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.

35951–35975 of 73915

  • SevereNHTSA·18V840000·2018-11-27

    Mercedes-Benz Recalls 2019 GLC 300 for Steering Assist Failure

    Mercedes-Benz is recalling 2019 GLC 300 vehicles because a steering sensor may fail, deactivating power assist and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V833000·2018-11-27

    Lamborghini Recalls Gallardo Vehicles Due to Software Warning Failure

    Lamborghini is recalling 2011-2014 Gallardo vehicles because engine software may erase trouble codes, preventing warning lamps from illuminating for safety system failures.

    Product
    LAMBORGHINI — LAMBORGHINI GALLARDO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E107000·2018-11-27

    Wanda Recalls Aftermarket Windshields for 2014-2018 Toyota Highlanders

    Fujian Wanda is recalling aftermarket replacement windshields for 2014-2018 Toyota Highlanders because water leaks into the wire harness, potentially damaging the Engine Control Module and causing the engine to stall.

    Product
    TOYOTA — TOYOTA HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V838000·2018-11-27

    Mercedes-Benz Recalls 2018-2019 Models for Passenger Air Bag Display Error

    Mercedes-Benz is recalling specific 2018-2019 C-Class and GLC-Class vehicles because the passenger air bag status may display incorrectly, potentially leaving occupants unaware the air bag is off.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C 300, AMG GLC63S, C 350 E, C 300 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V832000·2018-11-26

    Airstream Recalls 2019 Interstate Motorhomes Due to Fuse Defect

    Airstream is recalling 2019 Interstate motorhomes because incorrect fuses may allow battery cables to overheat, increasing fire risk.

    Product
    AIRSTREAM — AIRSTREAM INTERSTATE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V830000·2018-11-26

    BMW Recalls One 2019 F850GS Motorcycle for Engine Defect

    BMW is recalling one 2019 F850GS motorcycle because engine connecting rods may be loose, risking engine damage and loss of power.

    Product
    BMW — BMW F850GS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V831000·2018-11-26

    Maserati Recalls 2014-2015 Models for Fuel Line Fire Risk

    Maserati is recalling 2014-2015 Quattroporte and Ghibli vehicles because damaged fuel lines may leak, increasing the risk of a fire.

    Product
    MASERATI — MASERATI QUATTROPORTE, GHIBLI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V824000·2018-11-26

    Volkswagen Recalls 2018-2019 Models for Missing Ignition Key Warning

    Volkswagen is recalling 2018-2019 Atlas, Tiguan, and Jetta vehicles because the instrument cluster may fail to provide an audible warning when the key is left in the ignition.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN, JETTA, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V829000·2018-11-26

    Nova Bus Recalls 2013-2018 LFS Artic Buses for Software Fault

    Nova Bus is recalling 2013-2018 LFS Artic transit buses because a software fault may cause the vehicle to operate at zero velocity and lack dampening, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V828000·2018-11-26

    Alfa Romeo Giulia Recall: Brake Fluid Leak Fire Risk

    FCA US LLC is recalling 2017-2018 Alfa Romeo Giulia AWD vehicles because brake fluid may leak onto the exhaust, increasing fire risk.

    Product
    ALFA ROMEO — ALFA ROMEO GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·117-2018·2018-11-23

    Chunwei Inc. Recalls Meat and Poultry Products Due to Misbranding and Undeclared Allergens

    Chunwei, Inc. is recalling meat and poultry products because they are misbranded and may contain undeclared allergens and MSG, with no confirmed illness reports.

    Product
    Chunwei, Inc. Recalls Meat and Poultry Products Due to Misbranding and Undeclared Allergens and Monosodium Glutamate
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·18V827000·2018-11-22

    New Flyer Bus Recall for Fire Extinguisher Actuator Defect

    New Flyer is recalling certain 2013-2017 buses because a fire extinguisher actuator may fail, preventing the suppression system from discharging during a fire.

    Product
    NEW FLYER — NEW FLYER XN60, XN40, XD40, XDE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0288-2019·2018-11-21

    Euphoric Male Performance Enhancer Recalled for Undeclared Prescription Drugs

    Epic Products, LLC is recalling Euphoric Premium Male Performance Enhancer capsules because they contain undeclared sildenafil, tadalafil, and oxytetracycline.

    Product
    Euphoric Premium Male Performance Enhancer capsules, packaged in a)1-count blister cards, UPC 6 96859 28646 9, b) 3-count bottle, UPC 6 96859 28647 6 and c) 12-count bottle, UPC 6 96859 28648 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0261-2019·2018-11-21

    Sandoz Recalls Isosorbide Dinitrate Tablets Due to Cross Contamination

    Sandoz Inc. is recalling 1,550 bottles of Isosorbide Dinitrate Tablets 20 mg due to cross-contamination with other products.

    Product
    Isosorbide Dinitrate Tablets, USP 20 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-222-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0246-2019·2018-11-21

    Zero Xtreme Dietary Supplement Recalled for Undeclared Sibutramine

    Zero Xtreme USA is recalling 16 bottles of Zero Xtreme Dietary Supplement capsules because they contain undeclared sibutramine and were marketed without an approved NDA or ANDA.

    Product
    Zero Xtreme Dietary Supplement 30-count capsules. By:Zero Xtreme Registro Sanitario No SD2014-0002208 LLC-USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0448-2019·2018-11-21

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus Hip Fracture Nail Left 125 Deg 11x300mm, Item Number 814411300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0413-2019·2018-11-21

    GE Healthcare Recalls Aisys Anesthesia System Touchscreen Display Kits

    GE Healthcare is recalling 4,207 Aisys anesthesia system touchscreen display kits because they fail to transition to backup ventilation if a patient stops breathing.

    Product
    Touchscreen display kit. Sold under the following product names: TOUCHSCREEN DISPLAY KIT 11.X ENGLISH FOR USA, TOUCHSCREEN DISPLAY KIT 11.X ENGLISH, TOUCHSCREEN DISPLAY KIT 11.X GERMAN, TOUCHSCREEN DISPLAY KIT 11.X DUTCH, TOUCHSCREEN DISPLAY KIT 11.X FRENCH, TOUCHSCREEN…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V826000·2018-11-21

    Navistar Recalls 2018-2019 International Trucks for Clutch Assembly Defect

    Navistar is recalling certain 2018-2019 International trucks because a clutch component may fail, causing unintended vehicle movement and increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL RH, MV, LONESTAR, HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0259-2019·2018-11-21

    Sandoz Recalls Isosorbide Dinitrate Tablets Due to Cross Contamination

    Sandoz Inc. is recalling Isosorbide Dinitrate Tablets 5 mg due to cross-contamination with other products. The recall affects 7,817 bottles distributed nationwide.

    Product
    Isosorbide Dinitrate Tablets, USP 5 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-223-00
    Category
    Drug
    Distribution
    Distributed nationwide