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.

32376–32400 of 73900

  • SevereNHTSA·19V634000·2019-08-28

    2020 MINI Cooper and JCW Recalled for Missing Rear Crash Pads

    BMW is recalling 2020 MINI Cooper, Cooper S, and JCW vehicles because rear side trim panels may lack crash pads, increasing injury risk in side impacts.

    Product
    MINI — MINI JCW, COOPER, COOPER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V625000·2019-08-28

    Jayco Recalls 2019 Embark Motorhomes Due to Steering Shaft Bolt Issue

    Jayco is recalling 2019 Embark motorhomes because insufficiently tightened steering shaft bolts may allow the steering column to come loose, increasing crash risk.

    Product
    JAYCO — JAYCO EMBARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V628000·2019-08-28

    Jayco Eagle HT Fifth Wheel Trailers Recalled for Pin Box Bolt Defect

    Jayco is recalling 2019-2020 Eagle HT fifth wheel trailers because incorrect pin box bolts may allow the box to rotate in two places, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE HT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19190·2019-08-28

    Kirkland's Recalls Chests of Drawers Due to Tip-Over and Entrapment Hazards

    Kirkland's is recalling about 3,000 chests of drawers because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards.

    Product
    Black Wash Mirrored Chests and Six-Drawer Camille Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·19774·2019-08-28

    Yamaha Recalls Golf Cars and Specialty Vehicles Due to Fire Hazard

    Yamaha is recalling about 16,000 golf cars and specialty vehicles because a USB power module can overheat and melt, posing a fire hazard.

    Product
    Yamaha golf cars, personal transportation and specialty vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V631000·2019-08-28

    BMW Recalls 2020 X5 and X7 Models for Steering Rack Defect

    BMW is recalling 2020 X5 and X7 vehicles because steering rack pinion teeth may break, causing loss of steering control and increasing crash risk.

    Product
    BMW — BMW X5, X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V630000·2019-08-28

    Pierce Recalls 2019 Tanker Vehicles Due to Front Axle Lubrication Defect

    Pierce Manufacturing is recalling one 2019 Pierce Tanker vehicle because insufficient front axle lubrication may damage wheel end bearings, potentially causing wheel separation and loss of control.

    Product
    PIERCE — PIERCE TANKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E058000·2019-08-28

    ZF Recalls Steering Center Rods for 1996-2004 BMW 5 Series

    ZF North America is recalling aftermarket steering center rods for 1996-2004 BMW 5 Series vehicles due to a risk of detachment causing loss of steering control.

    Product
    BMW — BMW 5 SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2060-2019·2019-08-28

    Green Water Recalls Multiple Herbal Tinctures and Teas Due to Salmonella Risk

    Green Water, LLC is recalling specific lots of Taspen's Organics herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.

    Product
    Taspen s Organics, Bedroom Bliss Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2308-2019·2019-08-28

    BD Vacutainer Blood Collection Tubes Recalled for False COHb Results

    Becton Dickinson is recalling BD Vacutainer LH blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.

    Product
    BD Vacutainer LH (Lithium Heparin) 34 I.U. Plus Blood Collection Tubes, Catalog Number 368494
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2341-2019·2019-08-28

    Siemens N Cuvette Segments Recalled for Falsely Elevated Albumin Results

    Siemens Healthcare Diagnostics is recalling N Cuvette Segments for the BN ProSpec System because they may produce falsely elevated albumin results.

    Product
    N Cuvette Segments for BN ProSpec System-IVD a system for the quantitative determination of proteins in serum, plasma, urine and CSF. Siemens Material Number (SMN):10446539
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2310-2019·2019-08-28

    BD Vacutainer Lithium Heparin Tubes Recalled for False COHb Results

    Becton Dickinson is recalling BD Vacutainer LH blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.

    Product
    BD Vacutainer LH (Lithium Heparin) 102 I.U. Plus Blood Collection Tubes, Catalog Number 368886
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2066-2019·2019-08-28

    Green Water Recalls Taspens Organics Tea and Herbal Tinctures for Salmonella

    Green Water, LLC is recalling Taspens Organics tea and herbal tinctures due to potential Salmonella contamination. The products were distributed nationwide.

