The Recall Desk

State

US Virgin Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35526–35550 of 73915

  • SevereNHTSA·19V060000·2019-01-29

    Honda Recalls Acura and Honda Vehicles for Fuel Pump Defect

    Honda is recalling 2015-2019 Acura and Honda vehicles because fuel pump particulates may cause engine stalls, increasing crash risk.

    Product
    ACURA — ACURA, HONDA MDX, ACCORD, TLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V059000·2019-01-28

    Gillig Recalls 2016-2018 Low Floor Buses for Steering Defect

    Gillig is recalling 2016-2018 Low Floor buses because a steering draglink ball stud may not be properly tightened, increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V058000·2019-01-28

    Keystone Montana Recalled for Kitchen Slide Bolt Tire Contact Risk

    Keystone RV is recalling 2019 Montana trailers because a kitchen slide adjustment bolt may contact the tire, potentially causing tire failure and increasing crash risk.

    Product
    KEYSTONE — KEYSTONE MONTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V055000·2019-01-28

    Stoughton Recalls 2016-2019 DVW Trailers Due to Cracking Hitch Points

    Stoughton is recalling 2016-2019 DVW trailers because the forward attachment points for the pintle mounting assembly may crack, potentially causing the trailer to detach from the tow vehicle.

    Product
    STOUGHTON — STOUGHTON DVW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V057000·2019-01-28

    Audi Recalls 2013-2016 A8 and S8 Models for Fuel Leak Risk

    Volkswagen Group of America is recalling 2013-2016 Audi A8 and S8 vehicles because a fuel supply line may leak, increasing the risk of fire.

    Product
    AUDI — AUDI A8, S8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V020000·2019-01-24

    Ram 1500 Recall: Improperly Secured Battery Ground Fastener

    Chrysler is recalling 2019 Ram 1500 vehicles because an improperly secured battery ground fastener may cause loss of power steering assist, increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V054000·2019-01-24

    Mack Trucks Recalls 2019-2020 Models Due to Detaching Mirror Risk

    Mack Trucks is recalling 2019-2020 Anthem, Granite, and Pinnacle vehicles because the passenger-side door mirror may detach, posing a risk of injury or crash.

    Product
    MACK — MACK PINNACLE (PI/PN), PINNACLE (CHU), GRANITE (GR), ANTHEM (AN)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V052000·2019-01-24

    Acura Recalls 2014-2019 ILX Vehicles for Fuel Tank Defect

    Acura is recalling 2014-2019 ILX vehicles because a deformed fuel tank may cause the fuel gauge to display inaccurate levels, potentially leading to stalling and crashes.

    Product
    ACURA — ACURA ILX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V049000·2019-01-23

    Spartan K1 Motor Home Chassis Recalled for Brake Component Defect

    Spartan is recalling 2019-2020 K1 motor home chassis because missing or improper cotter pins may cause brake actuator rods to detach, increasing stopping distance.

    Product
    SPARTAN — SPARTAN K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0724-2019·2019-01-23

    Arthrex Suture Anchor Recall Due to Potential Breakage During Insertion

    Arthrex is recalling Nano Corkscrew FT Suture Anchors because they may break during insertion. The recall covers 1,418 units distributed in the US and abroad.

    Product
    Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with needles.) Part Number AR-1317FT Product Usage: Soft tissue fixation to bone in the hand and wrist
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0750-2019·2019-01-23

    Kimberly-Clark Recalls U by Kotex Sleek Tampons for Structural Defect

    Kimberly-Clark is recalling U by Kotex Sleek tampons because they may come apart upon removal. The recall covers 68,852,076 units distributed nationwide and in Canada.

    Product
    U by Kotex¿ Sleek¿, Regular/Super Tampons, 34 Count Multipack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0735-2019·2019-01-23

    Zimmer Biomet Recalls Maximum Variable Pitch Compression Screw Caddy

    Zimmer Biomet is recalling 971 Maximum Variable Pitch Compression Screw Caddies due to a potential for silicone shedding during cleaning and sterilization.

    Product
    Maximum Variable Pitch Compression Screw Caddy, Reference Number 231201003 Product Usage: Intended to carry implants and instruments during regular inventory distribution and handling and sterilization in the hospitals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0749-2019·2019-01-23

    U by Kotex Sleek Regular Tampons Recalled for Potential Breakage

    Kimberly-Clark is recalling U by Kotex Sleek Regular Tampons because they may come apart upon removal.

    Product
    U by Kotex¿ Sleek¿, Regular Tampons, 34 Count
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0734-2019·2019-01-23

    Zimmer Biomet Recalls Compression Tray Bases Due to Silicone Shedding

    Zimmer Biomet is recalling 971 Maximum Variable Pitch Compression Tray Bases because they may shed silicone during cleaning and sterilization.

    Product
    Maximum Variable Pitch Compression Tray Base, Reference Number 231201002 Product Usage: Intended to carry implants and instruments during regular inventory distribution and handling and sterilization in the hospitals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0732-2019·2019-01-23

    Meridian Premier Cryptococcal Antigen Test Recalled for Stability Issues

    Meridian Bioscience is recalling Premier Cryptococcal Antigen kits because an enzyme reagent may not maintain stability, potentially causing false negative results.

    Product
    PREMIER Cryptococcal Antigen, Catalog Number 602096 Product Usage: The PREMIER Cryptococcal Antigen enzyme immunoassay (EIA) is a screening or a semi-quantitative test system for the detection of capsular polysaccharide antigens of Cryptococcus neoformans in serum and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0733-2019·2019-01-23

    Waldemar Link LINK STEM Reconstruction Prosthesis Recalled for Depth Defect

    Waldemar Link is recalling 11 LINK STEM Reconstruction Prostheses because a manufacturing defect prevents the reaming guide from reaching the intended depth, which may lead to incorrect surgical positioning.

    Product
    LINK STEM with Microporous Surface MP Reconstruction Prosthesis, CEMENTLESS (Size XS-0, D: 12mm, L: 160mm), Reference Number 172-916/12 Product Usage: The LINK¿ STEM with Microporous Surface MP¿ Reconstruction Prosthesis, CEMENTLESS System is indicated for patients with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0745-2019·2019-01-23

    Bayer Medical Care Recalls MAVIG Portegra Overhead Counterpoise Systems

    Bayer Medical Care is recalling MAVIG Portegra and Portegra2 Overhead Counterpoise Systems because the head mount knob may not be properly tightened, causing the injector head to become loose or fall.

    Product
    MAVIG Portegra or Portegra2 Overhead Counterpoise System (OCS) used in conjunction with the Medrad Stellant CT Injection System (Certegra Workstation), Medrad Mark 7 Arterion" Injection System, or Medrad Mark V ProVis Injection System, Catalog Numbers: Catalog numbers: OCS CEIL…
    Category
    Medical Device
    Distribution
    Distributed nationwide