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.

33826–33850 of 73900

  • ModerateFDA (Devices)·Z-1387-2019·2019-05-29

    KaVo Recalls DEXIS Titanium Intraoral Sensors Due to Calibration Error

    KaVo Dental Technologies is recalling 211 DEXIS Titanium Intraoral Sensors because incorrectly programmed calibration files may reduce image quality.

    Product
    DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is intended to acquire dental intraoral radiographic images. The DEXIS / KaVo sensor shall be operated by healthcare professionals, who are educated and competent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1406-2019·2019-05-29

    Remel Thio Med w/Dex, Hem, Vit K Media Recalled for Performance Failure

    Remel Inc is recalling 1,069 units of Thio Med w/Dex, Hem, Vit K media due to potential performance failures after 106 days.

    Product
    Thio Med w/Dex, Hem, Vit K (10ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1370-2019·2019-05-29

    Cook Stent Sets Recalled for Missing Warning About Stent Knotting

    Cook Inc. is recalling Kwart RetroInject and Salle Intraoperative Pyeloplasty Stent Sets because the instructions for use did not include a warning for stent knotting.

    Product
    Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN: 4.0 Fr - SIPSF-040018-56-6 G18168 4.0 Fr - SIPSF-040018-59 G32773 4.7 Fr SIPSF-050018-59 G32774
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1380-2019·2019-05-29

    Remel Thio Med w/Dex, Hem, Vit, K Media Recalled for Performance Failure

    Remel Inc is recalling Thio Med w/Dex, Hem, Vit, K media because it may fail performance testing after 57 days. The expiration date is shortened to 56 days.

    Product
    Thio Med w/Dex, Hem, Vit, K (7ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1404-2019·2019-05-29

    Remel Thio Med Media Recalled for Potential Performance Failure

    Remel Inc is recalling Thio Med w/o Ind, w/Dex media because it may fail performance testing after 106 days. The expiration date is being shortened to 105 days.

    Product
    Thio Med w/o Ind, w/Dex (10ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1280-2019·2019-05-29

    Neusoft NeuViz 128 CT Scanner Recalled for Software Defect

    Neusoft Medical Systems is recalling six NeuViz 128 CT scanners due to a software defect that may cause image loss during specific scans.

    Product
    NeuViz 128 Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x-ray system featuring a continuously rotating x-ray tube and detector array. The acquired x-ray transmission data is reconstructed by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1279-2019·2019-05-29

    Neusoft NeuViz 64 CT Scanner Recalled for Image Loss Defect

    Neusoft Medical Systems is recalling 37 NeuViz 64 CT scanners due to a software defect that can cause image loss during specific scans.

    Product
    NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x-ray system featuring a continuously rotating x-ray tube and detector array. The acquired x-ray transmission data is reconstructed by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1408-2019·2019-05-29

    Remel Thio Med Culture Media Recalled for Potential Performance Failure

    Remel Inc is recalling Thio Med culture media due to potential performance failures after 106 days. The expiration date is shortened to 105 days.

    Product
    Thio Med w/o Ind, w/Dex (18ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1389-2019·2019-05-29

    Collagen Matrix Recalls Neomem Membrane Due to Incorrect Packaging

    Collagen Matrix, Inc. is recalling Neomem Resorbable Collagen Membranes because they were packaged in the wrong box, potentially inside a Neomem FLEXPLUS box.

    Product
    Neomem Resorbable Collagen Membrane, 15 mm x 20 mm Reference Number (model): N1520 - Product Usage: Neomem is a bioresorbable, implantable collagen material that is intended for use in dental surgery procedures as a material for placement in the area of dental implant, bone…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·060-2019·2019-05-28

    Richwell Group Recalls Frozen Siluriformes Fish Products for Import Violations

    Richwell Group is recalling 160,020 pounds of frozen fish products imported from Vietnam without proper inspection. No illnesses have been reported.

    Product
    Richwell Group, Inc. Recalls Siluriformes Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V393000·2019-05-24

    Blue Bird Recalls Buses Due to Rear Brake Dragging Risk

    Blue Bird is recalling certain 2015-2020 Vision and All American non-school buses because driver-side rear brakes may drag, posing a fire and injury risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V391000·2019-05-24

    Blue Bird Recalls School Buses Due to Rear Brake Dragging Risk

    Blue Bird is recalling 2015-2020 Vision and All American school buses because the driver-side rear brakes may drag, posing a fire and injury risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, ALL AMERICAN SCHOOL BUS, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V395000·2019-05-24

    Starcraft All Star XL Diesel Fuel Heater Fire Risk Recall

    Forest River is recalling 2018-2019 Starcraft All Star XL diesel vehicles because the fuel heater may overheat, melt plastic, and cause a fire or engine stall.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V392000·2019-05-24

    Land Rover Recalls Range Rover Models for Door Latch Defect

    Jaguar Land Rover is recalling 2013-2016 Range Rover and 2014-2016 Range Rover Sport vehicles because doors may appear closed but are unlatched, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E036000·2019-05-23

    Meritor recalls steer axles due to insufficient lubrication risk

    Meritor is recalling specific steer axles because insufficient lubrication may damage wheel end bearings, potentially causing wheel separation and loss of vehicle control.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E035000·2019-05-23

    Transfer Flow Recalls Rear Brake Lines for Mobility Van Conversions

    Transfer Flow is recalling rear brake lines for mobility van conversions due to incorrect tube nut fittings that may cause a pressure drop in the braking system.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V386000·2019-05-23

    BMW Recalls 2019 X7 Vehicles Due to Head Air Bag Alignment Defect

    BMW is recalling 2019 X7 xDrive40i and xDrive50i vehicles because the driver and passenger head air bags may not be properly aligned, potentially impairing deployment and increasing injury risk.

    Product
    BMW — BMW X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V387000·2019-05-23

    GM Recalls 2016-2019 Chevrolet Express and GMC Savana for Window Glass Defect

    General Motors is recalling 2016-2019 Chevrolet Express and GMC Savana vehicles because rear-quarter windows may use tempered glass instead of laminated glass, increasing injury risk in crashes.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V390000·2019-05-23

    Land Rover Recalls 2016 Range Rovers for Door Latch Defect

    Jaguar Land Rover is recalling 28,671 2016 Range Rover and Range Rover Sport vehicles because a stuck spring may leave the left door unlatched, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19127·2019-05-23

    DICK'S Sporting Goods Recalls Ethos Pull-Up Assist Due To Laceration Hazard

    DICK'S Sporting Goods is recalling Ethos Pull-Up Assist equipment because a plastic clip can break, posing a laceration hazard. Seven reports of equipment breaking resulted in six lacerations.

    Product
    Ethos Pull-Up Assist
    Category
    Consumer Product
    Distribution
    Distributed nationwide