 Flow i Anesthesia Systems due to complaints of incorrect FiCO2 readings and System Check Out failures when docking the absorber.

    Product
    Anesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire ventilation of patients with no ability to breathe, as well as in supporting patients with limited ability to breathe.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0334-2021·2021-03-17

    Westminster Cracker Inc. Recalls Oyster Crackers Due to Plastic Foreign Object

    Westminster Cracker Inc. is recalling specific oyster cracker products because they may contain hard plastic foreign objects. Consumers should check their pantries for the affected items.

    Product
    Old Cape Cod Soup and Chowder Oyster Crackers - 8oz Box, 12 per case - UPC 093215801005; Westminster Bakers Co. Soup & Snack Crackers - 8oz Box, 12 per case - UPC 093215200426; Westminster Bakers Co. Soup & Snack Crackers - 8oz Box, 6 per case - UPC 093215200426
    Category
    Food
    Distribution
    13 states
  • HighCPSC·21097·2021-03-17

    HOFISH Recalls Mattresses for Federal Flammability Standard Violation

    HOFISH is recalling 10-inch hybrid mattresses sold on Amazon.com because they fail to meet the mandatory federal flammability standard, posing a fire hazard.

    Product
    HOFISH 10-Inch Hybrid Certi-PUR Certified Foam and Pocket Spring Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V185000·2021-03-17

    2021 Hyundai Santa Fe Air Bag Child Detection System Defect

    2021 Hyundai Santa Fe vehicles have a defective Occupant Detection System that may fail to prevent air bag deployment when a child restraint is detected in the front passenger seat, increasing crash injury risk.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1178-2021·2021-03-17

    Dräger VentStar Basic Breathing Circuits Recalled for Detachment Risk

    Draeger Medical is recalling 1,525 VentStar Basic breathing circuits because a Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    VentStar Basic (N) 180- Drager Breathing Circuits/Anesthesia Sets Order Number: MP00353 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1187-2021·2021-03-17

    Tosoh Thyroglobulin Antibody Calibrator Recalled for Calibration Failures

    Tosoh Bioscience Inc is recalling specific lots of Thyroglobulin Antibody Calibrators because some combinations with AIA PACKS resulted in unacceptable calibration values.

    Product
    Thyroglobulin Antibody (TgAB) Calibrator - Product Usage: intended for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of anti-thyroglobulin antibodies (TgAb) in human serum on specific TOSOH AIA System analyzers. Measurements obtained by this device aid in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2021·2021-03-17

    Physio-Control Recalls LIFEPAK CR2 Defibrillators Due to Missing Lid Magnets

    Physio-Control is recalling 89,763 LIFEPAK CR2 defibrillators because missing lid magnets may cause premature battery depletion.

    Product
    PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor use in a stationary environment. After the electrode pads are applied, the fully automatic model evaluates the heart rhythm and, if a shockable rhythm is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1188-2021·2021-03-17

    Siemens Dimension Vista HDLC Reagent Cartridges Recalled for Erroneous Results

    Siemens Healthcare Diagnostics is recalling Dimension Vista HDLC reagent cartridges due to discolored reagents that may cause erroneous test results.

    Product
    Dimension Vista HDLC - colorimetric method, lipoproteins - Product Usage: used as an aid in the diagnosis of lipid disorders (such as diabetes mellitus), various liver and renal diseases, and in the assessment of risk for atherosclerosis and cardiovascular disease.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1184-2021·2021-03-17

    MedComp Recalls Power Injectable CT Port Kits with Incorrect Port Size

    Medical Components, Inc. is recalling 96 Power Injectable CT Port kits because they contain 6.6F ports instead of the correct 5F size, which may prolong surgical procedures.

    Product
    Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated access to the vascular system.
    Category
    Medical Device
    Distribution
    Distributed nationwide