The Recall Desk

State

US Virgin Islands product recalls

73,218 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
30
Most recent
2026-09-23

Of the 177 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16976–17000 of 73395

  • HighFDA (Devices)·Z-1153-2023·2023-03-01

    ADVIA Centaur Folate 500 test kits recalled for inaccurate measurement results

    Siemens Healthcare Diagnostics is recalling 7,884 ADVIA Centaur Folate 500 diagnostic test kits because using whole blood calibration with serum samples produces negative bias and inaccurate results.

    Product
    ADVIA Centaur Folate 500 test kit- For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 10325366
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1151-2023·2023-03-01

    Atellica IM Folate test kit recalled for measurement bias issues

    Siemens Healthcare is recalling 1,865 Atellica IM Folate 700 diagnostic kits nationwide and internationally. The kits may produce inaccurate folate test results when whole blood calibration is used instead of serum calibration.

    Product
    Atellica IM Folate 700 test kit (REF)-For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 11206252
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1160-2023·2023-03-01

    Respiratory care breathing circuits recalled for incorrect expiration date labeling

    S & MOHR AMERICA recalled approximately 1,320 abm Respiratory Care Standard Breathing Circuits due to incorrect expiration dates printed on product labels. The manufacturing date was printed where the expiration date should appear.

    Product
    abm Respiratory Care Standart Breating Circuit with Face Mask - Toddler REF BC21087 abm Respiratory Care Standart Breathing Circuit with Face Mask - Child/Adult Small REF BC21088 abm Respiratory Care Standart Breathing Circuit with Face Mask - Adult Large REF BC21273…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0343-2023·2023-03-01

    TIROSINT levothyroxine sodium oral solution recalled for subpotency nationwide

    IBSA Pharma Inc. is recalling TIROSINT (levothyroxine sodium) oral solution due to subpotency—some doses contain insufficient active ingredient. Patients should contact their pharmacist or doctor to verify their medication.

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0333-2023·2023-03-01

    TIROSINT Levothyroxine Oral Solution Recalled for Subpotent Drug Content

    IBSA PHARMA INC is recalling TIROSINT oral solution (Lot #220855) nationwide due to insufficient potency of levothyroxine sodium. The defective lot was voluntarily recalled after manufacturer discovery.

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0329-2023·2023-03-01

    OTC First Aid Spray Recalled for Subpotent Active Ingredient

    Dermoplast FIRST AID spray is being recalled because testing found low levels of one of its two active ingredients. The product was distributed nationwide through internet, distributors, and retailers.

    Product
    DERMOPLAST FIRST AID — DERMOPLAST FIRST AID (BENZETHONIUM CHLORIDE AND BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0344-2023·2023-03-01

    TIROSINT Levothyroxine Oral Solution Recalled for Subpotency

    IBSA Pharma has recalled one lot of TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotency. The product contained less active ingredient than labeled.

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V132000·2023-02-28

    Hyundai Recalls 2012-2014 Veloster Vehicles Due to Electrical Fire Risk

    Hyundai is recalling 2012-2014 Veloster vehicles because high conductive liquid may leak into the Reverse Park Aid Sensor, causing an electrical short circuit and increasing fire risk.

    Product
    HYUNDAI — HYUNDAI VELOSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V131000·2023-02-28

    2023 Nissan Ariya recalled for potentially loose steering wheel bolts

    Nissan North America is recalling 2023 Ariya vehicles with potentially loose or missing steering wheel bolts. A detached steering wheel could cause loss of steering control and increase crash risk.

    Product
    NISSAN — NISSAN redundant ARIYA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V130000·2023-02-27

    Tesla Recalls 2022-2023 Model Y Vehicles for Loose Seat Bolts

    Tesla is recalling 2022-2023 Model Y vehicles because second-row seat back frame bolts may not be securely tightened, potentially reducing seat belt performance.

    Product
    TESLA — TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V129000·2023-02-27

    Royal Enfield Himalayan motorcycles recalled for brake caliper corrosion

    Royal Enfield is recalling 2017-2021 Himalayan motorcycles because road salt may corrode brake calipers, potentially causing brake failure and increasing crash risk.

    Product
    ROYAL ENFIELD — ROYAL ENFIELD HIMALAYAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V126000·2023-02-24

    Prevost Recalls Motor Coaches Due to Fire Suppression Sensor Defect

    Prevost is recalling 2018-2023 H3-45 and 2019 H3-41 vehicles because a fire sensor may corrode, causing sudden engine shutdown and crash risk.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45, H3-41
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V128000·2023-02-24

    2023 Ford Expedition front axle may fracture, increasing crash risk

    Ford is recalling certain 2023 Expeditions, along with F-150 and Lincoln Navigator vehicles, due to a front axle pinion defect that may not have been properly heat-treated. The defect can cause fracture, loss of 4-wheel drive, and wheel lockup, increasing crash risk.

    Product
    FORD — FORD, LINCOLN F-150, EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V121000·2023-02-24

    Thor Motor Coach recreational vehicles recalled for detaching overhead cabinets

    Thor Motor Coach is recalling 2018-2021 Windsport and Hurricane recreational vehicles because the driver and front passenger overhead cabinets may detach while in motion, risking injury to occupants.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V123000·2023-02-24

    2023 BMW S 1000 RR Motorcycles Recalled for Hand Brake Defect

    BMW of North America is recalling certain 2023 S 1000 RR motorcycles due to a hand brake lever defect that may reduce brake performance. Approximately 394 units are affected.

    Product
    BMW — BMW S 1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23136·2023-02-23

    LumaRail Bed Assist Rails recalled for entrapment and asphyxia hazard

    Platinum Health is recalling about 53,000 LumaRail bed assist rails because users can become entrapped between the rail and mattress, risking death by asphyxiation. One death has been reported.

    Product
    LumaRail Bed Assist Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V117000·2023-02-23

    Braun Recalls Demers Ambulances Due to Rear Step Welding Defect

    Braun Ambulances is recalling specific 2020 and 2022 Demers ambulances because the rear step may fail under weight due to incorrect welding, posing an injury risk.

    Product
    DEMERS — DEMERS MX170E, MXP153E, MXP170E, MXP170Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V120000·2023-02-23

    2022–2024 International and IC Bus Trucks/Buses: Engine Control Software Defect

    Navistar is recalling 2022-2024 International HV and MV trucks and 2022-2023 IC Bus TC buses. An engine control module software defect can cause the engine to override the parking brake when the transmission remains in drive or reverse and the power take-off switch is engaged, resulting in unintended vehicle movement.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS MV, TC, HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23135·2023-02-23

    Aderes Bookcases Recalled Due to Tip-Over and Entrapment Hazards

    TJX is recalling about 73 Aderes bookcases that can tip over if not anchored to the wall, posing tip-over and entrapment hazards that can result in death or injuries to children. Two reports of unstable bookcases have been received with no injuries reported.

    Product
    Aderes bookcases
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V118000·2023-02-23

    2022-2023 BMW M3 Door Locking Software Defect Recall

    BMW is recalling certain 2022-2023 models due to a door locking software defect. Faulty ECU programming may prevent doors from locking while driving, increasing crash injury risk.

    Product
    BMW — BMW I4, M440I, M340I, 430I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23133·2023-02-23

    1st Stage Scuba Regulators Recalled for Drowning and Injury Risk

    XDEEP 1st stage scuba regulators (model NX700) are recalled because a defective screw on the turret connection can break, creating a risk of severe injury and drowning for divers.

    Product
    1st stage scuba regulators
    Category
    Consumer Product
    Distribution
    Distributed nationwide