The Recall Desk

State

US Virgin Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30901–30925 of 73900

  • HighNHTSA·19V876000·2019-12-11

    Toyota Recalls 2019 Prius Vehicles Due to Electrical Short Circuit Risk

    Toyota is recalling 2019 Prius vehicles because an electrical short circuit in the combination meter could cause the speedometer, odometer, and fuel gauge to go blank, increasing crash risk.

    Product
    TOYOTA — TOYOTA PRIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0555-2020·2019-12-11

    QuVa Pharma Recalls Fentanyl Infusions Due to Glass Particulate Matter

    QuVa Pharma is recalling fentanyl 10 mcg/mL infusion bags nationwide due to the potential presence of glass particulate matter.

    Product
    fentaNYL 1000 mcg/100 mL (10 mcg/mL) in 0.9% Sodium Chloride Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1092-36
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0592-2020·2019-12-11

    Stryker Recalls Disposable Tourniquet Cuffs Due to Air Leak Risk

    Stryker is recalling 16,380 disposable tourniquet cuffs because they may leak air, causing a loss of vascular occlusion during surgery.

    Product
    Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 1PRT(Single Port) Quick Connect Connector, Product Number 5921-018-135 - Product Usage: The Stryker Disposable Tourniquet Cuff (cuff) is indicated for use in surgical procedures that require the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0608-2020·2019-12-11

    Philips HeartStart XL+ Defibrillator Recall for Power-On Failure

    Philips is recalling 24,738 HeartStart XL+ Defibrillator/Monitor units because they may fail to turn on or restart, rendering them unable to return to a ready-for-use state.

    Product
    HeartStart XL+ Defibrillator/Monitor, Model 861290
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V875000·2019-12-11

    Porsche Recalls 15,501 Vehicles for Child Seat Manual Deficiency

    Porsche is recalling 15,501 vehicles because the owner's manual lacks specific instructions for installing child restraint systems, which may increase injury risk in a crash.

    Product
    PORSCHE — PORSCHE CAYMAN, 911 GT3, 911 GT3 RS, 911 R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0566-2020·2019-12-11

    QuVa Pharma Recalls Fentanyl Syringes Due to Glass Particulate Matter

    QuVa Pharma is recalling specific lots of fentanyl syringes because they may contain glass particulate matter.

    Product
    fentaNYL 1000 mcg/20 mL (50 mcg/mL) 20 mL in 20 mL Syringe Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1415-47
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0621-2020·2019-12-11

    Pacira Recalls Sub-Potent Exparel Bupivacaine Injectable Vials

    Pacira Pharmaceuticals is recalling 910 vials of Exparel (Bupivacaine) because the drug was found to be sub-potent and out of specification.

    Product
    EXPAREL — EXPAREL (BUPIVACAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0591-2020·2019-12-11

    Brasseler Twist Drills Recalled Due to Incorrect Laser Etching

    Brasseler USA is recalling 387 units of 3.5 mm twist drills that were incorrectly laser etched as 2.5 mm.

    Product
    BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm, Total Length 112mm, Effective Length, 86mm - Product Usage: Twist drill intended use: to drill into bone in hip or knee surgeries.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0603-2020·2019-12-11

    Miami Device Solutions Recalls Right Proximal Humerus Plates Due to Identification Error

    Miami Device Solutions is recalling 15 units of Right Proximal Humerus Plates because they may be improperly identified as left.

    Product
    Proximal Humerus Plate, 8 holes, Right, REF MDS130108R - Product Usage: The Proximal Humerus Plating System consists of plates, screws, and locking caps intended to provide internal fixation of fractures of the proximal humerus. The polyaxial screws have a range of motion of +…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0606-2020·2019-12-11

    Theralase TLC-2000 Laser System Recalled for Missing UDI Labels

    Theralase Inc. is recalling 41 TLC-2000 Therapeutic Medical Laser Systems because they were shipped without required Unique Device Identification (UDI) labels.

    Product
    TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0607-2020·2019-12-11

    Theralase Laser Power Pack Recalled for Missing UDI and False CE Mark

    Theralase Inc. is recalling 306 TLC-2002 Power Packs for the TLC-2000 Therapeutic Medical Laser System because they were shipped without a Unique Device Identification (UDI) label and incorrectly labeled as CE Marked.

    Product
    TLC-2000 Therapeutic Medical Laser System, Power Pack component TLC-2002 Used for the temporary relief of knee pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·119-2019·2019-12-10

    Ruiz Recalls Frozen Breakfast Burritos Due to Plastic Contamination

    Ruiz Food Products is recalling approximately 55,013 pounds of frozen breakfast burritos that may contain pieces of plastic. No injuries have been reported.

    Product
    Ruiz Food Products, Inc. — Ruiz Food Products, Inc. Recalls Frozen Sausage Breakfast Burrito Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·20038·2019-12-10

    Bass Pro Recalls MR. STEAK Gas Grills Due to Fire Hazard

    Bass Pro is recalling MR. STEAK four and five burner gas grills because the fuel line can melt and cause a fire.

    Product
    MR. STEAK four and five burner gas patio grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V874000·2019-12-10

    Spartan Emergency Response Vehicles Recalled for Brake Valve Defect

    Marion Body Works is recalling 2018-2019 Spartan Gladiator and Metro Star emergency response chassis because a brake relay valve defect may cause extended stopping distances.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V873000·2019-12-10

    Jayco Recalls 2019-2020 White Hawk Travel Trailers Due to Blocked Escape Window

    Jayco is recalling 2019-2020 White Hawk travel trailers because the rear emergency escape window cannot fully open due to a ladder. Owners should contact dealers for a free repair.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V870000·2019-12-09

    ARBOC Specialty Vehicles Recalls Spirit Models for Roof Hatch Handle Defect

    ARBOC Specialty Vehicles is recalling 2017-2019 Spirit of Freedom and Spirit of Mobility vehicles because the roof hatch handle may break, preventing emergency egress.

    Product
    ARBOC SPECIALTY VEHICLES — ARBOC SPECIALTY VEHICLES, ARBOC SPIRIT OF MOBILITY, SPIRIT OF FREEDOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20036·2019-12-06

    Surly Recalls Front Bicycle Racks Due to Crash and Injury Hazards

    Surly Bikes is recalling about 5,139 front bicycle racks because they can loosen and contact the front wheel, posing crash and injury hazards.

    Product
    Surly front bicycle racks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V866000·2019-12-06

    Volkswagen Recalls 2013-2015 Jetta Hybrid for Transmission Defect

    Volkswagen is recalling 2013-2015 Jetta Hybrid vehicles because hairline cracks in the transmission can cause oil leaks and sudden loss of drive power, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20035·2019-12-06

    Trek Recalls Super Commuter+ Electric Bicycles Due to Fall Hazard

    Trek is recalling about 2,840 Super Commuter+ 8S electric bicycles because a front fender bolt can unthread, causing the wheel to detach and posing a fall hazard.

    Product
    Trek Super Commuter+ 8S
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V869000·2019-12-06

    Daimler Recalls 2020-2021 Thomas Built Saf-T-Liner C2 School Buses

    Daimler Trucks North America is recalling 145 school buses due to loose fan hub bolts that could damage components or detach, risking injury during an uncontrolled stop.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V867000·2019-12-06

    Mercedes-Benz Recalls 2020 GLE 450 for Third-Row Headrest Defect

    Mercedes-Benz is recalling one 2020 GLE 450 4MATIC because third-row headrests may not hold in place, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide