The Recall Desk

State

Vermont product recalls

72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7451–7475 of 74967

  • HighNHTSA·25V153000·2025-03-11

    Nissan Sentra driver seat frames may not be fully secured

    Nissan is recalling certain 2025 Sentra vehicles because the driver's seat frame may not be fully secured to the outer side of the seat track, failing FMVSS 207 and 210.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V150000·2025-03-07

    Mercedes-Benz Recalls 2023 EQE Models for Detaching Wheel Rim Inserts

    Mercedes-Benz is recalling 2023 EQE 350 4MATIC and EQE 350+ vehicles because wheel rim inserts may detach while driving, creating a crash hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQE 350+, redundant EQE 350 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V149000·2025-03-07

    2025 Forest River Aurora Travel Trailers Electrical Fire Risk Recall

    Forest River is recalling certain 2025 Aurora ART26BHS travel trailers because the air conditioner electrical connector may have exposed wiring strands that can cause electrical arcing and fire.

    Product
    FOREST RIVER — FOREST RIVER AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25160·2025-03-06

    Nuby Stroller Fans recalled due to laceration injury hazard

    Nuby Stroller Fans are recalled because the housing allows children's fingers to contact the spinning blade, causing lacerations; six injuries have been reported. Consumers should stop using the product immediately and contact the manufacturer for a free replacement.

    Product
    Nuby Stroller Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25168·2025-03-06

    Children's Nightgowns and Robes Recalled for Flammability and Burn Hazard

    Marie-Chantal children's nightgowns, pajama sets and robes violate federal flammability standards for sleepwear, posing a risk of serious burn injuries. About 560 units sold nationwide from November 2021 through October 2024; consumers should stop use immediately.

    Product
    Marie-Chantal Children's Nightgowns, Pajama Sets and Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25172·2025-03-06

    Love Our Home Crib Bumpers Recalled for Federal Ban Violation and Suffocation Risk

    Love Our Home braided crib bumpers sold on Shein.com violate the federal Safe Sleep for Babies Act and pose a suffocation hazard to infants. About 750 units were sold between March and November 2024.

    Product
    Love Our Home Braided Crib Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25170·2025-03-06

    Auto World Unassembled Slot Cars Recalled for Loose Magnet Ingestion Hazard

    About 55,000 Auto World Unassembled Deluxe Pit Kit Slot Cars are being recalled because loose magnets in unassembled kits pose an ingestion hazard to children. The products were sold nationwide from July 2023 to February 2024.

    Product
    Auto World Unassembled Deluxe Pit Kit Slot Cars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V145000·2025-03-06

    Jayco Recalls 2024-2025 Motorhomes Due to Incorrect Federal Load Labels

    Jayco is recalling specific 2024 and 2025 motorhomes because incorrect Federal labels may allow the vehicles to be overloaded, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO CONDOR, ALANTE SE, REDHAWK SE, ODYSSEY SE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V147000·2025-03-06

    2024 INEOS GRENADIER door latch assembly defect recall

    INEOS is recalling certain 2024 Grenadier vehicles because the door button mechanism may lack sufficient grease, preventing the door from fully latching. An unlatched door can open unexpectedly while driving, increasing injury risk.

    Product
    INEOS — INEOS GRENADIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V146000·2025-03-06

    2024 Kawasaki Z500 and Ninja 500 Motorcycles Clutch Release Shaft

    Kawasaki is recalling certain 2024 Z500 and Ninja 500 motorcycles due to improper welding of the clutch release shaft, which can cause the clutch lever to break and disable the motorcycle, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI Z500, NINJA 500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V148000·2025-03-06

    Cadillac CT5 and related vehicles transmission lock-up recall

    General Motors is recalling certain 2019–2022 Cadillac and Chevrolet vehicles with 10-speed transmissions due to internal transmission damage that may cause wheel lock-up while driving.

    Product
    CADILLAC — CADILLAC, CHEVROLET CT4, CT6, CT5, CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25173·2025-03-06

    Taylor Water Technologies Recalls Phosphate Reagent Bottles Due to Chemical Burn Risk

    Taylor Water Technologies is recalling about 10,000 Phosphate Reagent #1 bottles sold with test kits. The sulfuric acid bottles lack required child-resistant packaging, posing a risk of severe chemical burns.

    Product
    Phosphate Reagent #1 Bottles sold within the Taylor Phosphate Test Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25167·2025-03-06

    BD Recon LT Avalanche Transceivers Recalled Due to Switch Corrosion

    BD Recon LT avalanche transceivers are recalled because the switch mechanism can corrode and fail, potentially preventing rescuers from locating avalanche victims. Six devices have malfunctioned; no injuries reported.

    Product
    BD Recon LT Avalanche Transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0578-2025·2025-03-05

    Gerber Baby Teething Sticks Recalled Due to Choking Risk

    Nestlé-USA is recalling all lots of Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Strawberry Apple flavor following complaints of infant choking. The product was distributed across 42 states and Puerto Rico.

    Product
    Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER PRODUCTS CO., FREMONT, MI 49413
    Category
    Food
    Distribution
    46 states
  • SevereFDA (Food)·F-0579-2025·2025-03-05

    Gerber Baby Soothe 'n' Chew Teething Sticks Recalled for Choking Risk

    Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Banana flavor are recalled nationwide due to complaints of infant choking. All lots in both 1.59 oz and 3.2 oz packages are affected.

    Product
    Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2 OZ (90g) box UPC 0 15000 04608 8 and NET WT 1.59 oz box UPC 0 15000 01015 7 GERBER PRODUCTS CO., FREMONT, MI 49413
    Category
    Food
    Distribution
    46 states
  • SevereNHTSA·25V143000·2025-03-05

    Airstream Recalls Classic Travel Trailers Due to Fire Risk

    Airstream is recalling certain Classic travel trailers because the sofa footrest switch wiring may overheat, increasing the risk of a fire.

    Product
    AIRSTREAM — AIRSTREAM CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0246-2025·2025-03-05

    Estradiol Gel Recalled Nationwide for Defective Packet Sealing

    Padagis US LLC recalls Estradiol Gel 0.1% nationwide due to defective packets that may not be fully sealed, potentially allowing ethanol loss.

    Product
    Estradiol Gel, 0.1%, 0.25 mg/g, 30 packets per carton, Rx Only, For Topical Use Only, Manufactured by Padagis, Yeruham, Israel, NDC: 45802-0134-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1238-2025·2025-03-05

    Pentax EPK-i8020c Video Processor Recalled for Thermal Burn Risk

    Pentax EPK-i8020c video processors can overheat during endoscopic procedures, creating a risk of thermal burns to patient tissues. The light guide tip becomes hot and may cause injury to mucous membranes.

    Product
    Pentax Medical Video Processor- Intended to be used with PENTAX Medical endoscopes, monitors and other peripheral devices for endoscopic diagnosis, treatment, and video observation. Model: EPK-i8020c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1207-2025·2025-03-05

    Automated Medication Cabinet Recalled Due to Fingerprint Scanner Overheating Risk

    CareFusion's BD Pyxis MedFlex automated medication cabinet is being recalled due to fingerprint scanner failure and overheating, posing a potential fire hazard in clinical settings.

    Product
    BD Pyxis MedFlex 2.0 REF 1139-00 Bio-ID Spare Parts REF 353200-01 The BD Pyxis" MedFlex is an Automated Dispensing Cabinet (ADC) intended to securely store and dispense medications and supplies to a qualified and authorized user in a clinical setting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1209-2025·2025-03-05

    Anatomic Lateral Fibula Plate recalled for locking screw malfunction

    Tyber Medical is recalling A.L.P.S. mvX Anatomic Lateral Fibula Plates due to reports of locking screws passing through the locking hole during surgery, causing surgical delays.

    Product
    A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate, 4-hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708041
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1226-2025·2025-03-05

    Medial Tibia Plate Recall Due to Locking Screw Malfunction During Surgery

    Tyber Medical recalls 109 units of the A.L.P.S. mvX Medial Tibia Plate nationwide due to reports of the locking screw passing through the locking hole during surgery, causing surgical delays.

    Product
    A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H RT -Medial Tibia Plate, 16-Hole, Right Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770715162
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1239-2025·2025-03-05

    MRI Systems Allow Unsafe Scan Resumption Exceeding SAR Safety Limits

    GE Healthcare MRI systems may incorrectly resume scans after power loss when tissue heating rates exceed safe limits, risking excessive heating if patients contact conductive materials or have implants.

    Product
    SIGNA Creator, SIGNA Explorer, NMRI systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1213-2025·2025-03-05

    Orthopedic plate recall: locking screw may pass through hole during surgery

    Tyber Medical is recalling 214 units of A.L.P.S. mvX orthopedic plates (nationwide) because the locking screw may pass through the locking hole during surgery. Surgical delays have been reported.

    Product
    A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate, 8-hole, Left Intended to bridge or otherwise stabilize bone fragments to facilitate healing. Model/Catalog Number: 770708081
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1212-2025·2025-03-05

    A.L.P.S. mvX Fibula Plate Recall: Locking Screw Malfunction During Surgery

    Tyber Medical is recalling 408 units of the A.L.P.S. mvX Anatomic Lateral Fibula Plate because the locking screw can pass through the locking hole during surgery, causing surgical delays. No injuries have been reported.

    Product
    A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate, 6-hole, Right Model/Catalog Number: 770708062
    Category
    Medical Device
    Distribution
    Distributed nationwide