The Recall Desk

State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58301–58325 of 74005

  • SevereNHTSA·14V337000·2014-06-06

    Micro Bird Recalls G5 School Buses Due to Propane Leak Risk

    Micro Bird is recalling 2011-2013 G5 school buses with Roush propane systems because a metal reaction may cause a fuel leak, increasing fire risk.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V300000·2014-06-06

    GM Recalls 2012 Vehicles for Driver Air Bag Deployment Failure

    General Motors is recalling specific 2012 Buick Verano, Chevrolet Cruze, Sonic, and Camaro vehicles because the driver's air bag may fail to deploy in a crash.

    Product
    CHEVROLET — CHEVROLET, BUICK CRUZE, SONIC, CAMARO, VERANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V298000·2014-06-06

    GM Recalls 2013 Buick Encore and Chevrolet Spark for Air Bag Defect

    General Motors is recalling specific 2013 Buick Encore and Chevrolet Spark vehicles because an improper weld may prevent the passenger air bag from deploying, increasing injury risk.

    Product
    CHEVROLET — CHEVROLET, BUICK SPARK, ENCORE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V301000·2014-06-06

    GM Recalls 2014-2015 Trucks and SUVs for Radio Software Defect

    General Motors is recalling specific 2014-2015 Chevrolet and GMC vehicles because a radio software defect may disable audible safety warnings for open doors and unbuckled seat belts.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO, TAHOE, SIERRA, SIERRA HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V305000·2014-06-05

    KTM Recalls 2014 690 Enduro R Motorcycles Due to Rear Brake Pedal Defect

    KTM is recalling 649 model year 2014 690 Enduro R motorcycles because the rear brake pedal mounting bolt may loosen, allowing the pedal to detach and increasing crash risk.

    Product
    KTM — KTM 690 ENDURO R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1970-2014·2014-06-04

    Organic Traditions Dark Chocolate Recalled for Undeclared Milk Allergen

    Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Golden Berries because the product contains undeclared milk, a major food allergen.

    Product
    Organic traditions DARK CHOCOLATE GOLDEN BERRIES***DAIRY & SUGAR FREE 80% DARK CHOCOLATE; Pack sizes 3.5oz/100g, UPC 8 54260 00263 8; 5.3 oz (150g), UPC 8 54260 00266 9; 12kg bulk boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V296000·2014-06-04

    NABI Recalls 2012 31LFW Buses Due to Steering Column Weld Defect

    NABI is recalling 39 model year 2012 31LFW city transit buses because the steering column support bracket may not be properly welded, potentially causing steering failure.

    Product
    NABI — NABI 31LFW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V293000·2014-06-04

    Chrysler Recalls 2014 Vehicles for Adaptive Cruise Control Acceleration Defect

    Chrysler is recalling 2014 Dodge Durango, Jeep Cherokee, and Grand Cherokee vehicles because the adaptive cruise control system may cause unintended continued acceleration after the driver releases the pedal.

    Product
    DODGE — DODGE, JEEP DURANGO, CHEROKEE, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V295000·2014-06-04

    Ameritrail Recalls 2011 Ranch King Trailers Due to Brake Actuator Defect

    Ameritrail is recalling specific 2011 Ranch King trailers because a defective hydraulic pump component may cause a loss of braking ability, increasing the risk of a crash.

    Product
    RANCH KING — RANCH KING GN36-25D42, MFDD36-242, GN40-21D42, GN24-21E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V307000·2014-06-04

    Tactical Recalls Modified Ford F-350 and F-550 Trucks Due to Fire Risk

    Tactical Vehicle Outfitters is recalling modified 2010-2014 Ford F-350 and F-550 trucks because oil leaks from the PTO pressure switch may ignite the exhaust thermal blanket.

    Product
    FORD — FORD F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1971-2014·2014-06-04

    Organic Traditions Dark Chocolate Sacha Inchi Seeds Recalled for Undeclared Milk

    Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Sacha Inchi Seeds because the product contains undeclared milk, a major food allergen.

    Product
    Organic traditions DARK CHOCOLATE SACHA INCHI SEEDS***DAIRY & SUGAR FREE 80% DARK CHOCOLATE; Pack sizes: 3.5oz/100g, UPC 8 54260 00709 1; 5.3 oz (150g), UPC 8 54260 00718 3; 12kg bulk boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·14735·2014-06-04

    Lea Bunk Beds Recalled Due to Entrapment Hazard

    Lea Industries is recalling Covington and Hannah Collection bunk beds because incorrect assembly can create a space that traps young children.

    Product
    Lea Covington and Hannah Collection Bunk Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1660-2014·2014-06-04

    Physio-Control Recalls LIFEPAK 1000 Defibrillators Due to Unexpected Shutdowns

    Physio-Control is recalling 96,611 LIFEPAK 1000 defibrillators because a software malfunction can cause the device to shut down unexpectedly, potentially failing to deliver a life-saving shock.

    Product
    LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000 (in AED mode) is indicated for use on patients in cardiac arrest.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1672-2014·2014-06-04

    Abbott Recalls ARCHITECT Intact PTH Controls Due to Performance Shift

    Abbott is recalling ARCHITECT Intact PTH Controls because a performance shift may cause falsely elevated results on patient samples.

    Product
    ARCHITECT Intact PTH Controls consists of 3 x 1 Bottle (8.0 mL each) of PTH (synthetic peptide) in Bis Tris Propane buffer with protein (bovine) stabilizer. Preservatives: sodium azide and ProClin 300. Product Usage: The ARCHITECT Intact PTH assay is an in vitro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1979-2014·2014-06-04

    Dr. Mercola Organic Cocoa Cassava Bars Recalled for Undeclared Milk

    Mercola Group is voluntarily recalling Dr. Mercola Organic Cocoa Cassava bars because they may contain undeclared milk protein.

    Product
    Organic Cocoa Cassava bars, 1.59 oz (45 g), individually packaged in foil pouches and sold under the Dr. Mercola brand. Sold at retail locations in display cases containing 12 bars per display case. 12 display cases are packaged in each master case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·14V304000·2014-06-04

    Van Hool Recalls TX40 and TX45 Motorcoaches for Seat Belt Defect

    Van Hool is recalling 2014-2015 TX40 and TX45 motorcoaches because the driver seat belt may not be properly secured, increasing injury risk in a crash.

    Product
    VAN HOOL — VAN HOOL TX40, TX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1671-2014·2014-06-04

    Abbott Recalls ARCHITECT Intact PTH Calibrators Due to Performance Shift

    Abbott Laboratories is recalling 7,780 kits of ARCHITECT Intact PTH Calibrators because a performance shift may cause falsely elevated patient results.

    Product
    ARCHITECT Intact PTH Calibrators consists of 6 bottles (4.0 mL each). Calibrator A contains Bis Tris Propane buffer with protein (bovine) stabilizer. Calibrators B-F contain PTH (synthetic peptide) in Bis Tris Propane buffer with protein (bovine) stabilizer. Preservatives…
    Category
    Medical Device
    Distribution
    Distributed nationwide