The Recall Desk

State

US Virgin Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44651–44675 of 73984

  • SevereNHTSA·17V057000·2017-01-26

    GM Recalls 2016-2017 Chevrolet Cruze for Seat-Back Welding Defect

    General Motors is recalling 2016-2017 Chevrolet Cruze vehicles because a defective weld in the seat-back recliner mechanism may cause the seat to break in a crash, increasing injury risk.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V059000·2017-01-26

    Forest River Recalls 2017-2018 Berkshire and Charleston RVs for Fire Risk

    Forest River is recalling 2017-2018 Berkshire and Charleston RVs because a power steering hose may rub a power stud, causing arcing and fluid leaks that increase fire risk.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE, CHARLESTON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V062000·2017-01-26

    BMW Recalls 2016-2017 X1 Vehicles for Passenger Air Bag Defect

    BMW is recalling 2016-2017 X1 vehicles because the instrument panel may prevent the front passenger air bag from deploying properly, increasing injury risk in a crash.

    Product
    BMW — BMW X1 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V056000·2017-01-26

    Jayco Recalls 2017 Eagle Fifth-Wheel Trailers Due to Propane Leak Risk

    Jayco is recalling 2017 Eagle fifth-wheel recreational vehicles with the dry camping option because the LP manifold can crack, causing a propane gas leak and increasing fire risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V061000·2017-01-26

    GM Recalls Pontiac Solstice and Saturn Sky for Air Bag Sensor Defect

    General Motors is recalling 2006-2010 Pontiac Solstice and 2007-2010 Saturn Sky vehicles because a bent passenger air bag sensor may prevent the air bag from deploying in a crash.

    Product
    PONTIAC — PONTIAC, SATURN SOLSTICE, SKY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V060000·2017-01-26

    Forest River Recalls 2017 XLR Fifth-Wheel RVs for Incorrect Placard

    Forest River is recalling 2017 XLR fifth-wheel recreational vehicles because the Federal Placard incorrectly identifies them as Travel Trailers, which may lead to improper towing and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E008000·2017-01-26

    Triumph Recalls S 4 Alarm Kits Due to Battery Leak Risk

    Triumph is recalling S 4 Alarm Kits and Immobilizers because a leaking battery may cause the engine to stall, increasing crash risk.

    Product
    ELECTRICAL SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E007000·2017-01-25

    Porsche Recalls Replacement Engines Due to Fuel Leak Fire Risk

    Porsche is recalling specific replacement gasoline engines because screws may shear off, causing a fuel leak that increases the risk of fire.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:GASOLINE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0970-2017·2017-01-25

    Bard Halo One Introducer Sheath Recalled for Separation and Kinking

    Bard Peripheral Vascular is recalling Halo One 5F Introducer Sheaths due to complaints of sheath separation, kinking, and tip damage during use.

    Product
    Halo One 5F Introducer Sheath 10 cm 5 pack Product Code: HAL510F Product Usage: The Halo One Thin-Walled Guiding Sheath is designed to perform as both a guiding sheath and introducer sheath. The Halo One Thin-Walled Guiding Sheath is indicated for use in peripheral arterial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0977-2017·2017-01-25

    BioMerieux NucliSENS magnetic extraction reagents recalled for performance drift

    BioMerieux SA is recalling NucliSENS magnetic extraction reagents because a performance drift was observed in BK virus testing for certain silica batches.

    Product
    NucliSENS magnetic extraction reagents, For in vitro diagnostic use, Product Usage: NucliSENS miniMAG¿ is intended to be used for the extraction of total nucleic acids from biological specimens.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V054000·2017-01-25

    Porsche Recalls 2017 Models Due to Fuel Leak Fire Risk

    Porsche is recalling 2017 911 and 718 models because fuel collection pipe screws may shear, causing a fuel leak that increases fire risk.

    Product
    PORSCHE — PORSCHE 718 BOXSTER, 911 CARRERA, 911 TARGA 4, 718 CAYMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17073·2017-01-25

    Country Home Products Recalls Field and Brush Mowers for Fire Hazards

    Country Home Products is recalling about 830 DR brand field and brush mowers because a fuel tank valve malfunction can cause gasoline release, posing fire and burn risks.

    Product
    Field & brush mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V055000·2017-01-25

    Advance Engineered Recalls 2014-2015 Dry Bulk Cargo Tank Trailers

    Advance Engineered is recalling 2014-2015 Dry Bulk Cargo Tank trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    ADVANCE ENGINEERED — ADVANCE ENGINEERED DRY BULK CARGO TANK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1026-2017·2017-01-25

    Fresenius 2008T Hemodialysis System Recalled for Software Error

    Fresenius Medical Care is recalling 2008T Series Hemodialysis Systems because a software error may cause the machine to execute a cancelled ultrafiltration rate instead of the displayed rate.

    Product
    Fresenius 2008T Series Hemodialysis System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0950-2017·2017-01-25

    CareFusion Recalls Alaris Pump Modules Due to False Air-in-Line Alarms

    CareFusion is recalling Alaris Pump Modules and AIL sensor kits because false Air-in-Line alarms can interrupt medication infusions.

    Product
    Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221. The Alaris Pump module is a large volume infusion pump offered under the Alaris System. The Alaris Pump module will deliver medication and fluids using IV administration sets for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0969-2017·2017-01-25

    Bard Halo One Introducer Sheath Recalled for Separation and Kinking

    Bard Peripheral Vascular is recalling Halo One 5F Introducer Sheaths due to reports of sheath separation, kinking, and tip damage during use.

    Product
    Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Product Usage: The Halo One Thin-Walled Guiding Sheath is designed to perform as both a guiding sheath and introducer sheath. The Halo One Thin-Walled Guiding Sheath is indicated for use in peripheral arterial and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0968-2017·2017-01-25

    Bard Halo One Introducer Sheath Recalled for Separation and Kinking

    Bard Peripheral Vascular is recalling Halo One 5F Introducer Sheaths due to complaints of separation, kinking, and tip damage during use.

    Product
    Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 The Halo One Thin-Walled Guiding Sheath is designed to perform as both a guiding sheathand introducer sheath. The Halo One Thin-Walled Guiding Sheath is indicated for use inperipheral arterial and venous procedures…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1027-2017·2017-01-25

    Fresenius 2008K Hemodialysis System Recalled for Software Error

    Fresenius Medical Care is recalling 2008K Series Hemodialysis Systems because a software error may cause the machine to execute a cancelled Ultrafiltration Rate setting.

    Product
    Fresenius 2008K Series : Hemodialysis System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0976-2017·2017-01-25

    BioMerieux Recalls MagSIL Magnetic Silica Reagents Due to Performance Drift

    BioMerieux SA is recalling 3,723 units of MagSIL (NucliSENS easyMAG Magnetic Silica) worldwide due to observed performance drift in BK virus testing.

    Product
    MagSIL (NucliSENS easyMAG Magnetic Silica), Product Usage: The NucliSENS¿ easyMAG¿ system is an in vitro diagnostic medical device and is intended for the automated isolation (purification and concentration) of total nucleic acids (RNA/DNA) from biological specimens.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1029-2017·2017-01-25

    Fresenius 2008K@home Hemodialysis System Recalled for Software Defect

    Fresenius Medical Care is recalling 2008K@home hemodialysis systems because a software error may cause the machine to execute a cancelled ultrafiltration rate.

    Product
    Fresenius 2008K@home Series : Hemodialysis System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1018-2017·2017-01-25

    Binding Site Optilite Analyser Recalled for Lid Injury Risk

    The Binding Site Group is recalling 129 Optilite Analyser units because the lid may fall suddenly and cause injury if not fully open.

    Product
    Optilite Analyser, Product Code: IE700 Product Usage: The Thermo Scientific Indiko Clinical Chemistry Analyzer is a fully automated random access analyzer used to measure a variety of analytes that may be adaptable to the analyzer depending on the reagent used. The Indiko…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1263-2017·2017-01-25

    Herr Foods Recalls Smoked Chipotle Potato Chips Due to Salmonella Risk

    Herr Foods is recalling Smoked Chipotle Flavored Kettle Cooked Potato Chips because the seasoning contains a milk ingredient with a potential risk of Salmonella contamination.

    Product
    Smoked Chipotle Flavored Kettle Cooked Potato Chips 2.625 oz and 8.0 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1053-2017·2017-01-25

    Freelite Human Lambda Free Kit Recalled for Calibration Curve Error

    The Binding Site Group is recalling Freelite Human Lambda Free Kits due to a calibration curve change that causes an increase in false prozone flags.

    Product
    Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S, LK018.10S Freelite aids the detection and monitoring of Multiple Myeloma and related diseases
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1046-2017·2017-01-25

    Merge Cardio software recalled for potential image loading errors

    Merge Healthcare is recalling Merge Cardio software versions 9.0 through 10.1.2 because a specific user action may cause images to be missing, potentially leading to incorrect diagnosis or treatment.

    Product
    Merge Cardio software. Product Usage: Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files…
    Category
    Medical Device
    Distribution
    Distributed nationwide