    Product
    Taspens Organics, Organic Tea: Mothers Milk, 2 ounce.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2349-2019·2019-08-28

    Thoratec Heartmate 3 Sealed Outflow Graft Recall for Leak Risk

    Thoratec Corp. is recalling 149 Heartmate 3 Sealed Outflow Graft units because the C-Ring may not seat properly, causing leaks during implantation.

    Product
    Thoratec Heartmate 3 Sealed Outflow Graft with Bend Relief, Sterile, REF 105581US/105581, RX only, Part of Left Ventricular Assist Device (LVAD) UDI: 00813024013266
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2294-2019·2019-08-28

    TiSport Recalls TiLite Wheelchair Anti-Tip Tubes for Tipping Risk

    TiSport is recalling 1,452 TiLite wheelchairs because the anti-tip tubes may fail, allowing the chair to tip backwards.

    Product
    TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-tip extension for manual wheelchairs). Product Usage: The affected component is part of a manual wheelchair to provide mobility to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2290-2019·2019-08-28

    Siemens IMMULITE 2000 Progesterone Test Recalled for Potential Low Results

    Siemens is recalling IMMULITE 2000 Progesterone tests because some samples may produce falsely low results, potentially leading to unnecessary medication.

    Product
    IMMULITE 2000 Progesterone; Models US: L2KPW2, L2KPW6 and OUS: L2KPW2(D), L2KPW6(D); SMN Numbers US: 10901873, 10901874 and OUS 10381181, 10381170
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2296-2019·2019-08-28

    BD Vacutainer Tubes Recalled for False Carboxyhemoglobin Results

    Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.

    Product
    BD Vacutainer Lithium HeparinN (LH) 37 USP Units Blood Collection Tubes, Catalog Number 366664
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2061-2019·2019-08-28

    Green Water Recalls Multiple Herbal Tinctures and Teas Due to Salmonella Risk

    Green Water, LLC is recalling several herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.

    Product
    Taspen s Organics, Breathe Easy Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2319-2019·2019-08-28

    Qiagen QIAsymphony SP Software 5.0.3 Recalled for Barcode Assignment Error

    Qiagen is recalling QIAsymphony SP software version 5.0.3 because it incorrectly assigns 2D barcode eluate IDs to samples, which could lead to incorrect patient reporting.

    Product
    QIAsymphony SP SOW 5.0.3, software used with the QIAsymphony SP Instrument (The QIAsymphony SP instrument is designed to perform automated purification of nucleic acids-IVD) Model Number: 9001297 Product Usage: The QIAsymphony SP instrument is designed to perform automated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2289-2019·2019-08-28

    Siemens IMMULITE 1000 Progesterone Test Recall for Low Results

    Siemens is recalling IMMULITE 1000 Progesterone tests because they may produce falsely low results, potentially leading to unnecessary progesterone supplementation.

    Product
    IMMULITE 1000 Progesterone, Model LKPW1, SMN Number 10381128
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2293-2019·2019-08-28

    DeRoyal Enteral Safe Feeding Tubes Recalled for Connector Detachment

    DeRoyal Industries is recalling specific polyurethane feeding tubes because the connector may detach from the tube.

    Product
    DeRoyal Enteral Safe Feeding Tubes: a) REF 54-2450R, 5 FR x 24" Polyurethane b) REF 54-2465R, 6.5 FR x 24" Polyurethane c) REF 54-2480R, 8 FR x 24" Polyurethane d) REF 54-3680R, 8 FR x 36" Polyurethane Product Usage: Feeding tube
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2292-2019·2019-08-28

    Luminex Aries M1 Barcode Scanner Recall for Sample Mismatch Risk

    Luminex is recalling Aries M1 barcode scanners due to incorrect control boards that could cause patient sample mismatches or duplicate results.

    Product
    Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 For In Vitro Diagnostic Use in clinical laboratories. Scanner Label/Labeling: JADAK JDK-2330 REV B 170512-017
    Category
    Medical Device
    Distribution
    Distributed nationwide