The Recall Desk

State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

60926–60950 of 74011

  • ModerateFDA (Devices)·Z-0337-2014·2013-11-27

    GE Healthcare Recalls Centricity Perinatal and Intensive Care Software

    GE Healthcare is recalling Centricity Perinatal and Intensive Care software due to a rare network issue that may temporarily prevent users from accessing patient rosters.

    Product
    Centricity Perinatal and Centricity Intensive Care is intended to be used in clinical departments healthcare delivery systems such as a Labor and Delivery, Postpartum Maternal Care, newborn Nursery, critical care units including Neonatal Intensive Care Units (NICU), and may also…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0311-2014·2013-11-27

    Ortho-Clinical Diagnostics Recalls VITROS dHDL Slides Due to Dispense Issues

    Ortho-Clinical Diagnostics is recalling VITROS dHDL Slides because slide dispense cartridges may cause dispensing problems.

    Product
    VITROS Chemistry Products dHDL Slides packaged as 300 slides/pack catalog number 6801895 VITROS dHDL Slides quantitatively measure HDL cholesterol (HDLC) concentration in serum and plasma using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0293-2014·2013-11-27

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Product Slides

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Product Slides due to slide dispense issues. The recall affects 544 units distributed worldwide.

    Product
    VITROS Chemistry Products AcP Slides, 90 slides/pack; catalog number 8168122 VITROS Chemistry Products AcP Slides quantitatively measure acid phosphatase (AcP) activity in serum and plasma using VITROS 950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0314-2014·2013-11-27

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Product GLU Slides

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Product GLU Slides due to slide dispense issues. The recall affects 349,072 units distributed worldwide.

    Product
    VITROS Chemistry Products GLU Slides packaged as 300 slides/pack catalog number 1707801 VITROS GLU Slides quantitatively measure glucose (GLU) concentration in serum, plasma, urine and cerebrospinal fluid using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-007-2014·2013-11-27

    Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil

    Hill Dermaceuticals is recalling specific lots of Derma-Smoothe/FS topical oil because routine testing found the active ingredient to be subpotent.

    Product
    Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil (Scalp Oil), 118.28 mL (4 Fl. oz.) bottle, Rx only, Manufactured and Distributed by: Hill Dermaceuticals, Inc., Sanford, Florida 32773, NDC 28105-149-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-008-2014·2013-11-27

    Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil

    Hill Dermaceuticals is recalling Derma-Smoothe/FS topical oil because routine testing found the active ingredient to be subpotent.

    Product
    Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil (Body Oil), 118.28 mL (4 fl. oz.) bottle, Rx only, Manufactured and Distributed by: Hill Dermaceuticals, Inc., Sanford, Florida 32773, NDC 28105-150-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·14033·2013-11-26

    Burley Recalls Tailwind Bicycle Racks for Trailercycles Due to Fall Hazard

    Burley Design is recalling Tailwind bicycle racks for trailercycles because the top portion can break, causing the trailercycle to disconnect and posing a fall hazard.

    Product
    Tailwind bicycle racks for trailercycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14031·2013-11-26

    American Boy and Girl Recalls Infant Sandals Due to Choking Hazard

    American Boy and Girl is recalling about 1,300 infant girl sandals sold at Meijer stores because the top strap can detach, posing a choking hazard to children.

    Product
    Girl's "Susan" Sandals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V584000·2013-11-25

    Ford Recalls 2013 Escape Vehicles for Fuel Line Fire Risk

    Ford is recalling 2013 Escape vehicles with 1.6L engines because a fuel line may have been installed incorrectly during a prior repair, posing a fire risk.

    Product
    FORD — FORD ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V598000·2013-11-25

    Wells Cargo Recalls Trailers Due to Door Lock Jamming Risk

    Wells Cargo is recalling 2006-2013 cargo trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside the vehicle.

    Product
    WELLS CARGO — WELLS CARGO CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V600000·2013-11-25

    Haulmark Travel Trailer Recall for Door Lock Jamming Risk

    Haulmark is recalling 2006-2013 travel trailers equipped with Fastec door locks that may jam, potentially trapping occupants inside the vehicle.

    Product
    HAULMARK — HAULMARK TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V599000·2013-11-25

    Wells Cargo Trailer Recall for Door Lock Jamming Risk

    Wells Industries is recalling 2006-2013 Wells Cargo trailers equipped with Fastec door locks because the deadbolt may jam, potentially trapping occupants inside.

    Product
    WELLS CARGO — WELLS CARGO CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V593000·2013-11-25

    Peterbilt Trucks Recalled for Missing Certification Label Information

    PACCAR is recalling 2004-2013 Peterbilt trucks because missing certification label information may lead to axle overloading or improper tire installation, increasing crash risk.

    Product
    PETERBILT — PETERBILT 385, 389, 386, 388
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V589000·2013-11-22

    Maserati Recalls 2014 Quattroporte GTS for Wiring Fire Risk

    Maserati is recalling 2014 Quattroporte GTS vehicles due to a wiring defect that could cause a fire or vehicle stall.

    Product
    MASERATI — MASERATI QUATTROPORTE GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V585000·2013-11-22

    Jayco, Starcraft, and Entegra Towable Trailer Door Lock Recall

    Jayco is recalling 2006-2014 towable trailers equipped with Fastec door locks because the key can jam the deadbolt, potentially trapping occupants inside.

    Product
    JAYCO — JAYCO, STARCRAFT, ENTEGRA TOWABLE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V591000·2013-11-22

    Volvo Bus 9700 Recalled for Insufficient Emergency Exit Windows

    Volvo is recalling 10 wheelchair-accessible 2009-2010 9700 motor coaches that lack required emergency exit windows, posing an injury risk during emergencies.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V569000·2013-11-22

    Volkswagen Recalls 2009-2011 Tiguan Vehicles for Melted Fuse Holder

    Volkswagen is recalling 2009-2011 Tiguan vehicles because a fuse holder may melt, causing partial loss of exterior lights and increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·14028·2013-11-21

    Angelcare Baby Monitors Recalled for Infant Strangulation Hazard

    Angelcare is recalling about 600,000 baby monitors in the U.S. and 182,173 in Canada due to a strangulation risk from the sensor pad cord. Two infant deaths have been reported.

    Product
    Angelcare Movement and Sound Baby Monitors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14027·2013-11-21

    ElliptiGO Recalls Outdoor Elliptical Cycles Due to Fall Hazard

    ElliptiGO is recalling about 7,200 outdoor elliptical cycles in the U.S. and Canada because the front fork or drive arm axles can detach, posing a fall hazard.

    Product
    ElliptiGO outdoor elliptical cycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide