The Recall Desk

State

US Virgin Islands product recalls

73,809 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47576–47600 of 73987

  • ModerateFDA (Devices)·Z-2256-2016·2016-07-27

    Siemens ADVIA Centaur XPT Software Recalled for Potential Result Errors

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur XPT system software versions V1.0.1 through V1.1 due to eight identified issues that may affect test results.

    Product
    ADVIA¿ Centaur XPT system software versions V1.0.1 (Bundle 1.0.912 SMN 10819704), V1.0.2 (Bundle 1.0.1086 SMN 11219806), V1.0.3 (Bundle 1.0.1108 SMN 11220781) and V1.1 (Bundle 1.1.243 SMN 11221979). Product Usage: This system is intended for professional use in a laboratory…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2225-2016·2016-07-27

    WalkMed Recalls IV Administration Sets Due to Potential Particulate Presence

    WalkMed Infusion is voluntarily recalling specific IV administration sets due to the potential presence of particulate matter in or on the devices.

    Product
    T090-000W 90" 20 Drop IV Admin Set w/2 Needlefree Y-Sites Back Check Valve. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2220-2016·2016-07-27

    WalkMed Infusion Pumps Recalled for Unapproved Software and Specification Changes

    WalkMed Infusion is recalling Triton and Triton FP infusion pumps due to unapproved changes to software, specifications, and intended use.

    Product
    The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1705-2016·2016-07-27

    Bolthouse Farms Recalls Protein Plus Drinks Due to Spoilage

    Bolthouse Farms is recalling eight varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.

    Product
    Bolthouse Farms Strawberry Protein Plus: 30 g protein per bottle + 21 vitamins & minerals. Packaged in 15.2 oz/450 mL item number: PPCN4BF6; 32 oz/946 mL. - item number PPSWQBF6 Selling Unit UPC Case GTIN 15.2 oz.…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2214-2016·2016-07-27

    DePuy Synthes Recalls TFNA Blade/Screw Guide Sleeves Due to Sizing Defect

    DePuy Synthes is voluntarily recalling TFNA Blade/Screw Guide Sleeves because a manufacturing defect may prevent proper use, potentially causing surgical delays.

    Product
    Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part Number ID 03.037.017, Class I exempt Lot Numbers: 9066399; 9066435; 9409790; 9519308; 9620447; 9301183; 9409792; 9519303; 9641077; 9301184; 9409791; 9542998…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1446-2016·2016-07-27

    Sun Pharmaceutical Recalls Bupropion Hydrochloride Tablets for Dissolution Failure

    Sun Pharmaceutical Industries is recalling 16,085 bottles of Bupropion Hydrochloride Extended Release Tablets because they failed dissolution specifications.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V558000·2016-07-26

    Forest River Recalls 2011-2016 Glaval Titan II Buses for Frame Cracks

    Forest River is recalling 39 Glaval Titan II Low Floor buses due to frames that may crack, potentially reducing driver control and increasing crash risk.

    Product
    GLAVAL BUS — GLAVAL BUS TITAN II LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V559000·2016-07-26

    2015 RAM 2500 and 3500 Recalled for Steering Bracket Weld Defect

    Chrysler is recalling 2015 RAM 2500 and 3500 trucks because inadequate welds on front track bar brackets may separate, reducing steering response and increasing crash risk.

    Product
    RAM — RAM 2500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V557000·2016-07-26

    Load Trail Triple Axle Tilt Deck Trailers Recalled for Weld Defects

    Load Trail is recalling 2014-2016 Triple Axle Tilt Deck trailers because weld joints may crack, potentially causing equipment to disengage and increasing crash risk.

    Product
    LOAD TRAIL — LOAD TRAIL TRIPLE AXLE TILT DECK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16759·2016-07-26

    Electrolux Recalls Frigidaire and Kenmore Wall Ovens Due to Fire Hazard

    Electrolux is recalling about 1,000 Frigidaire and Kenmore electric wall ovens because a malfunctioning thermal switch poses a fire hazard. No injuries have been reported.

    Product
    Electric wall ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16760·2016-07-26

    Inovonics Recalls Emergency Transmitters and Receivers Due to Signal Failure

    Inovonics is recalling about 5,500 emergency transmitters and receivers because they may fail to send or receive help signals. No injuries have been reported.

    Product
    Inovonics pendant transmitters, universal transmitters and add-on receivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E065000·2016-07-25

    ZF Transmission Sensor Clusters Recalled for Unexpected Neutral Shifts

    ZF North America is recalling certain 9-speed automatic transmission sensor clusters due to insufficient wire harness crimps that may cause the vehicle to unexpectedly shift to neutral.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION:CONTROL MODULE (TCM/PCM/TECM) recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V553000·2016-07-25

    BMW Recalls 2016-2017 MINI Clubman for Side Air Bag Defect

    BMW is recalling 2016-2017 MINI Clubman vehicles because side curtain air bags may not deploy correctly in a crash, increasing injury risk.

    Product
    MINI — MINI CLUBMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V550000·2016-07-22

    2017 Coachmen Freedom Express Recalled for Tire Rubbing Hazard

    Forest River is recalling 2017 Coachmen Freedom Express recreational vehicles because insufficient space between the driveshaft and tires may cause tire failure and loss of control.

    Product
    COACHMEN — COACHMEN FREEDOM EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V548000·2016-07-22

    Mitsubishi Outlander Sport Recall for CVT Hose Clamp Defect

    Mitsubishi is recalling 2015 Outlander Sport vehicles because a CVT hose clamp may not be secured, risking fluid leaks, inoperability, or fire.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V551000·2016-07-22

    Pierce Fire Apparatus Recall for Hydraulic Pump Plug Defect

    Pierce is recalling 2015-2016 Impel, Enforcer, and Velocity vehicles equipped with aerial devices because a plastic plug may separate, causing a hydraulic leak that disables the device.

    Product
    PIERCE — PIERCE IMPEL, ENFORCER, VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V547000·2016-07-22

    Forest River Surveyor Recalled for Incorrect Federal Placard Classification

    Forest River is recalling 2016-2017 Surveyor recreational trailers because the Federal Placard incorrectly classifies them as school buses, posing a crash risk due to potential overloading.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·063-2016·2016-07-22

    House of Smoke Recalls Wild Boar Brotwurst Due to High Nitrite Levels

    House of Smoke is recalling approximately 4,692 pounds of Wild Boar Brotwurst because nitrite levels exceeded regulatory limits. No adverse reactions have been reported.

    Product
    House Of Smoke, Inc. — House of Smoke Recalls Products Due To Nitrite Levels in Excess of Regulatory Limit
    Category
    Food
    Distribution
    Distributed nationwide