The Recall Desk

State

US Virgin Islands product recalls

73,824 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53751–53775 of 74002

  • HighFDA (Devices)·Z-1690-2015·2015-06-03

    Maquet Cardiovascular Recalls HLS/HIT Set Advanced Due to Blood Leakage Risk

    Maquet Cardiovascular is recalling HLS/HIT Set Advanced consoles because a potential issue could cause blood to leak from the gas outlet port.

    Product
    HLS/HIT Set Advanced with Bioline and/or Softline Coating Console Product Usage: HLS/HIT Set Advanced: The CARDIO HELP System in configuration with the HLS/HIT Set Advanced is intended to be used within the hospital environment and outside the hospital environment (for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1687-2015·2015-06-03

    Terumo Advanced Perfusion System 1 Recalled for Power Loss Risk

    Terumo is recalling 1,713 Advanced Perfusion System 1 units worldwide due to a risk of losing system power during critical medical procedures.

    Product
    100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1675-2015·2015-06-03

    Mindray Recalls Panorama Patient Monitoring Network Due to Software Anomaly

    Mindray is recalling four Panorama Patient Monitoring Network units due to a software anomaly that prevents arrhythmia alarms from displaying on the Panorama system after a restart.

    Product
    Panorama Patient Monitoring Network, Multi- Parameter Patient Monitor (with Arrhythmia Detection and Alarm. Part number 0998-00-0708-01. The Panorama Network includes the Panorama Telemetry System, which acquires and monitors physiological data for ambulating patients…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1669-2015·2015-06-03

    Siemens Luminos Agile Max Imaging System Software Recall

    Siemens is recalling 133 Luminos Agile Max imaging systems due to a software defect that causes image loss and connection issues.

    Product
    SIEMENS Luminos Agile Max; a universal imaging system for radiographic and fluoroscopic studies. Using either film cassettes or a digital mobile flat detector, it can perform a range of applications including general R/F, angiography and pediatric examinations. Luminos Agile is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1085-2015·2015-06-03

    Boehringer Ingelheim Roxane Recalls Subpotent Acarbose Tablets

    Boehringer Ingelheim Roxane Inc is recalling Acarbose 50 mg tablets because potency was below specification at a 9-month stability time point.

    Product
    ACARBOSE — ACARBOSE (ACARBOSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1668-2015·2015-06-03

    Siemens Axiom Luminos dRF Max Recall for Software Data Loss

    Siemens is recalling 133 Axiom Luminos dRF Max imaging systems due to a software defect that can cause acquired images to be deleted, requiring studies to be repeated.

    Product
    SIEMENS Axiom Luminos dRF Max, a universal diagnostic imaging system for radiographic and fluoroscopic studies. Using a digital flat detector, it can perform a range of applications including general R/F, angiography and pediatric examinations. The Axiom Luminos dRF is a device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1645-2015·2015-06-03

    Siemens SOMATOM Emotion 16 CT Scanner Software Recall

    Siemens is recalling 75 SOMATOM Emotion 16 CT scanners due to software bugs that may cause system crashes, image freezes, or database locks, potentially requiring patients to be rescanned.

    Product
    SOMATOM Emotion 16, the intended use of computed tomography is to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angels or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1644-2015·2015-06-03

    Siemens SOMATOM Emotion 6 CT Scanner Software Recall

    Siemens Medical Solutions is recalling 75 SOMATOM Emotion 6 CT scanners due to software bugs that may cause system crashes, image freezes, or database locks, potentially requiring patients to be rescanned.

    Product
    SOMATOM Emotion 6; the intended use of computed tomography is to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angels or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1667-2015·2015-06-03

    Siemens Ysio Max Radiographic System Recalled for Software Data Loss

    Siemens is recalling 133 Ysio Max radiographic systems because a software defect can delete acquired images and studies, requiring patients to repeat exposures.

    Product
    SIEMENS Ysio Max; a radiographic system used in hospitals, clinics, and medical practices. Ysio Max enables radiographic and tomographic exposures of the whole body including: skull, chest, abdomen, and extremities and may be used on pediatric, adult and bariatric patients. It…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1670-2015·2015-06-03

    Siemens Uroskop Omnia Max X-Ray System Software Data Loss Recall

    Siemens is recalling 133 Uroskop Omnia Max X-ray systems due to software defects that cause image deletion and connection issues.

    Product
    SIEMENS Uroskop Omnia Max ; a solid state detector fluoroscopic X-Ray system, primarily for urological applications (functional x-ray diagnostic, endourology and minimal invasive urology/surgery). The system,, which includes a radiologic/urologic treatment table, may be used for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1646-2015·2015-06-03

    Siemens SOMATOM Perspective CT Scanner Software Recall

    Siemens is recalling 75 SOMATOM Perspective CT scanners due to software bugs that may cause system crashes, image freezes, or database locks, potentially requiring patients to be rescanned.

    Product
    SOMATOM Perspective; the intended use of computed tomography is to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angels or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1676-2015·2015-06-03

    Biocare Medical Recalls D2-40 Lymphatic Marker Due to Incorrect Instructions

    Biocare Medical is recalling 19 units of D2-40 Lymphatic Marker because incorrect Instructions for Use were shipped with the product.

    Product
    D2-40 (Lymphatic Marker); For In Vitro Diagnostic; Catalog number: PM266AA Product Usage: In Vitro Diagnostic Use.: a mouse monoclonal antibody that is intended for laboratory use in the qualitative identification of O-linked sialoglyprotein protein by immunohistochemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1087-2015·2015-06-03

    Teva Recalls QVAR Inhalers Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling QVAR inhalers because stability testing revealed out-of-specification impurity results.

    Product
    QVAR (beclomethasone dipropionate HFA 40 mcg), 40 mcg Inhalation Aerosol, For Oral Inhalation with QVAR Actuator Only, 120 metered inhalations, Rx Only, Mktd by Teva Respiratory, LLC., Horsham, PA. mfd by 3M Drug Delivery Systems, Northridge, CA, NDC 59310-0202-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2323-2015·2015-06-03

    Ubervita Recalls W700 Lose Weight Supplement Due to Packaging Error

    Ubervita LLC is recalling less than 30 units of W700 Lose Weight Fast W700 Thermogenic Hyper-Metabolizer dietary supplements sold at Walmart due to a packaging error.

    Product
    UBERVITA LOSE WEIGHT FAST W700 THERMOGENIC HYPER-METABOLIZER DIETARY SUPPLEMENT. The product has an outer box which contains a labeled bottle. This is a bright red box with gold and chrome foil. Bottle inside is black and red in color. UPC 7 00115 35277 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V339000·2015-06-02

    Ford Recalls 2015 Mustangs for Fuel Leak and Fire Risk

    Ford is recalling 2015 Mustangs with 2.3L engines because heat can degrade fuel lines, causing leaks and fire risks.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V337000·2015-06-02

    Mitsubishi Recalls Eclipse Vehicles Due to ABS Valve Seizure Risk

    Mitsubishi is recalling 2006-2009 Eclipse and 2007-2009 Eclipse Spyder vehicles because corrosion in the ABS unit may cause valves to seize, reducing braking ability.

    Product
    MITSUBISHI — MITSUBISHI ECLIPSE SPYDER, ECLIPSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V336000·2015-06-02

    Airstream Interstate Motorhomes Recalled for Screen Door Exit Hazard

    Airstream is recalling 2015-2016 Interstate NCV3 B motorhomes because the screen door may prevent occupants from opening the sliding door to exit in an emergency.

    Product
    AIRSTREAM — AIRSTREAM INTERSTATE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V338000·2015-06-02

    Mitsubishi, Chrysler, and Dodge Recall Vehicles for Sun Visor Airbag Hazard

    Mitsubishi, Chrysler, and Dodge are recalling specific 2000-2005 vehicles because the passenger sun visor may detach during airbag deployment, increasing injury risk.

    Product
    CHRYSLER — CHRYSLER, DODGE, MITSUBISHI SEBRING, STRATUS, ECLIPSE, ECLIPSE SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V340000·2015-06-02

    Ford Recalls 2011-2013 Vehicles for Electric Power Steering Defect

    Ford is recalling specific 2011-2013 Ford, Lincoln, and Mercury vehicles because the electric power steering assist system may shut down, increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD, MERCURY MKZ, FUSION, MILAN, TAURUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15154·2015-06-02

    ORTOVOX S1+ Avalanche Transceiver Recalled for Signal Failure Risk

    CPSC recalls about 3,000 ORTOVOX S1+ avalanche transceivers because they may fail to transmit a signal during emergencies. Consumers should stop using them and return them for repair.

    Product
    ORTOVOX S1+ Avalanche Transceiver
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V335000·2015-06-01

    Porsche Recalls 2015 918 Spyder Vehicles Due to Fire Risk

    Porsche is recalling 223 model year 2015 918 Spyder vehicles because a wiring harness may chafe and cause an electrical short, increasing the risk of a fire.

    Product
    PORSCHE — PORSCHE 918 SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V331000·2015-06-01

    Van Hool Recalls Coaches Due to Front Steering Knuckle Breakage Risk

    Van Hool is recalling specific 2014-2015 coaches because the front steering knuckle carrier may break, potentially causing the wheel to separate and increasing crash risk.

    Product
    VAN HOOL — VAN HOOL TD925, TDX25, TX40, TX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V330000·2015-06-01

    Oshkosh Recalls S-Series Concrete Mixers Due to Engine Fire Risk

    Oshkosh is recalling 2012-2014 S-Series Front Discharge Concrete Mixers because excessive engine pressure may cause oil to leak onto hot surfaces, increasing fire risk.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide