The Recall Desk

State

Vermont product recalls

20,083 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.

6051–6075 of 20083

  • HighFDA (Food)·F-0527-2025·2025-02-12

    FGF LLC Bavarian Bismark pastry items recalled for potential listeria contamination

    FGF LLC is recalling Bavarian Bismark pastry item 8201936 due to potential listeria monocytogenes contamination. The recall covers all product within expiration produced on or before December 13, 2024, distributed nationwide in the US and Canada.

    Product
    item 8201936 NATURAL & ARTIFICIAL FLAVORED BAVARIAN BISMARK, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0480-2025·2025-02-12

    French Crullers Recalled Nationwide for Potential Listeria Contamination

    FGF, LLC is recalling French Crullers sold nationwide and in Canada due to potential Listeria monocytogenes contamination. All product with expiration dates from 12/13/24 and earlier is affected.

    Product
    item 8201812 FRENCH CRULLERS 72x 1.6 OZ, NET WT 6.48 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0521-2025·2025-02-12

    FDA Recalls Apple Crisp Cake Donuts for Potential Listeria Contamination

    FGF, LLC recalls Apple Crisp Cake Donuts for potential Listeria monocytogenes contamination. Approximately 2,017,614 cases are affected.

    Product
    item 8201920 APPLE CRISP CK DONUT PFD 78x3OZ, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V901000·2025-02-12

    2024 Hyundai Kona: Battery Cable Chafing May Cause Engine Fire

    Hyundai is recalling 2024 Kona vehicles because battery cables may chafe and short circuit, increasing the risk of engine compartment fire. Dealers will install protective sheathing at no cost.

    Product
    HYUNDAI — 2024 HYUNDAI KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0477-2025·2025-02-12

    FGF Plain Cake Donuts Recalled Due to Potential Listeria Contamination

    FGF, LLC is recalling 2,017,614 cases of plain cake donuts distributed nationwide in the US and Canada due to potential contamination with Listeria monocytogenes. No illnesses have been reported.

    Product
    item 8201809 PLAIN CAKE DONUT 108x2.25 OZ, NET WT 13.67 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1046-2025·2025-02-12

    X-Ray Imaging System May Continue Exposure Beyond Safety Limit

    GE Medical Systems' Optima XR646 HD X-Ray imaging systems may allow continued radiation exposure beyond the safety limit without operator confirmation. A warning message displays but does not prevent the excess exposure.

    Product
    Optima XR646 HD. X-Ray imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0488-2025·2025-02-12

    Yeast Ring Donuts Recalled Due to Listeria Contamination Risk

    FGF, LLC is recalling 2,017,614 cases of yeast ring donuts distributed nationwide and in Canada due to potential Listeria monocytogenes contamination. Consumers should not consume the product.

    Product
    item 8201836 GEN YST RING DONUT ZGT PFD 78x3OZ, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1111-2025·2025-02-12

    Temporary Titanium Abutments May Fracture in Dental Implants

    DDS Lab temporary titanium abutments may have been installed in some dental implant restoration cases instead of definitive abutments. The components may fracture, risking restoration loosening, oral tissue injury, and aspiration.

    Product
    Temporary Titanium Abutments
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0506-2025·2025-02-12

    FGF Fluff Donuts Recalled for Potential Listeria Contamination

    FGF, LLC is recalling 2,017,614 cases of item 8201870 Fluff Donuts due to potential Listeria monocytogenes contamination. The affected product was produced on or before December 13, 2024, and distributed nationwide in the US and Canada.

    Product
    item 8201870 GEN BAR FLUFF DONUT ZGT PFD 78x3OZ, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0529-2025·2025-02-12

    FGF Vanilla Mini Cake Donut Rings Recalled for Listeria Contamination Risk

    FGF, LLC is recalling 2,017,614 cases of vanilla mini cake donut rings due to potential Listeria monocytogenes contamination. The affected product was produced on or before December 13, 2024, and distributed nationwide in the US and Canada.

    Product
    item 8202891 PLAIN VANILLA MINI CAKE DONUT RING BULK 240X1.25OZ, NET WT 16.88 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0503-2025·2025-02-12

    FGF Pumpkin Cake Rings Recalled Due to Listeria Contamination Risk

    FGF's Just Baked Pumpkin Cake Rings are being recalled due to potential listeria monocytogenes contamination. Consumers should discard the product or return it to the point of purchase.

    Product
    item 8201866 JUST BAKED PUMPKIN CAKE RINGS 144x2.45 OZ, NET WT 22.05 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0215-2025·2025-02-12

    Prescription Carvedilol recalled for manufacturing impurity exceeding FDA specifications

    Glenmark Pharmaceuticals is recalling Carvedilol 25 mg tablets nationwide due to a manufacturing quality issue with impurity levels exceeding FDA recommended limits. Multiple lot numbers and expiration dates from February 2025 through February 2026 are affected.

    Product
    CARVEDILOL — CARVEDILOL (CARVEDILOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1101-2025·2025-02-12

    Dental implants recalled for manufacturing defect affecting sterile packaging

    Nobel Biocare recalled N1 TiUltra TCC dental implants due to a manufacturing defect that may puncture the sterile blister packaging. The defect is a sharp pin created during injection molding that could compromise product sterility.

    Product
    . Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Biocare N1 TiUltra TCC RP 4.0x11mm . Nobel Biocare N1 TiUltra TCC RP 4.0x13mm Nobel Biocare N1 TiUltra TCC implants are intended for use as an endosseous dental implant in the maxilla or mandible for anchoring or supporting
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1076-2025·2025-02-12

    Philips Allura CV20 patient tables risk finger entrapment during repositioning

    The Philips Allura CV20 System patient tables (AD7 and AD7X models) pose a finger entrapment hazard during manual repositioning. Fingers can become caught between the tabletop and guiding rails, potentially injuring operators and service personnel.

    Product
    Allura CV20 System Code: 722031
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1095-2025·2025-02-12

    Hologic Rapid fFN Specimen Collection Tubes May Contain Incorrect Extraction Buffer Volumes

    Hologic Rapid fFN Specimen Collection Tubes from three lots may contain incorrect amounts of extraction buffer, potentially causing invalid test results or diagnostic errors in preterm delivery assessment.

    Product
    The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of the Rapid fFN Specimen Collection kit (PN: 71738-001). The Collection Tube (PN: 71550-001) is manufactured by a third-party supplier, MML Diagnostics Packaging, and includes the transport tube, cap, and extr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1102-2025·2025-02-12

    ECG cable shipped with incomplete cleaning and disinfection instructions

    Physio-Control is recalling 245 LIFEPAK 35 ECG cables (Lot 0224) because the shipped instructions do not include proper cleaning and disinfection procedures, creating potential cross-contamination risks.

    Product
    LIFEPAK 35 ECG cable REF 11111-000041
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0526-2025·2025-02-12

    Apple Fritter Donuts Recalled for Potential Listeria Contamination

    FGF, LLC is recalling Apple Fritter Donuts (item 8201927) due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.

    Product
    item 8201927 APPLE FRITTER DONUT PFD 70 X 3.5OZ, NET WT 13.78 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0502-2025·2025-02-12

    Just Baked Apple Fritters Recalled Due to Listeria Contamination Risk

    FGF, LLC is recalling Just Baked Apple Fritters nationwide due to potential Listeria monocytogenes contamination. Consumers should discard affected products.

    Product
    item 8201865 JUST BAKED APPLE FRITTERS 72x3OZ, NET WT 13.50 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1115-2025·2025-02-12

    Beckman Coulter DxI 9000 immunoassay analyzer recalled for software-related motion errors

    Beckman Coulter is recalling 61 DxI 9000 immunoassay analyzers worldwide due to a software error causing tray gripper motion errors that result in intermittent hard stops and delays in patient test results.

    Product
    Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137; in-vitro diagnostic instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0512-2025·2025-02-12

    FGF LLC Recalls Unfilled Bismarck Donuts for Listeria Contamination Risk

    FGF LLC is recalling 2,017,614 cases of unfilled Bismarck donuts nationwide due to potential listeria monocytogenes contamination. Consumers should not consume the affected product.

    Product
    item 8201883 UNFLD BISMARK DONUT PFD 57x2.75OZ, NET WT 8.82 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0528-2025·2025-02-12

    Unfilled Bismarck Donuts Recalled Due to Listeria Contamination Risk

    FGF, LLC is recalling over 2 million cases of unfilled Bismarck donuts due to potential Listeria monocytogenes contamination. The recall affects products distributed nationwide in the US and Canada.

    Product
    item 8202731 UNFLD BISMARK DONUT PFD 78X3OZ, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1083-2025·2025-02-12

    Philips AlluraXper Operating Room Table Finger Entrapment Hazard

    The Philips AlluraXper FD20 operating room table can trap fingers between the guiding rails and tabletop during manual repositioning, potentially injuring operators and service personnel.

    Product
    AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0504-2025·2025-02-12

    Just Baked Pumpkin Cake Munchkins recalled for potential Listeria contamination

    FGF, LLC is recalling Just Baked Pumpkin Cake Munchkins nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume this product.

    Product
    item 8201867 JUST BAKED PUMPKIN CAKE MUNCHKINS 440x0.47 OZ, NET WT 12.93 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1084-2025·2025-02-12

    Philips Allura and Azurion Patient Tables Recall Due to Finger Entrapment Risk

    Philips is recalling AD7 and AD7X patient tables used in Allura and Azurion medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel are at risk of finger injury.

    Product
    AlluraXperFD20/10 System Code: (1) 722029
    Category
    Medical Device
    Distribution
    Distributed nationwide