The Recall Desk

State

US Virgin Islands product recalls

73,187 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.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14251–14275 of 73364

  • HighFDA (Devices)·Z-2582-2023·2023-09-20

    ACUSON Redwood 2.0 Ultrasound Systems Display Incorrect Measurement Results

    ACUSON Redwood 2.0 ultrasound systems may display underestimated measurement results when using an 18L6 transducer in Dual format, potentially leading to patient misdiagnosis. 796 units are affected worldwide.

    Product
    ACUSON Redwood 2.0 ultrasound systems, REF: 11503314
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1514-2023·2023-09-20

    Knorr Pasta Soup Mix recalled for undeclared egg allergen

    Conopco (Unilever) recalled Knorr Estrellitas con Tomate soup mix nationwide due to undeclared egg allergen. No illnesses have been reported.

    Product
    Knorr Estrellitas con Tomate Tomato Based Star Pasta Soup Mix 3.5 oz UPC: 048001716193
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2588-2023·2023-09-20

    FILMARRAY GI Panel Software Recalled for False Positive Cryptosporidium Results

    BioFire Diagnostics is recalling FILMARRAY Gastrointestinal Panel software due to an increased risk of false positive Cryptosporidium test results. Approximately 61,069 devices were distributed in the US and internationally.

    Product
    FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software
    Category
    Medical Device
    Distribution
    54 states
  • HighFDA (Devices)·Z-2524-2023·2023-09-20

    Medtronic Bone Graft Recalled Due to Incorrect Size Labeling

    Medtronic Sofamor Danek USA Inc is recalling Magnifuse Bone Graft products due to incorrect size labeling on 55 pouches. Units with specific serial numbers were distributed in nine U.S. states.

    Product
    Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V643000·2023-09-20

    Tiffin motorhomes recalled for cooktop electrical shock hazard

    Tiffin is recalling certain 2016-2024 Allegro Bus and 2017-2024 Zephyr motorhomes because the 240-volt cooktop may not be grounded, creating an electrical shock hazard. Tiffin will install a ground for the junction box at no charge.

    Product
    TIFFIN — TIFFIN ALLEGRO BUS, ZEPHYR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V674000·2023-09-20

    GM Recalls 2014 Buick Verano and Chevrolet Cruze for Air Bag Defect

    General Motors is recalling 2014 Buick Verano and Chevrolet Cruze vehicles because side roof-rail air bag inflators may rupture, potentially causing injury from metal fragments.

    Product
    CHEVROLET — CHEVROLET, BUICK CRUZE, VERANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1505-2023·2023-09-20

    Twin City Foods Frozen Corn Recalled for Listeria Contamination Risk

    Multiple frozen corn products distributed nationwide are being recalled due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.

    Product
    Kernel Corn, BEST PRICE TOPVALU, net wt. per bag 300g. Label is in foreign language. UPC 4549414086232 Signature Select Golden Corn Super Sweet, Product of USA, net wt. per bag 12oz, 12 bags per case. UPC 21130090655 Food Lion Super Sweet Cut Yellow Corn, Product of USA, net…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V644000·2023-09-20

    BMW Recalls 2023 740i, 760i, and i7 Models for Wiper Failure

    BMW is recalling 2023 740i, 760i, and i7 vehicles because windshield wipers may fail in certain weather, reducing visibility and increasing crash risk.

    Product
    BMW — BMW 740I, 760I, I7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1515-2023·2023-09-20

    Knorr Soup Mix Recalled for Undeclared Egg Allergen

    Conopco is recalling Knorr Fideos con Tomate Tomato Based Pasta Soup Mix because it contains undeclared egg. The product was distributed nationwide with best-by dates through July 6, 2024.

    Product
    Knorr Fideos con Tomate Tomato Based Pasta Soup Mix 3.5 oz UPC: 048001716162
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2578-2023·2023-09-20

    Medical Device Recall: ACL TOP Coagulation Analyzers for Sample Misidentification

    Instrumentation Laboratory is recalling ACL TOP coagulation analyzers due to potential sample misidentification that could result in incorrect test results and alter patient management decisions.

    Product
    ACL TOP Family 50 Series Models as follows: In vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis (1) ACL TOP 550 CTS Model…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V646000·2023-09-20

    Wabash National Dry Van Trailers Recalled for Rear Impact Guard Defect

    Wabash National is recalling certain 2009-2024 dry van trailers because the rear impact guard is positioned too far forward, potentially reducing crash protection. Dealers will add an extension to the guard free of charge.

    Product
    WABASH NATIONAL — WABASH NATIONAL VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2531-2023·2023-09-20

    Remel Todd Hewitt Broth Culture Medium May Fail to Detect Target Organism

    One lot of Remel Todd Hewitt Broth culture medium may fail to recover Group B Streptococci during testing or use with patient samples, potentially resulting in missed diagnoses.

    Product
    remel TODD HEWITT W. CNA (LIM BROTH), REF R064810; used to isolate Group B Streptococci form clinical specimens containing mixed bacterial flora
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1503-2023·2023-09-20

    Twin City Foods Frozen Corn Recalled Nationwide for Listeria Risk

    Twin City Foods recalled frozen corn products due to potential Listeria monocytogenes contamination. Products distributed nationwide and internationally.

    Product
    Individually Quick Frozen (IQF) Corn distributed in BULK TOTES (1650lbs and 1750lbs) to consignees for further processing. Bulk tote labels have cooking instructions. Individually Quick Frozen (IQF) Super Sweet Corn, foodservice item, packaged in 32oz. plastic bag, 12 bags per…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1506-2023·2023-09-20

    Mixed Vegetables Recalled for Potential Listeria monocytogenes Contamination

    Twin City Foods is recalling mixed vegetable products sold under TopValu, Food Lion, and Kroger brands due to potential Listeria monocytogenes contamination. Products were distributed in the US and internationally.

    Product
    Mixed Vegetables BEST PRICE TOPVALU, net per bag 500g. Label is in foreign language. 4549414484120 Food Lion Mixed Vegetables Carrots, Corn, Green Beans & Peas. Product of USA, net wt. per bag 16oz, 12 bags per case. Distributed by Food Lion, LLC Salisbury, NC. UPC 35826005090…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2577-2023·2023-09-20

    BeamAdjust software generates incorrect calibration files for radiation detectors

    BeamAdjust software Version 2.3.3 generates incorrect calibration files when using TIFF or DICOM image reference data, affecting radiation measurement accuracy in OCTAVIUS Detector systems.

    Product
    BeamAdjust software Version 2.3.3 Ref: S080032 The following devices are affected when a relative calibration is performed using ArrayCal (module from BeamAdjust S080032, UDI-DI: EPTWS0800320 ): " OCTAVIUS Detector 1600 SRS (T10056) (UDI-DI: EPTWT100560) " OCTAVIUS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1504-2023·2023-09-20

    Frozen Corn Recalled Due to Listeria monocytogenes Contamination

    Twin City Foods frozen corn in bulk cases is recalled nationwide due to potential Listeria monocytogenes contamination. Products were distributed to food processors in the United States, Costa Rica, China, and Japan.

    Product
    Individually Quick Frozen (IQF) Corn, distributed in bulk cases (1kg, 10kg, 12kg, 15kg, 25kg) to consignees for further processing. Cases are read in parts: Product of U.S.A. Packed By Twin City Foods, Inc. Stanwood, Washington. Super Sweet Grade A Cut Corn Blanched…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1149-2023·2023-09-20

    Prescription Drug Sucralfate Suspension Recalled for Out-of-Specification Potency

    VistaPharm LLC is recalling Sucralfate Oral Suspension 1g/10mL due to out-of-specification assay results. The active ingredient concentration does not meet FDA specifications in approximately 14,400 affected bottles distributed nationwide.

    Product
    SUCRALFATE — SUCRALFATE (SUCRALFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2581-2023·2023-09-20

    Welch Allyn Connex Spot Monitor Recalled for Improper Copper Tape Placement

    Baxter Healthcare is recalling the Welch Allyn Connex Spot Monitor due to improper placement of copper tape on the back of the liquid-crystal display. The device was distributed in California.

    Product
    Welch Allyn Connex Spot Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2579-2023·2023-09-20

    Copaliner Cavity Varnish Recalled for Solvent Mislabeling Error

    Keystone Industries recalls Copaliner Cavity Varnish after discovering bottles of Copaliner Solvent were accidentally packaged in boxes labeled as varnish. The error affected 337 units distributed worldwide.

    Product
    Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to provide a marginal seal between the dentin and amalgam which helps to protect against penetration of amalgam into the dentina Item No. 0921526
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2580-2023·2023-09-20

    Denture relining kit recalled for outer box labeling error

    Keystone Industries is recalling 240 units of Henry Schein Hard Line Chairside Reline kits because the outer box is labeled as Soft Line, though the contents and instructions are correctly labeled.

    Product
    Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture Relining Material KI Item No.: 0921940HS Henry Schein Item No.: 570-0718
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2576-2023·2023-09-20

    Microbiologics KWIK-STIK ANA quality control set missing strain

    Microbiologics Inc is recalling one lot of KWIK-STIK ANA QC sets missing one of three bacterial strains required for microbiological testing.

    Product
    KWIK-STIK, ANA (3 Strains) QC Set, REF 5065P; Microbiological testing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E068000·2023-09-18

    Hyundam Fuel Pump Recall for Potential Loss of Drive Power

    Hyundam Industrial is recalling fuel pumps where the impeller may deform, causing pump failure and loss of drive power, which increases the risk of a crash.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V641000·2023-09-18

    Jeep Wrangler and Gladiator reverse lights and camera failure recall

    Certain 2022-2023 Jeep Wrangler and Gladiator vehicles with manual transmission have a defective gear position sensor that may prevent the rearview camera from displaying and the reverse lights from illuminating, creating a visibility and safety hazard.

    Product
    JEEP — JEEP GLADIATOR, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E069000·2023-09-18

    Chrysler Recalls Mopar Gear Position Sensors and Transmission Assemblies

    Chrysler is recalling specific Mopar Gear Position Sensors and Transmission Assemblies because they may cause rearview camera and reverse light failures, increasing crash risk.

    Product
    POWER TRAIN:MANUAL TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V640000·2023-09-18

    2023 Dodge Durango Shifter Interference Can Cause Sudden Power Loss

    Chrysler is recalling certain 2023 Dodge Durango Pursuit vehicles because the shifter may slip out of gear while driving, causing sudden loss of drive power and increasing crash risk.

    Product
    DODGE — DODGE DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide