The Recall Desk

State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39526–39550 of 73919

  • CriticalUSDA FSIS·018-2018·2018-03-02

    Olli Salumeria Americana Recalls Ready-to-Eat Meat Products Due to Listeria

    Olli Salumeria Americana is recalling approximately 3,946 pounds of ready-to-eat meat products that may be contaminated with Listeria monocytogenes.

    Product
    OLLI SALUMERIA AMERICANA — Olli Salumeria Americana Firm Recalls Ready-To-Eat Meat Products due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V143000·2018-03-02

    Keystone Recalls 2018 Recreational Trailers Due to Propane Leak Risk

    Keystone is recalling 2,958 specific 2018 recreational trailers because a loose propane valve screw may cause gas leaks and fire.

    Product
    DUTCHMEN — DUTCHMEN, KEYSTONE, CROSSROADS ASPEN TRAIL, PASSPORT, ZINGER, HIDEOUT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V144000·2018-03-02

    Newmar Recalls 2018 Essex Motorhomes Due to Taillight Detachment Risk

    Newmar is recalling 2018 Essex motorhomes because taillights may loosen and detach while driving, increasing crash risk. Dealers will secure the lights with new hardware.

    Product
    NEWMAR — NEWMAR ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18110·2018-03-01

    Double Insight Recalls Gem 65 Multicookers Due to Fire Hazard

    Double Insight is recalling Gem 65 8-in-1 multicookers sold at Walmart because a defect can cause the unit to overheat and melt, posing a fire hazard.

    Product
    Gem 65 8-in-1 multicookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V140000·2018-03-01

    Jaguar Recalls 2018 E-Pace Vehicles Due to Front Brake Hose Bracket Defect

    Jaguar is recalling 2018 E-Pace vehicles because improperly installed front brake hose brackets may allow hoses to contact tires, causing fluid leaks and increased stopping distances.

    Product
    JAGUAR — JAGUAR E-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18112·2018-03-01

    Graco Recalls Table2Table Highchairs Due to Rear Leg Fall Hazard

    Graco is recalling about 36,000 Table2Table 6-in-1 highchairs sold at Walmart because the rear legs can pivot out of position, creating a fall hazard.

    Product
    Graco Table2Table 6-in-1 Highchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V142000·2018-03-01

    Coach House Recalls RVs with Defective Kidde Fire Extinguishers

    Coach House is recalling 2003-2018 recreational vehicles equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks during a fire.

    Product
    COACH HOUSE — COACH HOUSE ARRIVA, PLATINUM II, PLATINUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V141000·2018-03-01

    Ford Recalls 2017-2018 Taurus Vehicles for Ignition Key Removal Defect

    Ford is recalling 2017-2018 Taurus vehicles because the ignition key may be removed when the transmission is not in Park, increasing the risk of the vehicle rolling away.

    Product
    FORD — FORD TAURUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V139000·2018-03-01

    Land Rover Recalls 2018 Range Rover Velar for Visibility Defect

    Jaguar Land Rover is recalling 2018 Range Rover Velar vehicles because ventilation system parts may detach, preventing fog removal from windows and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER VELAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E011000·2018-03-01

    RockyMounts Recalls Four Bicycle Rack Models Due to Weld Failure Risk

    RockyMounts is recalling four bicycle rack models because a weld may crack, causing the rack and bicycles to separate from the vehicle and create a road hazard.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0583-2018·2018-02-28

    Medtronic Recalls Compia MRI CRT-Ds Due to Therapy Prevention Risk

    Medtronic is recalling 951 Compia MRI CRT-Ds because a defect may prevent the delivery of high and low voltage therapy.

    Product
    Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Compia MRI. Labeled as the following: a. Compia MRI CRT-D DF1 (Product No. DTMC1D1); b. Compia MRI Quad CRT-D DF4 (Product No.DTMC1QQ ) Implantable devices that automatically detect and treat episodes of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0587-2018·2018-02-28

    Medtronic Recalls Evera ICDs Due to Possible Therapy Prevention

    Medtronic is recalling 951 Evera ICDs and CRT-Ds because a defect may prevent the devices from delivering high or low voltage therapy.

    Product
    Implantable Cardioverter Defibrillators (ICDs), Evera. Labeled as the following: a. Evera S DR ICD DF1 (Product No. DDBC3D1); b. Evera S VR ICD DF1 (Product No. DVBC3D1); c. Evera S VR ICD DF4 (Product No. DVBC3D4); d. Evera XT DR ICD DF1 (Product No. DDBB1D1); e.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0642-2018·2018-02-28

    Allen Medical Systems Recalls Radiolucent Surgery Spine Frames

    Allen Medical Systems is recalling 161 Radiolucent Surgery Spine Frames because the base may crack during patient transfer.

    Product
    Radiolucent Surgery Spine Frame (F70801). Surgical platform used to position patients for lumbar spine procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0453-2018·2018-02-28

    Pharmedium Recalls Ropivacaine HCl Injection Due to Sterility Assurance Concerns

    Pharmedium Services, LLC is recalling all lots of Ropivacaine HCl in 0.9% Sodium Chloride due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.

    Product
    Ropivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0443-2018·2018-02-28

    Pharmedium Recalls Adenosine Injection Due to Sterility Assurance Concerns

    Pharmedium Services, LLC is recalling all lots of Adenosine Injection because of a lack of sterility assurance. The recall covers products distributed nationwide.

    Product
    Adenosine Injection in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0465-2018·2018-02-28

    Pharmedium Recalls Meperidine HCl Injections Due To Sterility Concerns

    Pharmedium Services, LLC is recalling Meperidine HCl in 0.9% Sodium Chloride injections nationwide due to a lack of sterility assurance.

    Product
    Meperidine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0441-2018·2018-02-28

    Pharmedium Recalls Ketamine HCl Injection Due to Sterility Assurance Concerns

    Pharmedium Services, LLC is recalling all lots of Ketamine HCl in 0.9% Sodium Chloride due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.

    Product
    Ketamine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0466-2018·2018-02-28

    Pharmedium Recalls Methadone HCl Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling Methadone HCl Injection in all strengths and packaging due to a lack of sterility assurance.

    Product
    Methadone HCl Injection in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0460-2018·2018-02-28

    Pharmedium Recalls Labetalol HCl Infusions Due to Sterility Assurance Concerns

    Pharmedium Services, LLC is recalling Labetalol HCl in 0.9% Sodium Chloride infusions nationwide due to a lack of sterility assurance.

    Product
    Labetalol HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0582-2018·2018-02-28

    Medtronic Recalls Amplia MRI CRT-D Devices Due to Therapy Prevention Risk

    Medtronic is recalling 951 Amplia MRI CRT-D devices because they may fail to deliver high or low voltage therapy.

    Product
    Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Amplia MRI. Labeled as the following: a. Amplia MRI CRT-D DF4 (Product No. DTMB1D4); b. Amplia MRI Quad CRT-D DF1 (Product No. DTMB1Q1); c. Amplia MRI Quad CRT-D DF4 (Product No. DTMB1QQ); EXPANSION: d.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0588-2018·2018-02-28

    Medtronic Recalls Visia AF MRI ICDs Due to Therapy Prevention Risk

    Medtronic is recalling 951 Visia AF MRI ICDs and CRT-Ds because a defect may prevent high and low voltage therapy.

    Product
    Implantable Cardioverter Defibrillators (ICDs), Visia AF MRI. Labeled as the following: a. Visia AF MRI VR SureScan ICD DF1 (Product No. DVFB1D1); b. Visia AF MRI VR SureScan ICD DF4 (Product No. DVFB1D4); EXPANSION: c. Visia AF MRI S VR SureScan ICD DF1 (Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0437-2018·2018-02-28

    Pharmedium Recalls Morphine Sulfate in 5% Dextrose Due to Sterility Concerns

    Pharmedium Services, LLC is recalling Morphine Sulfate in 5% Dextrose in all strengths and packaging due to a lack of sterility assurance.

    Product
    Morphine Sulfate in 5% Dextrose in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0458-2018·2018-02-28

    Pharmedium Recalls Ropivacaine HCl Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling Ropivacaine HCl Injection in all strengths and packaging due to a lack of sterility assurance.

    Product
    Ropivacaine HCl Injection in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide