The Recall Desk

State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42901–42925 of 73919

  • LowNHTSA·17V387000·2017-06-20

    KZRV Recalls 2018 Recreational Trailers Due to Missing Certification Date

    KZRV is recalling 2018 recreational trailers because the Federal Certification label lacks the manufacturing date, potentially preventing owners from identifying other safety recalls.

    Product
    KZRV — KZRV VENOM, SPORTSMEN SPORTSTER, SPREE, SPORT TREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V386000·2017-06-19

    BYD Recalls 2015-2016 K7 M Buses for Wiper Arm Defect

    BYD is recalling 2015-2016 K7 M buses because wiper arms may crack and detach, reducing visibility and increasing crash risk.

    Product
    BYD — BYD K7 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V385000·2017-06-19

    Starcraft RV Recalls 2018 Launch Outfitter Trailers for Electrical Outlet Defect

    Starcraft RV is recalling 2018 Launch Outfitter travel trailers because an electrical outlet lacks Ground Fault Circuit Interrupter protection, increasing the risk of electrical shock.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT LAUNCH OUTFITTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·075-2017·2017-06-17

    Supreme Cuisine Recalls Meat and Poultry Fat Products Due to Processing Deviation

    Supreme Cuisine is recalling approximately 325,000 pounds of meat and poultry fat and lard products due to a processing deviation that may allow bacterial pathogens to grow.

    Product
    Supreme Cuisine Recalls Meat and Poultry Fat and Lard Products Due to Processing Deviation
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17750·2017-06-16

    Advanced Composites Recalls Bicycle Forks Due to Fall Hazard

    Advanced Composites is recalling about 40 Wound Up Tandem Duo Disc bicycle forks because the fork leg can crack, posing a fall hazard.

    Product
    Bicycle forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V381000·2017-06-15

    Thor Motor Coach Recalls 2018 Outlaw 29H Motorhomes for Fire Risk

    Thor Motor Coach is recalling 2018 Outlaw 29H motorhomes because an incorrect fuse size may increase the risk of a fire if the awning light circuit short circuits.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH OUTLAW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V382000·2017-06-15

    GM Recalls 2014-2016 Chevrolet SS Vehicles for Steering Defect

    General Motors is recalling 2014-2016 Chevrolet SS vehicles because corrosion may cause a loss of electric power steering assist, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2283-2017·2017-06-14

    Arrow VPS Access Kit Recalled for Needlestick Injury Risk

    Arrow International is recalling VPS Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    Arrow¿ VPS¿ Access Kit with Maximal Barrier Precautions for use with 4 Fr. Peripherally Inserted Central Venous Catheter The intended use of the VPS Stylet and Console (VPS System) is to quickly and accurately guide market available peripherally inserted central catheters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2225-2017·2017-06-14

    Magellan LeadCare Blood Lead Test Kits Recalled for Underestimating Results

    Magellan Diagnostics is recalling LeadCare and LeadCare II test kits because they may underestimate lead concentrations in venous blood samples.

    Product
    Magellan Diagnostics LeadCare and LeadCare II test Kits. Product Usage: The LeadCare Blood Lead Test Kit is for in vitro diagnostic use only. The Test Kit is for the quantitative measurement of lead in fresh whole blood. This product is for professional use only. Sensors…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2246-2017·2017-06-14

    Baxter MiniCap PD Transfer Set Recalled for Connection Leak Risk

    Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets because connection issues may cause leaks and contamination, potentially leading to peritonitis.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short. 1 Unit. Sterile. Baxter Healthcare Corporation, Deerfield, IL 60015 USA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2253-2017·2017-06-14

    Arrow International Recalls Central Venous Access Kits Due to Needlestick Risk

    Arrow International is recalling MAC Two-Lumen Central Venous Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue(R) Access Device, Integral Hemostasis Valve, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters The MAC(TM) Multi-Lumen Central Venous Access Device with ARROWg+ard Blue(R)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2299-2017·2017-06-14

    Arrow Arterial Catheterization Kits Recalled for Needlestick Injury Risk

    Arrow International is recalling Arterial Catheterization Kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.

    Product
    Arterial Catheterization Kit with Maximal Barrier Precautions The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V378000·2017-06-14

    Newmar Recalls 2012-2015 Motorhomes Due to Starter Motor Fire Risk

    Newmar is recalling 2012-2015 King Aire and Essex motorhomes because a starter motor component may break, causing overheating and increasing the risk of a fire.

    Product
    NEWMAR — NEWMAR KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2265-2017·2017-06-14

    Arrow International Recalls Large-Bore CVC Kits Due to Needlestick Risk

    Arrow International is recalling 43,394 units of ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kits nationwide due to safety cover disengagement and needlestick injury risks associated with packaged BD Eclipse Needles.

    Product
    ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit The large-bore multiple-lumen catheter permits venous access to the central circulation for rapid fluid administration
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2259-2017·2017-06-14

    Arrow International Recalls Central Venous Access Kits Due to Needlestick Risk

    Arrow International is recalling 43,394 units of MAC Two-Lumen Central Venous Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue (R) Access Device, Integral Hemostasis Valve, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 -8 Fr. Catheters. The MAC(TM) Multi-Lumen Central Venous Access Device with ARROWg+ard Blue(R)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2281-2017·2017-06-14

    Arrow VPS Access Kit Recalled Due to Needlestick Injury Risk

    Arrow International is recalling VPS Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Inserted Central Venous Catheter The intended use of the VPS Stylet and Console (VPS System) is to quickly and accurately guide market available peripherally inserted central catheters (PICCs) to the goal location which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2268-2017·2017-06-14

    Arrow Pressure Injectable PICC Kit Recalled for Needlestick Injury Risk

    Arrow International is recalling 43,394 units of Pressure Injectable PICC Kits due to safety cover disengagement and needlestick injury reports.

    Product
    Arrow Pressure Injectable PICC Kit The Arrow International Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central venous system for intravenous therapy and blood sampling.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2279-2017·2017-06-14

    Arrow International Recalls CVC Kits Due to Needlestick Injury Risk

    Arrow International is recalling specific CVC kits because the packaged BD Eclipse Needle may disengage, posing a needlestick injury risk to medical personnel.

    Product
    AGB+ Pressure Injectable Multi-Lumen CVC Kit The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.The ARROWg+ard Blue¿ Catheter permits venous access to the central circulation by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2275-2017·2017-06-14

    Arrow Central Venous Catheter Kits Recalled for Needlestick Injury Risk

    Arrow International is recalling specific central venous catheter kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.

    Product
    Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter The ARROWg+ard Blue Plus" antimicrobial catheter is indicated in the short-term ( < 30 days) treatment of diseases or conditions requiring central venous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2278-2017·2017-06-14

    Arrow International Recalls Multi-Lumen CVC Kits Due to Needlestick Risk

    Arrow International is recalling specific multi-lumen central venous catheter kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    AGB+ Pressure Injectable Multi-Lumen CVC Kit intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins
    Category
    Medical Device
    Distribution
    Distributed nationwide