The Recall Desk

State

US Virgin Islands product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28351–28375 of 73762

  • SevereNHTSA·20V400000·2020-07-10

    Forest River Recalls 2021 Riverstone Trailers Due to Wiring Defect

    Forest River is recalling specific 2021 Riverstone trailers equipped with an optional generator prep package due to incorrect transfer switch wiring that may cause voltage back feed.

    Product
    FOREST RIVER — FOREST RIVER RIVERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20761·2020-07-09

    RH Recalls Riveted Mesh Floor Lamps Due to Fire Hazard

    RH is recalling Riveted Mesh Floor Lamps because the foot switch can overheat or catch fire. Consumers should stop using the lamps and contact RH for a refund.

    Product
    Riveted Mesh Floor Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20759·2020-07-09

    Ananda Apothecary Recalls Essential Oils Due to Non-Child-Resistant Packaging

    Ananda Apothecary is recalling four essential oil products because their packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.

    Product
    Wintergreen 100% Pure Essential Oil, Sweet Birch 100% Pure Essential Oil, Super Soother Pure Essential Oil Blend, and Breathe Deep Pure Essential Oil Blend
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1027-2020·2020-07-08

    Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert Recalled for Undeclared Milk

    Beyond Better Foods is recalling Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert because it may contain undeclared milk.

    Product
    Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert, one Pint (473 ml). Case GTIN: 1-08-52109-33106-9. Item UPC:8-52109-33150-5. Produced exclusively for: Beyond Better Foods, LLC, Bronx, NY
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1015-2020·2020-07-08

    Mount Franklin Foods Recalls 7-Select Yogurt Pretzels for Undeclared Peanuts

    Mount Franklin Foods is recalling 7-Select Yogurt Pretzels because they may contain undeclared peanuts. The product was distributed to 7-11 stores nationwide.

    Product
    7-Select Yogurt Pretzels Naturally Flavored Vanilla Crunchy Pretzel Covered in a Vanilla Yogurt NET WT 5 OZ (142 g) UPC 5254856657
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1359-2020·2020-07-08

    Koala Hand Sanitizer Recalled for Subpotent Ethanol and Undeclared Isopropyl Alcohol

    Beaming White LLC is recalling Koala Hand Sanitizer because the ethanol content is below the label claim and undeclared isopropyl alcohol is present.

    Product
    Koala Hand Sanitizer, Unscented, 16 FL OZ., Antibacterial, (Ethyl Alcohol 70%), Manufactured by Beaming White LLC, 1205 NE 95th St., Vancouver, WA 98665
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1357-2020·2020-07-08

    Koala Hand Sanitizer Recalled for Subpotent Alcohol and Undeclared Ingredients

    Beaming White LLC is recalling Koala Hand Sanitizer because the ethanol level is below the label claim and it contains undeclared isopropyl alcohol.

    Product
    Koala Hand Sanitizer, Soothing Eucalyptus, 16 FL OZ., Antibacterial, (Ethyl Alcohol 68%), Manufactured by Beaming White LLC, 1205 NE 95th St., Vancouver, WA 98665
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1360-2020·2020-07-08

    Metformin Hydrochloride Extended-Release Tablets Recalled for NDMA Impurity

    The Harvard Drug Group is recalling Metformin Hydrochloride Extended-Release Tablets due to potential NDMA impurity levels above established limits.

    Product
    Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, 100 Tablets (10 x 10) unit dose cartons, Rx only, Manufactured by: Apotex, Inc., Toronto, Ontario, Canada, Manufactured for: Apotex Corp. Weston, FL, Distributed by: Major Pharmaceuticals, Livonia, MI 48152 NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1358-2020·2020-07-08

    Koala Hand Sanitizer Recalled for Subpotent Ethanol and Undeclared Isopropyl Alcohol

    Beaming White LLC is recalling Koala Hand Sanitizer because the active ingredient ethanol was tested below the label claim and undeclared isopropyl alcohol was present.

    Product
    Koala Hand Sanitizer, Menthol, 16 FL OZ., Antibacterial, (Ethyl Alcohol 69%), Manufactured by Beaming White LLC, 1205 NE 95th St., Vancouver, WA 98665
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1019-2020·2020-07-08

    Trident Seafoods Recalls Imitation Crab Supreme Due to Undeclared Egg

    Trident Seafoods is recalling Gordon Choice Imitation Crab Supreme Style because the product may contain undeclared egg white.

    Product
    Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution exclusively by Gordon Food Service Wyoming, MI 49509
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V399000·2020-07-08

    Kia Recalls 2020 Sedona Vehicles Due to Alternator Fire Risk

    Kia is recalling 2020 Sedona vehicles because a loose alternator terminal nut may cause electrical arcing and increase the risk of a fire.

    Product
    KIA — KIA SEDONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1014-2020·2020-07-08

    Brill Frozen Cookie Dough Recalled for Undeclared Walnuts

    Brill Inc. is recalling 252 cases of frozen cookie dough because the product may contain undeclared walnuts, a major food allergen.

    Product
    Brill 30 lb. cases of 480 1.0 oz. chocolate chip with mini colored candy pieces frozen cookie dough, MDM # 10194626, Manufactured by Brill, Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2437-2020·2020-07-08

    Siemens CentraLink Software Recalled for Potential Erroneous Patient Results

    Siemens Healthcare Diagnostics is recalling CentraLink Data Management System software versions 16.0.2 and 16.0.3 due to a defect that may cause erroneous patient results.

    Product
    (1) CentraLink Data Management System software version 16.0.2 Siemens Material Number (SMN): 11313246 (2) CentraLink Data Management System software version 16.0.3 Siemens Material Number (SMN): 11314337 Product Usage: are clinical laboratory information modules which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2479-2020·2020-07-08

    Preventice BodyGuardian Heart Remote Monitoring Kit Recalled for Data Accuracy Issues

    Preventice Services is recalling eight BodyGuardian Heart Remote Monitoring Kits because unvalidated software may cause inaccurate data collection, making patient reports unreliable for condition evaluation.

    Product
    BodyGuardian Heart Remote Monitoring Kit, consisting of two BG Heart monitors, either Models BC-1001-A or BC1001-D, and a cell phone, either Models BP1008 or BP10014, that is paired to both of the monitors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20E047000·2020-07-08

    TAP Recalls Rubicon Express Suspension Lift Kits for Jeep Gladiator

    TAP Worldwide is recalling certain Rubicon Express suspension lift kits for 2020-2021 Jeep Gladiators because the fitment guide inaccurately lists 40-inch tires as compatible, which can affect vehicle stability.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2468-2020·2020-07-08

    Radiometer ABL80-FLEX CO-OX Box Label Recall for Barcode Misinterpretation

    Radiometer Medical ApS is recalling ABL80-FLEX CO-OX box labels because barcode misinterpretation on analyzers may cause patient mix-ups or delayed treatment.

    Product
    ABL80-FLEX CO-OX 393-841 Box Label, REF 393-841, IVD, CE, UDI: 05700693938417 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care setting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2470-2020·2020-07-08

    Siemens IMMULITE 2000 XPi Analyzer Recalled for Tubing Crack Risk

    Siemens Healthcare Diagnostics Inc. is recalling 2,925 IMMULITE 2000 XPi Immunoassay Systems because flexible tubing can crack, causing liquid waste leaks and slip hazards.

    Product
    Siemens IMMULITE 2000 XPi Immunoassay System - In vitro Chemistry Analyzer SMN #10373214 - Product Usage: are intended for professional use in a laboratory environment only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2469-2020·2020-07-08

    Siemens IMMULITE 2000 Analyzer Recalled for Tubing Crack Hazard

    Siemens Healthcare Diagnostics is recalling 1,555 IMMULITE 2000 analyzers because flexible tubing can crack, causing liquid waste leaks and slip hazards.

    Product
    Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer SMN #10380062 - Product Usage: are intended for professional use in a laboratory environment only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20145·2020-07-08

    GloryBee Wintergreen Essential Oil Recalled for Packaging Defect

    GloryBee Natural Sweeteners is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    GloryBee Wintergreen Essential Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2438-2020·2020-07-08

    Siemens Atellica Data Manager Software Recalled for Potential Erroneous Patient Results

    Siemens Healthcare Diagnostics is recalling Atellica Data Manager software versions 1.0 and 1.1 because unexpected interface driver behavior may cause quality control results to be assigned to incorrect control lot numbers, potentially leading to the reporting of erroneous patient results.

    Product
    (1) Atellica Data Manager software version 1.0 Siemens Material Number (SMN): 11314237 (2) Atellica Data Manager software version 1.1 Siemens Material Number (SMN): 11316888 Product Usage: are clinical laboratory information modules which consolidate test orders and test…
    Category
    Medical Device
    Distribution
    Distributed nationwide