The Recall Desk

State

Vermont product recalls

73,213 recalls have nationwide distribution and so reach Vermont. 2,009 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total
2,009
Critical
209
Severe
419
Most recent
2026-09-23

Of the 2,009 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 419 (21%) are Severe.

These figures cover only the 2,009 recalls whose distribution notice names Vermont specifically. The 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13826–13850 of 75222

  • HighFDA (Drugs)·D-0122-2024·2023-12-06

    Paroxetine Hydrochloride Tablets Recalled for Out-of-Specification Impurity

    Apotex Corp. is recalling Paroxetine Hydrochloride 40 mg tablets nationwide due to failed quality specifications. Testing found out-of-specification impurity levels in affected lot numbers.

    Product
    PAROXETINE — PAROXETINE (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V818000·2023-12-06

    KME Recalls 2020 Fire Trucks Due to Electrical Fire Risk

    Kovatch Mobile Equipment is recalling 2020 Severe Service, Predator, and Spartan MetroStar trucks because a firmware defect may cause electrical fires.

    Product
    KME — KME, SPARTAN FIRE SEVERE SERVICE, PREDATOR, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0400-2024·2023-12-06

    BD Insyte Autoguard IV Catheter Needles May Fail to Retract Properly

    BD Insyte Autoguard BC IV catheters may have needles that fail to retract properly, potentially causing contaminated needlestick injuries, blood leakage, and repeated insertion attempts.

    Product
    BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V820000·2023-12-06

    Ducati Recalls XDiavel Motorcycles Due to Passenger Backrest Defect

    Ducati is recalling 2016-2023 XDiavel S and STD motorcycles because the passenger backrest may break, increasing the risk of the passenger falling off.

    Product
    DUCATI — DUCATI XDIAVEL STD, XDIAVEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0123-2024·2023-12-06

    Prescription Drug Indomethacin Recalled Due to Label Mix-Up

    Glenmark Pharmaceuticals is recalling 37,200 bottles of Indomethacin 25mg capsules distributed nationwide because the bottles may be labeled as Naproxen instead. This labeling error could cause medication confusion.

    Product
    INDOMETHACIN — INDOMETHACIN (INDOMETHACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0423-2024·2023-12-06

    RAPIDPOINT 500 Blood Gas System: Drug Interference May Cause False Sodium Readings

    Siemens RAPIDPOINT 500 Blood Gas System may produce falsely elevated sodium results due to drug interference from Perhexiline Maleate or Atomoxetine Hydrochloride. This could lead to missed hyponatremia or inappropriate treatment of hypernatremia.

    Product
    RAPIDPOINT 500 Blood Gas System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0422-2024·2023-12-06

    RAPIDPOINT 500e Blood Gas System Recalled Due to Drug Interference

    Siemens RAPIDPOINT 500e blood gas systems may show falsely elevated sodium readings in patients taking Perhexiline Maleate or Atomoxetine, risking misdiagnosis and inappropriate treatment of electrolyte imbalances.

    Product
    RAPIDPOINT 500e Blood Gas System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0130-2024·2023-12-06

    Paroxetine 40 mg tablets recalled for out-of-specification impurities

    Golden State Medical Supply Inc. is recalling Paroxetine 40 mg tablets due to failed impurity specifications. A total of 5,626 bottles were distributed nationwide.

    Product
    PAROXETINE — PAROXETINE (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0125-2024·2023-12-06

    Compounded Ophthalmic Medication Bottles Mislabeled as Single-Use Syringes

    Fagron Compounding Services is recalling 756 bottles of compounded ophthalmic medication because labels incorrectly identify the container as a 0.5mL single-use syringe instead of a 5mL dropper bottle. No adverse events have been reported.

    Product
    Tropicamide 1% (10mg/mL), Cyclopentolate 1% (10mg/mL), Phenylephrine 2.5% (25mg/mL), Ketorolac 0.5% (5mg/mL), 5 mL bottles, For Topical Ophthalmic Use Only, Not for IV Use, This is a Compounded Drug, Hospital & Office Use Only, Fagron Sterile Services, 8710 E 34th St N Wichita…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0129-2024·2023-12-06

    Paroxetine 20 mg Tablets Recalled for Out-of-Specification Impurity

    Golden State Medical Supply is recalling certain lots of Paroxetine 20 mg tablets nationwide due to an out-of-specification chemical impurity in the product.

    Product
    PAROXETINE — PAROXETINE (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0127-2024·2023-12-06

    Testosterone Gel Recalled for Out-of-Specification Viscosity

    Teva Pharmaceuticals recalls specific lots of Testosterone Gel 1.62% for failing viscosity specifications. Patients should contact their healthcare provider to discuss the recall and obtain unaffected medication.

    Product
    TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0126-2024·2023-12-06

    VistaPharm Recalls Aminocaproic Acid Oral Solution Due to High Ethylene Glycol

    VistaPharm LLC is recalling Aminocaproic Acid Oral Solution (0.25 grams/mL) distributed nationwide due to high ethylene glycol content from failed manufacturing specifications. Four lot numbers are affected.

    Product
    Aminocaproic Acid Oral Solution, 0.25 grams/mL, Rx only, packaged in 8 Fl. Oz. (236.5 mL) HDPE bottles, Manufactured for: VistaPharm, Inc., Largo, FL 33771, UAS, NDC 66689-330-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0120-2024·2023-12-06

    Paroxetine Tablets Recalled Due to Manufacturing Specification Failure

    Apotex Corp. is recalling Paroxetine Hydrochloride 20 mg tablets nationwide due to out-of-specification impurity levels in affected lots. No illnesses have been reported.

    Product
    PAROXETINE — PAROXETINE (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V815000·2023-12-05

    Terberg Benschop Recalls Terminal Tractors for Steering Linkage Defect

    Terberg Benschop is recalling 2021-2022 YT193 terminal tractors because paint wear on the steering linkage may cause bolts to loosen or break, risking loss of steering control.

    Product
    TERBERG BENSCHOP B.V. — TERBERG BENSCHOP B.V. TERMINAL TRACTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V817000·2023-12-05

    Cushman Recalls 2024 Hauler Pro LSVs Due to Fire Risk

    Textron Specialized Vehicles is recalling 2024 Cushman Hauler Pro LSVs because water may enter the battery module, damaging circuits and increasing fire risk.

    Product
    CUSHMAN — CUSHMAN HAULER PRO LSV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24726·2023-12-05

    Foiresoft Zebra Roller Blinds Recalled for Strangulation Hazard

    Foiresoft Zebra Roller Blinds sold on Amazon.com have looped operating cords that pose a strangulation hazard to children. Consumers should stop using them immediately and contact Softfunch for a refund.

    Product
    Foiresoft Zebra Roller Blinds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V816000·2023-12-05

    Volvo 2024 VN and VHD: Incorrect Axle Weight Label Increases Overload Risk

    Certain 2024 Volvo VN and VHD trucks have an incorrect Gross Axle Weight Rating label, which can allow vehicles to be overloaded and increases crash risk. Dealers will replace the label free of charge.

    Product
    VOLVO — VOLVO VN, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V811000·2023-12-04

    Eldorado Axess and EZR Buses Recalled for Driveshaft Separation Risk

    Eldorado is recalling 2019-2023 Axess and EZR buses because a transmission yoke may separate, causing a sudden loss of drive power and increasing crash risk.

    Product
    ELDORADO — ELDORADO AXESS, EZR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V812000·2023-12-04

    Gillig Recalls 2021-2023 Low Floor Vehicles Due to Fire Risk

    Gillig is recalling 3,626 Low Floor vehicles from 2021-2023 because an incorrect fuse in the rearview mirror system may overheat and cause a fire.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V813000·2023-12-04

    Porsche Recalls 718 Models Due to Spoiler Visibility Issue

    Porsche is recalling certain 2023-2024 718 models because the rear spoiler may raise too high, reducing brake light visibility and increasing crash risk.

    Product
    PORSCHE — PORSCHE 718 BOXSTER S, 718 CAYMAN GTS, 718 BOXSTER GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V814000·2023-12-04

    2023 INFINITI QX60 Headlight System Malfunction Increases Crash Risk

    Nissan is recalling certain 2023-2024 INFINITI QX60 vehicles because the Adaptive Front-Light System may incorrectly adjust headlights downward at high speeds, reducing visibility and increasing crash risk.

    Product
    INFINITI — INFINITI QX60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V807000·2023-12-01

    Mercedes-Benz Recalls 2024 GLE 450e Due to Stopping Distance Issue

    Mercedes-Benz is recalling 2,797 2024 GLE 450e vehicles because a software error may increase the distance required to stop, raising crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450E 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V808000·2023-12-01

    Spartan Fire Recalls 2020-2023 Fire Apparatus Due to Electrical Fire Risk

    Spartan Fire is recalling 69 fire apparatus units from 2020-2023 because a firmware defect may cause electrical circuits to overheat and start a fire.

    Product
    KME — KME, SPARTAN FIRE, SMEAL AERIAL FIRE APPARATUS, S-180 PUMPER, AERIAL, PUMPER FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide