The Recall Desk

State

Vermont product recalls

20,072 recalls have nationwide distribution and so reach Vermont. 0 additional recalls listed Vermont specifically in their distribution scope.

About recalls in Vermont

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Vermont consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

5426–5450 of 20072

  • HighNHTSA·25V573000·2025-04-09

    2025 Chrysler Pacifica side curtain air bags recalled for inadequate pressure retention

    Chrysler is recalling certain 2025 Pacifica and Voyager vehicles due to defective side curtain air bags. The air bags may have insufficient pressure retention from improperly sealed seams, increasing the risk of ejection during a crash.

    Product
    CHRYSLER — 2025 CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V654000·2025-04-09

    2024 RAM 2500 Rearview Camera Display Software Malfunction Recall

    Chrysler recalls 2024 RAM 2500 vehicles due to radio software that may prevent the rearview camera from displaying. Loss of rearview visibility increases crash risk.

    Product
    RAM — 2024 RAM 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1471-2025·2025-04-09

    Nasopore Standard Nasal Dressing Recalled Due to Sterility Seal Defects

    Stryker is recalling 182,344 units of Nasopore Standard nasal dressings nationwide due to potential bubbles in blister seals that may breach the sterility barrier and increase contamination risk.

    Product
    Nasopore Standard 8cm fragmentable nasal dressing, Catalog Numbers 5400-010-008 and 5400-010-008ITL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1482-2025·2025-04-09

    Stryker nasal wound dressing recalled for defective sterile packaging seal

    Stryker Corporation is recalling 182,344 units of Hemopore 2PK nasal/sinus wound dressing due to potential bubbles in blister seals that indicate sterility breach. Affected lot numbers are 2024020221, 2024051720, and 2024082321.

    Product
    Hemopore 2PK nasal/sinus temporary wound dressing, Catalog Number 5400-222-208S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1470-2025·2025-04-09

    Nasopore nasal dressing may have compromised sterile packaging

    Stryker is recalling Nasopore Standard 4cm nasal dressings because the blister seals may develop bubbles, potentially compromising the sterility barrier. Affected units should not be used.

    Product
    Nasopore Standard 4cm fragmentable nasal dressing, Catalog Numbers 5400-010-004 and 5400-010-004ITL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0685-2025·2025-04-09

    SeaBear Clam Chowder Recalled for Potential Botulinum Contamination

    SeaBear Smokedhouse Alehouse Clam Chowder pouches are recalled nationwide due to potential seal failure that could allow Clostridium botulinum contamination. Consumers should not consume the product.

    Product
    SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label, item 60104, Alehouse Chowder 12/CS.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1515-2025·2025-04-09

    Ethicon PROLENE BLU Surgical Sutures Recalled for Manufacturing Defect

    Ethicon is recalling specific lots of PROLENE BLU surgical sutures due to silicone curing issues during needle manufacturing.

    Product
    PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1516-2025·2025-04-09

    Surgical Suture Recall Due to Silicone Curing Defect

    Ethicon Endo Surgery recalls ETHIBOND EXCEL surgical sutures worldwide due to curing issues with the silicone coating on the needles identified during manufacturing.

    Product
    ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V580000·2025-04-09

    IC Bus School Buses Recalled for Structural Reinforcement Defect

    International Motors is recalling certain 2016-2026 IC Bus CESB and 2016-2021 RESB school buses due to missing or incomplete underfloor reinforcement that may compromise crash safety. Owners should contact a dealer for free inspection and installation.

    Product
    IC BUS — 2020 IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1474-2025·2025-04-09

    Nasopore nasal dressing recall: compromised sterile barrier seals

    Stryker recalls Nasopore 4cm fragmentable nasal dressings due to potential blister seal damage that compromises the sterile barrier. Nationwide distribution affected.

    Product
    Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1506-2025·2025-04-09

    Medtronic A820 myPTM Infusion Pump Software Shows Delayed Patient Response

    Medtronic is recalling the A820 myPTM Software Application used with SynchroMed infusion pumps because the app is taking longer than expected to respond to patient interactions. Approximately 4365 units are affected worldwide.

    Product
    A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V576000·2025-04-09

    Jeep Grand Cherokee Plug-In Hybrid Software Error Causes Loss of Drive Power

    Chrysler recalls certain 2022-2026 Jeep Grand Cherokee plug-in hybrids for a software error in the hybrid control processor that may cause loss of drive power and increase crash risk.

    Product
    JEEP — 2023 JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0308-2025·2025-04-09

    Prescription Duloxetine Capsules Recalled for Nitrosamine Impurity

    Breckenridge Pharmaceutical is recalling Duloxetine 30 mg capsules distributed nationwide due to a nitrosamine impurity above acceptable limits. Consumers should consult their doctor about their medication.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0307-2025·2025-04-09

    Voriconazole Tablets Recalled Due to Manufacturing Practice Deviations

    Amerisource Health Services is recalling Voriconazole 50 mg tablets distributed nationwide due to current Good Manufacturing Practice deviations related to repackaging.

    Product
    VORICONAZOLE — VORICONAZOLE (VORICONAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0304-2025·2025-04-09

    Tolterodine Tartrate Extended-Release Capsules Recalled for Failed Dissolution

    Tolterodine Tartrate Extended-Release Capsules, 2 mg (Lot T05393) are being recalled because they failed dissolution specifications. The capsules may not dissolve as intended.

    Product
    TOLTERODINE TARTRATE — TOLTERODINE TARTRATE (TOLTERODINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0309-2025·2025-04-09

    Prescription Antipsychotic Drug Recalled for Manufacturing Impurity

    Glenmark Pharmaceuticals is recalling Chlorpromazine Hydrochloride Tablets due to a manufacturing quality deviation involving an impurity above recommended limits.

    Product
    CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1513-2025·2025-04-09

    Surgical Suture Needles Recalled Due to Manufacturing Defect

    Ethicon Endo Surgery recalls PDS PLUS VIO surgical sutures with needles due to silicone curing defects during manufacturing. 792 units were distributed worldwide.

    Product
    PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V499000·2025-04-08

    2024-2025 Winnebago Ekko RV Tire Valve Extension Defect Recall

    Winnebago is recalling certain 2024-2025 Ekko recreational vehicles due to damaged tire valve extensions that can cause air loss in the inner tire and overload the outer tire, creating a crash risk. Dealers will replace the extensions free of charge.

    Product
    WINNEBAGO — 2024 WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V533000·2025-04-07

    2024 Porsche Cayenne Front Suspension Control Arm May Crack and Fail

    Porsche is recalling 2,475 2024 Cayenne vehicles due to potentially cracked driver's side front upper control arms that may break and cause loss of steering control.

    Product
    PORSCHE — 2024 PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V449000·2025-04-06

    2022-2023 BMW I4 Recalled for High Voltage Battery Charging Unit Failure

    BMW recalls certain 2022-2023 I4, iX, and i760 models due to a defective high voltage battery charging unit that may not have been properly assembled, potentially causing engine stall while driving.

    Product
    BMW — 2022 BMW I4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V324000·2025-04-06

    2025 Nissan Frontier rear display may blank in reverse

    The 2025 Nissan Frontier's center information display may show a blank screen in reverse, violating federal rear-visibility standards. This could reduce driver visibility and increase crash risk.

    Product
    NISSAN — 2025 NISSAN FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V452000·2025-04-06

    Certain 2021–2025 Lion LionC School Buses Electrical Hardware Recall

    Lion Electric is recalling 2021–2025 LionC school buses due to loose electrical hardware that could cause short circuits and loss of steering or braking power. Contact Lion customer service at 1-855-546-6706 for free replacement.

    Product
    LION — 2021 LION LIONC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V336000·2025-04-06

    Mazda MX-5 recalled for Dynamic Stability Control indicator light failure

    Mazda is recalling 2024-2025 MX-5 vehicles where the Dynamic Stability Control indicator light may fail to illuminate due to a software error. This could prevent drivers from being warned of a traction control system failure, increasing crash risk.

    Product
    MAZDA — 2025 MAZDA MX-5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V346000·2025-04-05

    2024 Jeep Grand Cherokee: Missing Bumper Foam May Prevent Airbag Deployment

    Certain 2024 Jeep Grand Cherokees may be missing foam in the front bumper, which could prevent the front airbags from deploying during a crash. Dealers will install the foam at no cost.

    Product
    JEEP — 2024 JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide