The Recall Desk

State

Vermont product recalls

72,940 recalls have nationwide distribution and so reach Vermont. 1,983 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total
1,983
Critical
199
Severe
409
Most recent
2026-09-02

Of the 1,983 recalls naming Vermont we have scored against our rubric, 199 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 409 (21%) are Severe.

These figures cover only the 1,983 recalls whose distribution notice names Vermont specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4351–4375 of 74923

  • HighFDA (Devices)·Z-0482-2026·2025-11-19

    Electrosurgical snares recalled over small holes compromising package sterility

    Olympus is recalling 48,208 Single Use Electrosurgical Snares SD-400 because sterility may be compromised by small holes formed during packaging or transportation.

    Product
    Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use Electrosurgical Snare Model/Catalog Number: SD-400U-10 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and/or cauterization of di
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0475-2026·2025-11-19

    Maryland jaw sealers 23 cm recalled over residual material inside the device

    Medline is recalling 4,007 reprocessed LigaSure Maryland Jaw sealer/dividers, 23 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated, Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0471-2026·2025-11-19

    Five millimetre blunt tip sealers recalled over trapped residual material

    Medline is recalling two reprocessed LigaSure Blunt Tip sealer/dividers, 5 mm x 37 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal LigaSure Blunt Tip Sealer/Divider, Compatible with FT10 Generator, 5 mm x 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0477-2026·2025-11-19

    Maryland jaw sealers 44 cm recalled over trapped residual material

    Medline is recalling 9,547 reprocessed LigaSure Maryland Jaw sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0454-2026·2025-11-19

    CARESCAPE ONE monitors recalled over batteries that fail to hold charge

    GE Healthcare is recalling 5,935 CARESCAPE ONE patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.

    Product
    CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Updated 3/19 to add CARESCAPE ONE MBZ101 2087075-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0500-2026·2025-11-19

    Platelet reactivity tests recalled after an uncleared device was distributed

    Accriva Diagnostics is recalling 125 boxes, 3,125 tests, of VerifyNow PRUTest because a device without premarket clearance was incorrectly packaged and distributed.

    Product
    VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood test used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0466-2026·2025-11-19

    Radiography systems recalled over ceiling carriages that are hard to move

    Philips is recalling 284 Radiography 7300 C systems because some ceiling suspension telescopic carriages may be difficult to move vertically.

    Product
    Radiography 7300 C; Model Number: 712037;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0464-2026·2025-11-19

    DigitalDiagnost 4 systems recalled over ceiling carriages hard to move

    Philips is recalling 12 DigitalDiagnost 4 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.

    Product
    DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0484-2026·2025-11-19

    Laboratory cuvette arrays recalled over barcodes the analyser cannot read

    Becton Dickinson is recalling 29,760 BD Kiestra Isolate Suspension Cuvette Arrays because formatting errors in the 2D barcodes stop the analyser reading the expiration date.

    Product
    BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0465-2026·2025-11-19

    DigitalDiagnost C90 systems recalled over ceiling carriages resisting vertical movement

    Philips is recalling 223 DigitalDiagnost C90 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.

    Product
    DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0479-2026·2025-11-19

    ACL restoration implants recalled from one lot held in sales stock

    Miach Orthopaedics is recalling 167 BEAR Implants from a single lot, in an action the record says was limited to sales force trunk stock.

    Product
    BEAR Implant (Bridge-Enhanced ACL Restoration); Model/Catalog: 1000;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E078000·2025-11-18

    Mack Trucks Recalls Certain Vehicles Due to Electronic Control Unit Defect

    Mack Trucks is recalling certain vehicles because electrical noise may cause the electronic control unit to malfunction, potentially disabling safety systems like ABS and increasing crash risk.

    Product
    SERVICE BRAKES, AIR:ANTILOCK:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E077000·2025-11-18

    Volvo Trucks Recalls Bendix EC80 Electronic Control Units for Software Defect

    Volvo Trucks is recalling certain Bendix EC80 Advanced Electronic Control Units due to a software defect that may cause safety systems to fail, increasing crash risk.

    Product
    SERVICE BRAKES, AIR:ANTILOCK:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V798000·2025-11-18

    2024 Kawasaki Ninja ZX-6R Motorcycles Engine Stall Recall

    Kawasaki is recalling 2024–2026 Ninja ZX-6R motorcycles because a metal crankshaft bushing may seize, causing engine stall and increasing crash risk. Owners are advised not to ride until dealers re-tighten the bushing free of charge.

    Product
    KAWASAKI — KAWASAKI NINJA ZX-6R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V794000·2025-11-17

    Kia K5 fuel tank can expand and melt against hot exhaust

    Kia is recalling certain 2021-2024 K5 vehicles because a damaged check valve can let air into the fuel tank, causing it to expand, contact hot exhaust components and melt.

    Product
    KIA — KIA K5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V795000·2025-11-17

    Peterbilt 567 and 589 Trucks Recalled for Brake Air Tank Defect

    PACCAR is recalling 2026 Peterbilt 567 and 589 trucks because air tanks have insufficient volume, potentially reducing braking performance.

    Product
    PETERBILT — PETERBILT 589, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V797000·2025-11-17

    Hyundai IONIQ 5 front seat belt retractors may not be secured

    Hyundai is recalling certain 2025 IONIQ 5 vehicles because the seat belt retractors for the driver and front passenger seats may not be securely fastened.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V791000·2025-11-17

    Thor motorhome solar panel mounting brackets can loosen or break

    Thor Motor Coach is recalling certain 2022-2024 Tellaro, Sequence, Twist, Dazzle and other RVs because the solar panel mounting brackets may loosen or break, allowing the panel to detach.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TWIST, TRANQUILITY, DAZZLE, FREEDOM ELITE VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V796000·2025-11-17

    Hyundai Sonata fuel tank can expand and melt against hot exhaust

    Hyundai is recalling certain 2020-2023 Sonata vehicles because a damaged check valve can let air into the fuel tank, causing it to expand, contact hot exhaust components and melt.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V792000·2025-11-17

    Thor motorhome solar panel adhesive can fail allowing detachment

    Thor Motor Coach is recalling certain 2022-2024 Tellaro, Sequence, Dazzle, Scope, Rize and Twist RVs because the adhesive securing the solar panels to the roof may fail.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TWIST, TELLARO, DAZZLE, RIZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V793000·2025-11-17

    Ford E-350 and E-450 engine covers can become excessively hot

    Ford is recalling certain 2021 E-350 and E-450 vehicles that received an incomplete software update under recall 20V795, because the engine cover may become excessively hot.

    Product
    FORD — FORD E-350, E-450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V790000·2025-11-17

    Triple E Recalls 2025-2026 Unity RVs Due to Incorrect Seat Belt Labeling

    Triple E is recalling 2025-2026 Unity recreational vehicles because the weight label incorrectly lists a seating capacity of four, while the vehicle is equipped with only two seat belts.

    Product
    TRIPLE E — TRIPLE E UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide