The Recall Desk

State

US Virgin Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52551–52575 of 73995

  • HighNHTSA·15V549000·2015-09-01

    Spartan Motorhomes Recalled for Potential Engine Cooling Fan Separation

    Spartan Motors USA is recalling 2004-2008 K2, K3, and MM motorhomes because the engine cooling fan may separate from the drive, posing an injury risk to nearby individuals.

    Product
    SPARTAN — SPARTAN MM, K3, K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15228·2015-09-01

    MiWorld Recalls iPhone Wall Chargers Due to Fire Hazard

    MiWorld Accessories is recalling iPhone 5/5S wall chargers sold at Charlotte Russe because they can overheat and catch fire. One fire incident was reported.

    Product
    USB Cord & Wall Chargers for iPhone 5/5S
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V550000·2015-09-01

    Kawasaki Recalls Vulcan 1700 Motorcycles for Ignition Wire Chafing Risk

    Kawasaki is recalling specific Vulcan 1700 Voyager and Vaquero motorcycles because an ignition wire may chafe against the fuel tank, causing a short circuit and potential engine stall.

    Product
    KAWASAKI — KAWASAKI VULCAN 1700 VOYAGER, VULCAN 1700 VAQUERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·117-2015·2015-08-31

    Ocho Rios Recalls Canned Corned Beef Lacking Import Inspection

    Ocho Rios is recalling approximately 7,228 pounds of canned corned beef imported from Brazil that was not presented for U.S. inspection. No adverse reactions have been reported.

    Product
    Ocho Rios Recalls Corned Beef Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V546000·2015-08-31

    Mitsubishi Recalls Lancer Models Due to Fuel Tank Fire Risk

    Mitsubishi is recalling 2014-2015 Lancer Evolution and Ralliart vehicles because a parking brake cable may wear the fuel tank coating, increasing fire risk.

    Product
    MITSUBISHI — MITSUBISHI LANCER EVOLUTION, LANCER RALLIART
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V544000·2015-08-31

    Micro Bird Recalls 2013-2015 G5 Transit Buses for Battery Fire Risk

    Micro Bird is recalling 2013-2015 G5 transit buses because corroded battery studs may cause short circuits and fires, or missing bolts may cause battery detachment.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·118-2015·2015-08-31

    Holten Meat Recalls Beef Patties Due to Unlabeled MSG

    Holten Meat Inc. is recalling approximately 501,509 pounds of Extra Value Meats Quarter Pound Beef Patties because monosodium glutamate (MSG) was used but not listed on the label.

    Product
    Branding Iron Holdings - Holten Meat — Recall Notification Report 118-2015 (Beef Patties)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V543000·2015-08-27

    Strick Van Trailers Recalled for Weak Rear Impact Guards

    Strick Trailers is recalling 2001 and 2009 Van Trailers because rear impact guards may be too weak to prevent vehicles from sliding underneath during a crash.

    Product
    STRICK — STRICK VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E069000·2015-08-27

    Alpine Audio Amplifiers Recalled for Overheating Circuit Board Fire Risk

    Alpine Electronics is recalling specific audio amplifiers because a manufacturing error may cause the power circuit board to overheat, increasing the risk of a vehicle fire.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E070000·2015-08-27

    Holley Recalls Nitrous Oxide Systems Due to Valve Fracture Risk

    Holley is recalling NOS-brand Nitrous Oxide systems manufactured between May and August 2015 because solenoid valves may fracture under pressure, posing an injury risk.

    Product
    FUEL SYSTEM, OTHER:FUEL INJECTION SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15221·2015-08-27

    Huffy Recalls Bicycles with Front Disc Brakes Due to Crash Hazard

    Huffy is recalling about 460 model year 2014 TR 745 and TR-S 740 bicycles because an open quick release lever can contact the front disc brake, causing a crash.

    Product
    Huffy bicycles equipped with front disc brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15750·2015-08-27

    Tippmann Recalls Paintball Markers Due to Trigger Safety Failure

    Tippmann Sports is recalling about 6,500 rental paintball markers because the trigger safety can fail, allowing paintballs to fire unexpectedly. No injuries have been reported.

    Product
    Paintball Markers (Guns)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·115-2015·2015-08-27

    Swanson Recalls Boneless Beef Tender Tips Due to Undeclared Allergens

    Swanson Meats is recalling approximately 20,063 pounds of boneless beef tender tips because the labels failed to declare soybean oil, MSG, and papain.

    Product
    Swanson Meat Co. — Recall Notification Report 115-2015 (Boneless Beef Tender Tips)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2367-2015·2015-08-26

    Teleflex Medical Recalls Sheridan Sher-I-BRONCH Endobronchial Tubes

    Teleflex Medical is recalling Sheridan Sher-I-BRONCH endobronchial tubes because the double swivel connector may crack or separate.

    Product
    HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Left sided), Sizes: 28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr., Rx Only, Sterile. Intended for use in thoracic surgery, bronchospirometry, for the administration of bronchial anesthesia and other uses commonly requiring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1333-2015·2015-08-26

    Mylan Recalls Gemcitabine Injection Vials Due to Particulate Matter

    Mylan Institutional LLC is recalling 2,455 vials of Gemcitabine for Injection due to the presence of particulate matter.

    Product
    Gemcitabine for Injection, USP, 2 g*/vial, Lyophilized powder in a Single-Use Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103, Made in India, NDC 67457-463-02, UPC 3 67457 46302 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2372-2015·2015-08-26

    Elite Biomedical Recalls Alaris Medley LVP Bezel Assemblies

    Elite Biomedical Solutions LLC is recalling 346 Alaris Medley LVP Bezel Assemblies used in infusion pumps due to a risk of administering inappropriate fluid quantities.

    Product
    Alaris Medley LVP Bezel Assembly. Intended use to hold platen assembly and help protect the bezel assembly's internal components from fluid intrusion. This part is used in the Alaris Medley LVP 8100 infusion pump.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2329-2015·2015-08-26

    FDA Recalls 657 Puritan Bennett 980 Ventilators Due to Volume Defects

    The FDA is recalling 657 Puritan Bennett 980 Ventilators because tidal volumes may be lower than set in neonatal mode, potentially causing respiratory compromise.

    Product
    Puritan Bennett 980 Ventilator System, Universal (with neonatal functionality enabled) and Neonatal Models. Designed for use on Neonatal (NICU) through Adult patient populations who require respiratory support or mechanical ventilation and weigh a minimum of 0.3 kg (0.66 lb).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2343-2015·2015-08-26

    Draeger Evita Infinity V500 Ventilator Battery Recall

    Draeger Medical is recalling 2,081 Evita Infinity V500 ventilators because the optional PS500 battery capacity did not last as long as expected.

    Product
    PS500 of an IACS Workstation Critical Care (Evita Infinity V500); intended for the ventilation of adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2399-2015·2015-08-26

    Winco Designer Care Cliner Recalled for Non-Fire Retardant Foam

    Winco Mfg. is recalling Designer Care Cliner chairs because the foam used was not fire retardant as required.

    Product
    Winco Designer Care Cliner w/Swing Arms - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2371-2015·2015-08-26

    Elite Biomedical Recalls Alaris Medley LVP Frame Membranes

    Elite Biomedical Solutions LLC is recalling 609 Alaris Medley LVP Frame Membranes because the defect could allow fluid intrusion, potentially leading to injury or death.

    Product
    Alaris Medley LVP Frame Membrane. Intended use to hold platen assembly and help protect the bezel assembly's internal components from fluid intrusion. This part is used in the Alaris Medley LVP 8100 infusion pump.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1334-2015·2015-08-26

    Mylan Recalls Gemcitabine for Injection Due to Particulate Matter

    Mylan Institutional LLC is recalling 10,094 vials of Gemcitabine for Injection due to the presence of particulate matter.

    Product
    Gemcitabine for Injection, USP, 1 g*/vial, Lyophilized powder in a Single-Use Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103, Made in India, NDC 67457-462-01, UPC 3 67457 46201 1.
    Category
    Drug
    Distribution
    Distributed nationwide