The Recall Desk

State

US Virgin Islands product recalls

72,969 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
2026-09-09

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.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6451–6475 of 73146

  • HighNHTSA·25V338000·2025-05-23

    Lincoln seat belt warning chime may sound for less than four seconds

    Ford is recalling certain 2020-2023 Lincoln Aviator and Corsair vehicles with Revel Audio, previously repaired under 22V-953, because the unbelted warning chime may sound for under four seconds.

    Product
    LINCOLN — LINCOLN AVIATOR, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V347000·2025-05-23

    Ford Recalls 2016-2017 Explorers for Detaching B-Pillar Door Trim

    Ford is recalling 2016-2017 Explorer vehicles because the driver and front passenger B-Pillar door trim may detach while driving, creating a road hazard.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V346000·2025-05-23

    Ford Recalls 2020 Expedition and Navigator for Software Error

    Ford is recalling 2020 Expedition and Navigator vehicles where previous repairs left pre-collision assist features inoperative due to a software error.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V348000·2025-05-23

    Ford Recalls 2021 F-150 Trucks for Inoperative Reverse Lights

    Ford is recalling 2021 F-150 trucks with Onboard Scales because a previous software update may have disabled the reverse lights, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V343000·2025-05-23

    Ford engine block heaters can overheat while plugged in and parked

    Ford is recalling certain 2023-2025 Escape, Maverick, Bronco Sport, Lincoln Nautilus and Corsair vehicles with engine block heaters because the heater may overheat when the vehicle is parked and plugged in.

    Product
    FORD — FORD, LINCOLN BRONCO SPORT, ESCAPE, MAVERICK, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V337000·2025-05-23

    Lincoln Nautilus displays can reboot leaving the driver a blank screen

    Ford is recalling certain 2024 Lincoln Nautilus vehicles because multimedia module software may cause the panoramic and centre displays to reboot, leaving a blank screen.

    Product
    LINCOLN — LINCOLN NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V197000·2025-05-23

    Ford Recalls 2018-2020 Expedition and Navigator for Seat Belt Defect

    Ford is recalling 2018-2020 Expedition and Lincoln Navigator vehicles because seat belt pretensioners may lock, preventing belts from retracting or extending.

    Product
    LINCOLN — LINCOLN, FORD NAVIGATOR, EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25290·2025-05-22

    Nezmdi Infant Swings Recalled for Suffocation Hazard and Safety Violations

    Nezmdi infant swings pose a suffocation risk because they exceed safe incline angles and were marketed for infant sleep. About 1,420 units sold on Amazon from September 2024 through February 2025 lack required safety warnings.

    Product
    Nezmdi Baby Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25292·2025-05-22

    Rolanstar 6-Drawer Dressers recalled for tip-over and entrapment hazards

    Rolanstar 6-Drawer Dressers sold on Amazon are unstable and pose serious tip-over and entrapment hazards to children if not anchored to the wall. About 1,293 units were sold between September 2023 and March 2025.

    Product
    Rolanstar 6-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25293·2025-05-22

    Sivan Six-Drawer Double Dressers Recalled for Tip-Over and Entrapment Hazards

    Sivan six-drawer double dressers can tip over without wall anchoring, posing serious injury or death risk to children. About 170 units sold on Wayfair from May 2024 to March 2025 are affected.

    Product
    Sivan Six-Drawer Double Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V335000·2025-05-22

    Shyft Recalls 2022-2024 Utilimaster Velocity Vehicles Missing Tire Placards

    Shyft Group is recalling 2022-2024 Utilimaster Velocity vehicles because they may be missing the tire and information placard, which is required by federal safety standards.

    Product
    UTILIMASTER — UTILIMASTER VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-05222025-01·2025-05-22

    USDA Issues Alert for Chicken Soup with Undeclared Wheat Allergen

    USDA FSIS issued a public health alert for Signature SELECT chicken soup cups containing undeclared wheat. Consumers with wheat allergies should not consume the products.

    Product
    FSIS Issues Public Health Alert for Chicken Soup Product Due To Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·25291·2025-05-22

    Holiday Lane Infant Footed Pajamas Recalled for Ankle Elastic Injury Hazard

    Macy's is recalling Holiday Lane Infant Footed Pajamas because the ankle elastic can be too tight, restricting blood circulation and causing injury. The company has received four reports of chafing, imprinting, or circulation restriction.

    Product
    Holiday Lane Infant Footed Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25E037000·2025-05-22

    Zoox Recalls Driverless Vehicles for Software Defect in Person Detection

    Zoox is recalling Automated Driving Systems with older software that may fail to detect people next to the vehicle, increasing injury risk.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25294·2025-05-22

    Primark DTR Plush Bag Stitch and Angel Recalled for Choking Hazard

    Primark is recalling DTR Plush Bag Stitch and DTR Plush Bag Angel products because the zipper pull can detach, posing a choking and ingestion risk to children.

    Product
    DTR Plush Bag Stitch and DTR Plush Bag Angel
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V336000·2025-05-22

    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 — MAZDA MX-5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0420-2025·2025-05-21

    Testosterone Cypionate Injection 200 mg/mL Recalled for Sterility Assurance

    Empower Pharmacy is recalling Testosterone Cypionate Injection 200 mg/mL (Lot 202364, 8,230 vials) distributed nationwide because the manufacturer cannot assure the product's sterility. Consumers should stop using the product and consult their healthcare provider.

    Product
    Testosterone Cypionate Injection, 200 mg/mL, CIII, Rx Only, 5 mL Sterile Multiple-Dose Vial, Compounded by: Empower Pharmacy, 7601 N Sam Houston Pkwy W Ste 100, Houston, TX, 77064, Phone: (877) 562-8577, Compounding Date: 08/20/2024, Beyond Use by Date: 05/28/2025, Lot 202364.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1727-2025·2025-05-21

    iGo2 DC Car Adapter Recall: Overheating and Housing Deformation Risk

    Medical Depot Inc. is recalling 89,532 units of the iGo2 DC Car Adapter used with iGo2 Portable Oxygen Concentrator Systems. The DC power supply housing may become excessively hot to the touch and deform, posing a burn and fire hazard.

    Product
    iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1698-2025·2025-05-21

    AirLife Infant Heated Wire Circuit Adapter Disconnection Risk Recall

    Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (model AH265) because adapters may disconnect during setup or use, potentially interrupting ventilation to newborns. Disconnection can cause hypoxia, hypercapnia, and organ failure.

    Product
    Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH265 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit Kit Dual-limb, Dual-heat, high-flow circuit (>4 L/min) Contains AH165 Circuit, AH290 Chamber Compone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1730-2025·2025-05-21

    MedicaLyte Liquid Bicarbonate Concentrate Recalled for Foreign Matter

    Nipro Renal Solutions USA is recalling MedicaLyte Liquid Bicarbonate Concentrate (models BC+201 and BC+100) due to the potential presence of visible foreign matter in the product.

    Product
    MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in corrugated shipper cases (4 bottles per shipper case).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1697-2025·2025-05-21

    AirLife Infant Heated Wire Circuit Adapter Disconnection Risk

    Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (Model AH165) because adapters may disconnect during setup or use, interrupting ventilation to infants and potentially causing severe complications.

    Product
    Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH165 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit dual-limb, dual-heat, high-flow circuit (>4 L/min) Component: No. a conduit for respiratory gas bet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1750-2025·2025-05-21

    TufTex Over-the-Wire Embolectomy Catheter incomplete sterile barrier

    LeMaitre Vascular is recalling TufTex Over-the-Wire Embolectomy Catheters due to incomplete seals on some packages that compromise the sterile barrier. Affected units were distributed nationwide and internationally.

    Product
    TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34, 1651-38, 1651-44, 1651-48, 1651-58, 1651-64, 1651-68, 1651-78, 1651-84, 1651-88, E1651-34, E1651-38, E1651-44, E1651-48, E1651-64, E1651-68, E1651-78, E1651-84, E1651-88, 1651-44J, 1651-48J, 1651-84J, 1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1763-2025·2025-05-21

    LifeShield Infusion Safety Software Recalled for Drug Library Defects

    ICU Medical is recalling LifeShield Drug Library Management software v2.1 and v2.2 due to defects that could allow over-delivery of medication to patients or unauthorized modification of drug parameters.

    Product
    LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2
    Category
    Medical Device
    Distribution
    Distributed nationwide