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.

58051–58075 of 74005

  • SevereNHTSA·14V383000·2014-06-27

    Special Fleet Recalls Modified Ford Super Duty Trucks Due to Fire Risk

    Special Fleet Service is recalling 2009-2013 modified Ford F-350, F-450, and F-550 trucks because oil leaks from the PTO pressure switch may ignite the exhaust thermal blanket.

    Product
    SPECIAL FLEET — SPECIAL FLEET FORD F-350, FORD F-550, FORD F-450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V378000·2014-06-27

    Jomac Recalls 2009-2013 Ford Super Duty Vehicles Due to Fire Risk

    Jomac is recalling 2009-2013 Ford F-350, F-450, and F-550 vehicles modified with specific PTO assemblies because oil leaks may cause a fire.

    Product
    JOMAC — JOMAC FORD F-550, FORD F-350, FORD F-450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V375000·2014-06-27

    GM Recalls 2013-2014 Chevrolet Caprice and SS for Wiper Defect

    General Motors is recalling 2013-2014 Chevrolet Caprice and 2014 Chevrolet SS vehicles because windshield wiper motor gears may strip, causing wipers to stop working and reducing visibility.

    Product
    CHEVROLET — CHEVROLET CAPRICE, CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V371000·2014-06-26

    Terex Recalls Aerial Devices Due to Oil Leak Fire Risk

    Terex is recalling 2009-2013 aerial devices mounted on Ford Super Duty chassis because oil may leak onto the exhaust, increasing fire risk.

    Product
    TEREX — TEREX TPL40, HR40, NT29, TL37
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V373000·2014-06-26

    Chrysler Recalls 2008-2010 Minivans and SUVs for Ignition Switch Defect

    Chrysler is recalling specific 2008-2010 Dodge and Chrysler vehicles because the ignition switch may move out of the run position, turning off the engine and disabling safety systems.

    Product
    DODGE — DODGE, CHRYSLER GRAND CARAVAN, JOURNEY, TOWN AND COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V372000·2014-06-26

    GM Recalls 2013-2014 Chevrolet Cruze for Driver Air Bag Defect

    General Motors is recalling 2013-2014 Chevrolet Cruze vehicles because the driver's air bag inflator may rupture in a crash, potentially causing serious injury.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V377000·2014-06-26

    GM Recalls 2014 Chevrolet Corvette for Rear Shock Absorber Weld Defect

    General Motors is recalling 2014 Chevrolet Corvettes because improper rear shock absorber welds may cause the tubes to separate, leading to sudden handling changes and increased crash risk.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14738·2014-06-26

    Roland Recalls RD-800 Digital Pianos Due to Electrical Shock Hazard

    Roland is recalling approximately 640 RD-800 digital pianos because the AC power cord can be connected to XLR output jacks, posing an electrical shock hazard.

    Product
    Digital Electric Piano
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V376000·2014-06-26

    Monroe Recalls Ford F-Series Trucks Due to Fire Risk

    Monroe Truck Equipment is recalling 2009-2013 Ford F-350, F-450, and F-550 trucks modified with specific PTO assemblies. Oil leaks from the PTO pressure switch may soak the exhaust thermal blanket, increasing fire risk.

    Product
    MONROE — MONROE FORD F-550, FORD F-350, FORD F-450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1392-2014·2014-06-25

    John W Hollis Inc Recalls Testosterone Cypionate Injection Due to Sterility Concerns

    John W Hollis Inc is recalling specific lots of Testosterone Cypionate for Injection because the products lack assurance of sterility.

    Product
    Testosterone Cypionate for Injection, each mL contains Testosterone Cypionate 200 mg, also contains: Cotton Seed Oil, Benzyl Benzoate, Benzyl Alcohol, Rx Only, 10 mL, JOHN HOLLIS Pharmacist, Inc. 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1395-2014·2014-06-25

    John W Hollis Recalls Levocarnitine Injection Due to Sterility Concerns

    John W Hollis Inc. is recalling Levocarnitine Solution for injection because the company cannot ensure the product is sterile. The recall covers specific lots distributed nationwide.

    Product
    Levocarnitine Solution for injection, l-Carnitine 50 mg, Also Contains Sterile Water for Injection and Benzyl Alcohol pH adjusted with HCl, 50 mL, JOHN HOLLIS Pharmacist, Inc. 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·14215·2014-06-25

    Scott and Trek Bicycles Recalled for Front Fork Crash Hazard

    Scott and Trek are recalling 2011-2013 bicycles with specific SR Suntour front forks that can break, posing a crash hazard.

    Product
    SR Suntour forks on model year 2011 through 2013 Scott and Trek bicycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1388-2014·2014-06-25

    John W Hollis Recalls Polidocanol Injection Due to Sterility Concerns

    John W Hollis Inc is recalling Polidocanol 0.5% Solution for Injection because the products lack assurance of sterility.

    Product
    Polidocanol 0.5% Solution for Injection, Polidocanol (Laureth 9) 5mg, 50 mL, JOHN HOLLIS Pharmacist Inc, 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1396-2014·2014-06-25

    John W Hollis Inc Recalls Methylcobalamin Injectable Due to Sterility Concerns

    John W Hollis Inc is recalling Methylcobalamin 1000 mcg injectable products because they lack assurance of sterility. The recall covers Lot # 1862 distributed nationwide.

    Product
    METHYLCOBALAMIN FOR INTRAMUSCULAR OR SUBCUTANEOUS USE ONLY, Methylcobalamin 1000 mcg, Also Contains: Benzyl Alcohol, Sodium Chloride, Water, Hydrochloric Acid, and/or Sodium Hydroxide, 30 mL, JOHN HOLLIS Pharmacist, Inc. 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1390-2014·2014-06-25

    John W Hollis Inc Recalls Cyanocobalamin Injection Due to Sterility Concerns

    John W Hollis Inc is recalling specific lots of Cyanocobalamin injection because the products lack assurance of sterility. The recall covers 2,650 mL distributed nationwide.

    Product
    CYANOCOBALAMIN FOR INTRAMUSCULAR OR SUBCUTANEOUS USE ONLY, Each mL contains: Cyanocobalamin 1000 mcg, , Also Contains: Benzyl Alcohol, Sodium Chloride, Water, Hydrochloric Acid, and/or Sodium Hydroxide, 30 mL, JOHN HOLLIS Pharmacist Inc, 110 20th Avenue N, Nashville, TN 37203…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1404-2014·2014-06-25

    John W Hollis Inc Recalls Lipotropic Gold Injectable Due to Sterility Concerns

    John W Hollis Inc is recalling 80 mL vials of Lipotropic Gold injectable products because they may lack sterility assurance.

    Product
    LIPOTROPIC GOLD, Each mL contains: Levocarnitine 5 mg, Thiamine 50 mg, Riboflavin-5 phosphate 5mg, Niacinimide 50mg, Calcium Pantothenate 5 mg, Cyanocobalamin 1mg, Methionine 12.5mg, Choline 25mg, Inositol 25 mg, Sterile Water For injection, JOHN HOLLIS Pharmacist, Inc,110 20th…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1398-2014·2014-06-25

    John W Hollis Inc Recalls B-Complex/Adenosine Injectable Solution for Sterility Concerns

    John W Hollis Inc is recalling B-Complex/Adenosine Injectable Solution due to a lack of sterility assurance in the compounded aseptically filled products.

    Product
    B-Complex/Adenosine Inj sol, Adenosine-5-Monophosphate 0.03g, Choline Chloride 0.01g, Cyanocobalamin 0.3mg, Inositol 0.05g, Methionine 0.015g, Levocarnitine 0.1g, Chromic Chloride 0.15g, Lidocaine HCl 0.01g, Pyrodoxine HCl 0.005g, 30 mL, JOHN HOLLIS Pharmacist, Inc, 110 20th…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1393-2014·2014-06-25

    John W Hollis Inc Recalls MIC Plus B12 Injectable Due to Sterility Concerns

    John W Hollis Inc is recalling MIC Plus B12 injectable vials because the products lack assurance of sterility. Consumers should stop using the affected lots immediately.

    Product
    MIC PLUS B12, Adenosine, L-Carnitine, Contains: Methionine 15mg, Choline 100mg, Inositol 50mg, B 12, 0.200mg, Adenosine 20mg, L-Carnitine 30mg/ML, 30ML MULTI DOSE VIAL, BENZYL ALCOHOL AS A PRESERVATIVE, JOHN HOLLIS Pharmacist, Inc, 110 20th Avenue N, Nashville, TN 37203…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1400-2014·2014-06-25

    John W Hollis Inc Recalls Compounded Injectable Drugs Due to Sterility Concerns

    John W Hollis Inc is recalling compounded Papaverine HCl and Phentolamine Mesylate injectable products due to a lack of assurance of sterility.

    Product
    Papaverine HCl 30 mg, Phentolamine Mesylate 1 mg, a) 5 mL and b) 10 mL, JOHN HOLLIS Pharmacist, Inc 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2029-2014·2014-06-25

    Anhing Recalls Caravelle Chili Powder Due to Salmonella Risk

    Anhing Corporation is recalling Caravelle Chili Powder because it may be contaminated with Salmonella. The recall covers 83 cartons distributed nationwide.

    Product
    Caravelle CHILI POWDER HOT Net Weight 8 oz. (227G), plastic tub, UPC 080736115551. 24 units/case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1402-2014·2014-06-25

    John W Hollis Inc Recalls Compounded Injectable Products Due to Sterility Concerns

    John W Hollis Inc is recalling compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of assurance of sterility.

    Product
    Papaverine HCl 30 mg, Phentolamine Mesylate 0.5 mg, Alprostadil 10 mcg, a) 5 mL and b) 10 mL, JOHN HOLLIS Pharmacist, Inc, 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide