The Recall Desk

State

US Virgin Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43401–43425 of 73984

  • HighFDA (Drugs)·D-0757-2017·2017-05-24

    Key Pharmacy Recalls PGE1/Procaine Injection Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of PGE1/Procaine injection because the firm cannot ensure the sterile compounded drugs are free from contamination.

    Product
    PGE1/PROCAINE 5ML MDV 40MCG/ML/0.1% INJ, Injection, 40mcg/mL, 0.1%, Rx only, 5 mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0772-2017·2017-05-24

    Key Pharmacy Recalls Procaine HCL Injections Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of Procaine HCL 1% injections because the firm cannot ensure the products are sterile.

    Product
    PROCAINE HCL *5ML* SDV SULFITE FREE 1% INJ, Injection, 1%, RXxonly, 5mL Glass/Single Dose vials, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0722-2017·2017-05-24

    Key Pharmacy Recalls Hydroxo-B12 Injections Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of Hydroxo-B12 injections because the firm cannot assure the sterility of the products.

    Product
    HYDROXO-B12 1ML SDV 10MG/ML INJ, Injection, 10mg/mL, Rx only, 1 mL glass/ Single Dose vial, Prepared by Key Compounding Pharmacy HYDROXO-B12 2ML SDV 10MG/ML INJ, Injection, 10mg/mL, RX only, 2 mL glass/ Single Dose vial.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V339000·2017-05-24

    Keystone Springdale RVs Recalled for Incorrect Weight Rating Labels

    Keystone is recalling 2012-2018 Springdale 303BH RVs because Federal Identification Tags overstate axle weight capacity, potentially leading to vehicle overload.

    Product
    KEYSTONE — KEYSTONE SPRINGDALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2110-2017·2017-05-24

    Molnlycke Recalls Brennen Skin Graft Mesher Due to Sterilization Failure

    Molnlycke Health Care is recalling 956 units of the Brennen Skin Graft Mesher because of a sterilization validation failure. The instruments were distributed domestically and internationally.

    Product
    Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2105-2017·2017-05-24

    Medline Recalls 10 mm Distraction Pins Due to Sterile Seal Concerns

    Medline Industries is recalling 10 mm Distraction Pins because the sterile packaging seal may be compromised, potentially causing the device to lose sterility.

    Product
    10 mm Distraction Pin, Aggressive Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2239-2017·2017-05-24

    Herbalife Recalls Peanut Butter Protein Bars Due to Fish Gelatin

    Herbalife is recalling Peanut Butter Protein Bars because they may contain trace amounts of fish gelatin, an undeclared allergen.

    Product
    Protein Bar 14 bars/box, Net Wt. 19.74oz (560g) Each shipping carton contains 12 boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0790-2017·2017-05-24

    Taro Recalls Fluocinonide Cream Due to Hydrocortisone Contamination

    Taro Pharmaceuticals is recalling specific lots of Fluocinonide Cream 0.05% due to cross-contamination with hydrocortisone-17-valerate.

    Product
    FLUOCINONIDE — FLUOCINONIDE (FLUOCINONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2104-2017·2017-05-24

    Medline Recalls Distraction Pins Due to Potential Sterility Loss

    Medline Industries is recalling 2,112 packs of sterile distraction pins because the packaging seal may be compromised, risking loss of sterility.

    Product
    16 mm [or 18 mm] Distraction Pin, Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2107-2017·2017-05-24

    Medline 12 mm Distraction Pin Recalled for Potential Sterility Loss

    Medline Industries is recalling 300 packs of 12 mm Distraction Pins because the sterile packaging seal may be compromised, potentially allowing the device to lose sterility.

    Product
    12 mm Distraction Pin, Blunt Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2116-2017·2017-05-24

    Medtest Holdings Recalls Pointe Scientific Hitachi AST Reagent Due to Labeling Discrepancy

    Medtest Holdings is recalling Pointe Scientific Hitachi AST Reagent because the package insert contains inconsistent linearity values in different sections.

    Product
    Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle w/PP plastic cap. R2: PE plastic bottle w /PP plastic cap. Product Usage: Two Part Chemistry Reagent For the quantitative determination of Aspartate Aminotransferase (ASl) in human serum on Hitachi analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17164·2017-05-23

    Pier 1 Imports Recalls Temani Wicker Furniture for Lead Paint Violation

    Pier 1 Imports is recalling Temani wicker chairs, settees, and ottomans because the paint may contain excessive lead, violating federal standards.

    Product
    Temani ivory wicker chair, settee and ottoman
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17166·2017-05-23

    Hobby Lobby Recalls Easter and July 4th Light-Up Spinner Toys

    Hobby Lobby is recalling Easter and July 4th-themed light-up spinner toys because the battery cover can detach, exposing coin cell batteries that pose choking and ingestion hazards to young children.

    Product
    Easter and July 4th-themed Light-Up Spinner Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V334000·2017-05-23

    REV Road Rescue Emergency Vehicles Recalled for Cot Securing Bolt Defect

    REV is recalling 24 Road Rescue emergency vehicles because short bolts may fail to secure the cot during a crash, potentially injuring occupants.

    Product
    ROAD RESCUE — ROAD RESCUE TYPE IX, TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V335000·2017-05-23

    Keystone Recalls 2017-2018 Dutchmen Voltage Trailers Due to Fuel Line Defect

    Keystone RV Company is recalling 2017-2018 Dutchmen Voltage trailers with Onan 5.5 generators because an incorrectly clamped fuel line may disconnect, causing a fuel leak and fire risk.

    Product
    DUTCHMEN — DUTCHMEN VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17162·2017-05-23

    Dynacraft Recalls Ride-On Toys Due to Sticking Pedal Hazard

    Dynacraft is recalling about 20,000 Surge and Tonka battery-operated ride-on toys because the acceleration pedal can stick, posing fall and crash hazards.

    Product
    Surge and Tonka battery operated ride-on toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17T010000·2017-05-23

    Kenda Kenetica Tires Recalled for Steel Belt Void Risk

    American Kenda Rubber Industrial is recalling specific Kenetica tires due to a void in the steel belt that may cause tread separation or sudden air loss.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V331000·2017-05-22

    Ford Recalls 2015-2017 F-Series Trucks for Door Handle Cover Defect

    Ford is recalling specific 2015-2017 F-Series trucks equipped with chrome door handle covers that may cause doors to unlatch in a side impact, increasing injury risk.

    Product
    FORD — FORD F-150, redundant F-350, redundant F-250, F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V332000·2017-05-22

    Ford Recalls 2017 Models for Manual Seat Recliner Weld Defect

    Ford is recalling 2017 Explorer and F-Series trucks because manual seat back recliners may have inadequate welds, increasing injury risk in a crash.

    Product
    FORD — FORD EXPLORER, F-150, F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V333000·2017-05-22

    Harley-Davidson Recalls 2017 Motorcycles Due to Oil Cooler Line Clamp Defect

    Harley-Davidson is recalling 45,589 2017 motorcycles because an improperly installed clamp may cause the engine oil cooler line to detach, increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHTCU, FLTRX, FLHTP, FLHRXS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·17159·2017-05-19

    Blomberg and Summit Electric Ranges Recalled for Electrocution Hazard

    Arçelik A.S. is recalling about 6,300 Blomberg and Summit electric ranges because they can become energized, posing shock and electrocution risks.

    Product
    Blomberg and Summit electric ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V330000·2017-05-19

    Columbia Aliner Ascape Trailers Recalled for Loose Propane Gas Trays

    Columbia Northwest is recalling 2017-2018 Aliner Ascape trailers because liquid propane gas bottle trays may detach, increasing the risk of fire or crash.

    Product
    COLUMBIA — COLUMBIA ALINER ASCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide