The Recall Desk

State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53401–53425 of 74002

  • HighNHTSA·15V434000·2015-07-07

    Fleetwood Southwind Recalled for Missing Emergency Exit Window

    Allied Recreation Group is recalling 2015-2016 Fleetwood Southwind RVs because some may lack a required emergency exit window on the road side bedroom wall.

    Product
    FLEETWOOD — FLEETWOOD SOUTHWIND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V429000·2015-07-06

    Entegra Recalls 2015-2016 Cornerstone Motorhomes Due to Brake Hose Rubbing

    Entegra is recalling 2015-2016 Cornerstone motorhomes because rear jack plates may rub against the brake air hose, potentially reducing braking performance and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V428000·2015-07-06

    Prevost Recalls 2015 X3-45 Coaches Due to Front Hub Carrier Defect

    Prevost is recalling 68 model year 2015 X3-45 Commuter Coaches because front hub carriers may leak or crack, potentially causing loss of vehicle control.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V426000·2015-07-06

    Mercedes-Benz Recalls 2014 CLA Models Due to Fuse Installation Error

    Mercedes-Benz is recalling 2014 CLA 250 and CLA 45 AMG vehicles because incorrectly installed fuses may cause airbag and instrument cluster failures.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLA250, AMG CLA45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V427000·2015-07-06

    Harley-Davidson Recalls 2014-2015 Motorcycles Due to Saddlebag Mounting Defect

    Harley-Davidson is recalling approximately 185,272 model year 2014-2015 motorcycles because saddlebag mounting receptacles may not adequately secure the saddlebags, creating a road hazard.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHXSE, FLHP, FLHR, FLHTCU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V425000·2015-07-06

    Thomas Built Buses Recall Emergency Door Handle Corrosion Defect

    Daimler Trucks North America is recalling certain Thomas Built Buses because corrosion on the emergency door handle stem may delay evacuation during an emergency.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES, THOMAS SAF-T-LINER HDX, SAF-T-LINER C2, SAF-T-LINER CONVENTIONAL, SAF-T-LINER FS65
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V423000·2015-07-02

    Terex Advance Recalls 2015 Concrete Mixer Trucks Due to Drum Bolt Issue

    Terex Advance is recalling 120 model year 2015 Front Discharge Concrete Mixer Trucks because improperly tightened bolts may allow the mixing drum to separate, increasing crash risk.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE CONCRETE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E057000·2015-07-02

    Norco Accu Slide Room Mechanism Recall for Unintentional Extension

    Norco is recalling Accu Slide room mechanisms where screws may fail, allowing the room to extend while driving and increasing crash risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E055000·2015-07-02

    Osram Sealed Beam Headlamps Recalled for Insufficient Illumination

    Osram is recalling specific Sealed Beam Headlamps that may not meet federal intensity requirements, potentially causing crashes due to poor visibility.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1820-2015·2015-07-01

    Hill-Rom Steriseal-Cannula Ophthalmic Recall Due to Dislodgement Risk

    Hill-Rom is recalling Steriseal-Cannula Ophthalmic handpieces because the metal cannula can rotate and become dislodged from the plastic handpiece.

    Product
    Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2737-3015·2015-07-01

    Natural Grocers Raw Macadamia Nuts Recalled for Salmonella Contamination Risk

    Vitamin Cottage Natural Food Markets is recalling specific lots of Natural Grocers Raw Macadamia Nuts due to potential Salmonella contamination.

    Product
    Natural Grocers Raw Macadamia Nuts, Net Wt. 10 oz. package, Sealed plastic bag.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2773-2015·2015-07-01

    Mi Costenita Bocadin Wafers Recalled for Undeclared Milk Allergen

    Yoli, Inc. is recalling Mi Costenita Bocadin chocolate-covered wafers due to undeclared milk allergens. The product was distributed nationwide in 26 states.

    Product
    Chocolate covered wafers (Bocadin) in plastic packaging sold under the Mi Costenita brand and packaged and distributed by Yoli, Inc.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V420000·2015-07-01

    Gillig Recalls 2010-2015 Low Floor Buses Due to Fire Risk

    Gillig is recalling 2010-2015 Low Floor transit buses because a power cable may chafe a fuel line, increasing fire risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1835-2015·2015-07-01

    Stryker Recalls Optical Access Systems Due to Fracture Risk

    Stryker is recalling specific Optical Access Systems because they may fracture at the tip, leaving fragments at the surgical site.

    Product
    Optical Access System; 5mm x 100mm and 12mm x 100mm; Model #: CTR03 and CTR73. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1834-2015·2015-07-01

    Stryker Recalls Fios First Entry Trocars Due to Fracture Risk

    Stryker is recalling Fios First Entry trocars because some may fracture at the distal tip, leaving fragments at the surgical site.

    Product
    Fios First Entry; 5mm x 100mm and 12mm x 100mm; Model #:CTF03 and CTF73. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V418000·2015-07-01

    Nissan Recalls Juke, Cube, Versa for Sticking Start/Stop Button

    Nissan is recalling 2013-2014 Juke, Cube, and 2014 Versa vehicles because the engine start/stop button may stick, potentially causing the engine to shut off while driving.

    Product
    NISSAN — NISSAN JUKE, CUBE, VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1831-2015·2015-07-01

    Stryker Recalls SERFAS 90 Degree Energy Probes Due to Fragmentation

    Stryker Endoscopy is recalling 22,063 SERFAS 90 degree Energy Probes because fragments of the probe have been reported to break off into patients during arthroscopic procedures.

    Product
    SERFAS 90 degree Energy Probe, Part Number 279-350-101; SERFAS Energy Probes are indicated for arthroscopic procedures of the knee, shoulder, ankle, hip, elbow and wrist. Specifically, the probes are used for resection, ablation and coagulation of soft tissue, as well as the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1809-2015·2015-07-01

    Teleflex Recalls Lifesaver Manual Resuscitators Due to Potential Intake Port Blockage

    Teleflex Medical is recalling 9,333 units of Lifesaver Single Patient Use Manual Resuscitators because the intake port may be blocked, causing the bag to fail to fill.

    Product
    Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual resuscitator with pressure monitoring port is a disposable medical device intended for use on patients requiring temporary augmentation of ventilation with or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1836-2015·2015-07-01

    Stryker Recalls Trocars Due to Reported Fracture at Distal Tip

    Stryker is recalling specific cannula and seal models because they may fracture at the tip, leaving fragments at the surgical site.

    Product
    Cannula and Seal; 5mm x 100mm and 12mm x 100mm Model #: CTS02 and CTS22. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1827-2015·2015-07-01

    Fresenius NaturaLyte Liquid Bicarbonate Concentrate Recalled for Bacterial Contamination

    Fresenius Medical Care is recalling NaturaLyte Liquid Bicarbonate Concentrate due to bacterial contamination. The product is used in hemodialysis machines.

    Product
    NaturaLyte Liquid Bicarbonate Concentrate (Dialysate Concentrate for Hemodialysis (liquid), 6.4 Liter Bottle Catalog Number: 08-4000-LB This concentrate is formulated to be used with a three steam hemodialysis machine which is calibrated for acid and bicarbonate concentrates.
    Category
    Medical Device
    Distribution
    Distributed nationwide