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.

Which agencies issued them

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.

31826–31850 of 73900

  • HighFDA (Devices)·Z-0039-2020·2019-10-16

    Aziyo BioEnvelope Surgical Mesh Recalled for Possible Suture Brittleness

    Aziyo Biologics is recalling BioEnvelope surgical mesh envelopes due to possible suture brittleness or breakage along the seam before the expiration date.

    Product
    BioEnvelope, surgical mesh envelope. Labeled as the following: 1. BioEnvelope (Medium) (single pack); 2. BioEnvelope (Large) (single pack); 3. BioEnvelope (Extra Large) (single pack); 4. BioEnvelope (Extra Extra Large) (single pack); 5. BioEnvelope…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0038-2020·2019-10-16

    Vital Scientific V-Twin Automated Chemistry Analyzer Recall for Cooling Defect

    Vital Scientific N.V. is recalling 192 V-Twin automated chemistry analyzers because an improperly installed cooling indicator board may prevent warning signals if reagent cooling fails.

    Product
    V-Twin, Catalog # 6002-800, UDI: 03661540600180 - Product Usage: An in vitro diagnostic device, which is an automated chemistry analyzer, micro type, intended for clinical use in conjunction with certain materials to measure a variety of analytes, including applications in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0101-2020·2019-10-16

    Centurion Medical Recalls VANTEX CVC Bundles Due to Connector Defect

    Centurion Medical Products is recalling VANTEX 7FR, 16CM, 3L CVC Bundles because the included BD MaxZeroNeedleess Connector may leak fluid droplets after disconnection.

    Product
    VANTEX 7FR, 16CM, 3L CVC BUNDLE ECVC6670
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0093-2020·2019-10-16

    Centurion Medical CVC Bundle Recall Due to Fluid Droplet Risk

    Centurion Medical is recalling CVC Bundle Multimeds containing a recalled BD connector due to potential fluid droplet separation.

    Product
    CVC BUNDLE MULTIMED, 3L, 20CM ECVC6060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0089-2020·2019-10-16

    Centurion Medical Recalls Central Venous Access Device Bundles

    Centurion Medical Products Corporation is recalling Central Venous Access Device Bundles because they include a connector recalled for potential fluid droplet separation.

    Product
    CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0102-2020·2019-10-16

    Centurion IV Start Kits Recalled Due to Fluid Droplet Risk

    Centurion Medical Products is recalling IV Start Kits containing a recalled BD connector due to potential fluid droplet separation.

    Product
    IV START KIT IV8440
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0057-2020·2019-10-16

    BD Microtainer Tubes Recalled for Damaged Reservoirs Causing Test Errors

    Becton Dickinson is recalling BD Microtainer Tubes with K2E because damaged reservoirs may cause insufficient sample volume and erroneous test results.

    Product
    BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0075-2020·2019-10-16

    Centurion PICC Line Accessory Kit Recalled for Fluid Droplet Risk

    Centurion Medical Products is recalling PICC Line Accessory Kits containing a BD connector that may release fluid droplets upon disconnection.

    Product
    PICC Line Accessory Kit CVI4285
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0104-2020·2019-10-16

    Centurion Medical Recalls Sorbaview IV Kits Due to Fluid Droplet Risk

    Centurion Medical Products Corporation is recalling Sorbaview IV kits because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.

    Product
    IV KIT - SORBAVIEW IVS3475
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0055-2020·2019-10-16

    BD Microtainer Tubes Recalled for Damaged Reservoirs and Erroneous Test Results

    Becton Dickinson is recalling specific lots of BD Microtainer Tubes with Lithium Heparin because damaged reservoirs may cause insufficient sample volumes and erroneous test results.

    Product
    BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0120-2020·2019-10-16

    Centurion Circlamp Recalled for Angle Mismatch Defect

    Centurion Medical Products is recalling 1,530 Circlamps due to a design mismatch that may cause the device to remove foreskin without a scalpel.

    Product
    Centurion CIRCLAMP W/1.1CM BELL - single-use, disposable instrument used to compress the foreskin of the penis during circumcision of a male infant. ReOrder: 310CR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0090-2020·2019-10-16

    Centurion Medical CVC Bundle Recall Due to Fluid Droplet Risk

    Centurion Medical Products is recalling CVC Bundles because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.

    Product
    CVC BUNDLE, 20CM, 4L, PI ECVC5095
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V739000·2019-10-16

    Hyundai Translead Recalls 2018-2019 Dry Van Trailers for Air Hose Defect

    Hyundai Translead is recalling 2018-2019 Dry Van Trailers because a beam clip may detach, allowing air hoses to drag on the ground and potentially leak air.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD DRY VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0085-2020·2019-10-16

    Centurion Medical Recalls Infusa Port Kits Due to Fluid Droplet Risk

    Centurion Medical Products Corporation is recalling Infusa Port Kits containing a specific connector due to the potential for fluid droplets to separate from the sealed surface.

    Product
    INFUSA PORT KIT DYNDC1840F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0088-2020·2019-10-16

    Centurion Triple Lumen Bundle Kit Recalled for Fluid Droplet Risk

    Centurion Medical Products is recalling Triple Lumen Bundle Kits because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.

    Product
    TRIPLE LUMEN BUNDLE KIT ECVC1540
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0083-2020·2019-10-16

    Centurion Medical Products Recalls CAP CHANGE KIT DYNDC1496B

    Centurion Medical Products is recalling CAP CHANGE KIT DYNDC1496B because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.

    Product
    CAP CHANGE KIT DYNDC1496B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0044-2020·2019-10-16

    Roche AssayTip/AssayCup Tray Recall for Abnormal Internal Structure

    Roche Diagnostics is recalling AssayTip/AssayCup Trays used on the cobas e 801 module due to abnormal internal structure that may lead to incorrect patient results.

    Product
    AssayTip/AssayCup Tray-used on the cobas e 801 module which is a part of the cobas c 8000 MODULAR Analyzer Series (IVD for in vitro determination of analytes in human body fluids) Catalog Number: 5694302001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0103-2020·2019-10-16

    Centurion IV Securement Kit Recall Due to Fluid Droplet Risk

    Centurion Medical Products is recalling IV Securement Kits containing a recalled BD connector due to the potential for fluid droplets to separate from the sealed surface.

    Product
    IV SECUREMENT KIT IVS3405
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0084-2020·2019-10-16

    Centurion Infusa Port Kit Recalled for Fluid Droplet Risk

    Centurion Medical Products is recalling Infusa Port Kits containing a recalled BD connector due to the potential for fluid droplets to separate from the sealed surface.

    Product
    INFUSA PORT KIT DYNDC1840E
    Category
    Medical Device
    Distribution
    Distributed nationwide