The Recall Desk

State

US Virgin Islands product recalls

73,722 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
178
Critical
12
Severe
39
Most recent
2026-10-21

Of the 178 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 39 (22%) are Severe.

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31576–31600 of 73900

  • SevereNHTSA·19V803000·2019-11-07

    Freightliner Cascadia Recall for Brake Chamber Clearance Defect

    Daimler Trucks North America is recalling 2020 Freightliner Cascadia vehicles because brake chambers may contact the frame rail, potentially causing detachment and reduced braking.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V798000·2019-11-07

    NHTSA Recalls 2019 Mercedes-Benz and Freightliner Sprinter Diesel Fuel Systems

    NHTSA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because a fuel system defect may cause diesel leaks or fuel overflow.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V802000·2019-11-07

    Hyundai Recalls 2020 Palisade Vehicles for Side Air Bag Defect

    Hyundai is recalling 2020 Palisade vehicles because mounting bolts may damage side curtain air bags, potentially preventing proper inflation in a crash.

    Product
    HYUNDAI — HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V801000·2019-11-07

    GM Recalls 2014-2016 Chevrolet SS for Steering Connector Corrosion

    General Motors is recalling 2014-2016 Chevrolet SS vehicles because corrosion in the steering connector may cause a loss of electric power steering assist, increasing the risk of a crash.

    Product
    CHEVROLET — CHEVROLET CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V799000·2019-11-07

    Thor Motor Coach Recalls Tuscany and Venetian Motorhomes for Visibility Defect

    Thor Motor Coach is recalling specific Tuscany and Venetian motorhomes because rear reflectors may be positioned too high, reducing vehicle visibility and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY, TUSCANY XTE, VENETIAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0203-2020·2019-11-06

    Ethicon Echelon Flex Powered Plus Stapler Recalled for Anvil Defect

    Ethicon Endo-Surgery Inc is recalling 2,112 Echelon Flex Powered Plus ENDOPATH 60mm Staplers worldwide due to out-of-specification anvil components that may compromise staple line integrity.

    Product
    ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 340mm shaft, Product Code PSEE60A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0160-2020·2019-11-06

    Innoveix Recalls Lyophilized Human Chorionic Gonadotropin Due to Sterility Concerns

    Innoveix Pharmaceuticals is recalling 290 vials of Lyophilized Human Chorionic Gonadotropin 5,500 USP Units due to a lack of sterility assurance.

    Product
    Lyophilized Human Chorionic Gonadotropin 5,500 USP Units For injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0201-2020·2019-11-06

    Ethicon Recalls ECHELON FLEX Staplers Due to Anvil Defect

    Ethicon Endo-Surgery Inc is recalling 255 units of the ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler because an out-of-specification anvil may cause malformed staples and compromised staple lines.

    Product
    ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 280mm shaft, Product Code PCEE60A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0221-2020·2019-11-06

    Thoratec CentriMag Motor Recalled Due to Electromagnetic Interference Issues

    Thoratec is recalling CentriMag Acute Circulatory Support System motors due to reports of motor and pump issues caused by electromagnetic interference.

    Product
    CentriMag Acute Circulatory Support System Motor, U.S. Model 102956 and OUS Model 201-10002, a component of the CentriMag Extracorporeal Blood Pumping System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0200-2020·2019-11-06

    Ethicon Echelon Flex Endopath Stapler Recall for Out-of-Spec Anvil

    Ethicon is recalling Echelon Flex Endopath 60mm Staplers due to out-of-specification anvil components that may compromise staple line integrity.

    Product
    ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft, Product Code EC60A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0159-2020·2019-11-06

    Innoveix Recalls Lyophilized Sermorelin Injection Due to Sterility Concerns

    Innoveix Pharmaceuticals is recalling 1,747 vials of compounded Sermorelin injection because the product lacks sterility assurance.

    Product
    Lyophilized Sermorelin w/ GHRP2 3 mg For injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0158-2020·2019-11-06

    Innoveix Recalls Lyophilized Human Chorionic Gonadotropin Due to Sterility Concerns

    Innoveix Pharmaceuticals is recalling 413 vials of Lyophilized Human Chorionic Gonadotropin 5,000 USP Units due to a lack of sterility assurance.

    Product
    Lyophilized Human Chorionic Gonadotropin 5,000 USP Units For injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0157-2020·2019-11-06

    Innoveix Recalls Lyophilized Chorionic Gonadotropin Due to Sterility Concerns

    Innoveix Pharmaceuticals is recalling 3,905 vials of Lyophilized Chorionic Gonadotropin 11,000 USP Units for Injection due to a lack of sterility assurance.

    Product
    Lyophilized Chorionic Gonadotropin 11,000 USP Units for Injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0202-2020·2019-11-06

    Ethicon Echelon Flex Powered Plus Endopath 60mm Stapler Recall

    Ethicon is recalling 5,040 Echelon Flex Powered Plus Endopath 60mm Staplers due to out-of-specification anvil components that may compromise staple line integrity.

    Product
    ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 440mm shaft, Product Code PLEE60A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V800000·2019-11-06

    Mercedes-Benz Sprinter Recall for Front Seat Weld Defect

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because a front seat weld may break in a crash, increasing injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0258-2020·2019-11-06

    Draeger Infinity Acute Care System Recalled for Cybersecurity Vulnerabilities

    Draeger Medical Systems is recalling 5,634 Infinity Acute Care System monitors due to cybersecurity vulnerabilities that may cause device reboots and loss of alarm functionality.

    Product
    The Infinity Acute Care System (IACS) Monitoring Solution with the Standalone Infinity M540 patient monitor. Model nos. MS25510, MS25520, MS26372.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0249-2020·2019-11-06

    Intuitive Surgical Recalls EndoWrist Suction Irrigator Due to Silicone Particle Risk

    Intuitive Surgical is recalling EndoWrist Suction Irrigator instruments because silicone particles may form and be introduced into patients during irrigation.

    Product
    EndoWrist Suction Irrigator, Single Use Instrument. Part Number: 480299-04. An accessory to the EndoWrist Surgical System, used in endoscopic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V795000·2019-11-06

    Blue Bird Recalls 2013-2020 Vision School Buses for Brake Light Defect

    Blue Bird is recalling 2013-2020 Vision school buses with Ford engines because brake lights may stay on continuously, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide