The Recall Desk

State

US Virgin Islands product recalls

73,104 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
30
Most recent
2026-09-23

Of the 177 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 30 (17%) are Severe.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11701–11725 of 73281

  • HighNHTSA·24T004000·2024-04-23

    Rocky Mountain ATV/MC Recalls Tusk 2Track Adventure Motorcycle Tires

    Rocky Mountain ATV/MC is recalling Tusk 2Track Adventure rear motorcycle tires because the tread layer was improperly cured, which can cause tread detachment and loss of vehicle control.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-04202024-001·2024-04-20

    Ground Beef Products Subject to Public Health Alert for E. Coli O157:H7

    USDA FSIS issued a public health alert for Greater Omaha Packing Co. ground beef products due to possible E. coli O157:H7 contamination. Consumers should not consume these products.

    Product
    Greater Omaha Packing Co., Inc. — FSIS Issues Public Health Alert for Ground Beef Products Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V281000·2024-04-19

    REV Ambulance Recalls 76 Vehicles Due to Electrical Fire Risk

    REV Ambulance Group Orlando is recalling 76 ambulances from 2019-2024 because a firmware defect may cause electrical circuits to overheat and increase the risk of fire.

    Product
    REV AMBULANCE — REV AMBULANCE TYPE IX, TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V284000·2024-04-19

    2024 Tesla Model 3 Side Air Bag Module Missing Deflector

    Tesla is recalling one 2024 Model 3 vehicle. The driver seat side air bag module was assembled without a deflector, which may cause improper deployment and increase the risk of injury during a crash.

    Product
    TESLA — TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V283000·2024-04-19

    2024 Hyundai IONIQ 6 Differential Gear Drive Unit Recall

    Hyundai is recalling certain 2024 IONIQ 6 vehicles because differential gear bolts in the gear drive unit may not be tightened properly, risking loss of drive power or differential lockup that could increase crash risk.

    Product
    HYUNDAI — HYUNDAI IONIQ 6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V279000·2024-04-19

    REV Recalls Fleetwood and Holiday Rambler Motorhomes for Fire Risk

    REV is recalling 2022-2024 Fleetwood Discovery and Holiday Rambler Endeavor motorhomes because inadequate fuse protection on the water pump harness may cause a fire.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER DISCOVERY, ENDEAVOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V282000·2024-04-19

    Genesis G90 fuel pump failure may cause loss of drive power

    Hyundai is recalling certain 2022–2023 Genesis GV70, GV80, G80, and G90 vehicles because the fuel pump may fail, resulting in loss of drive power and increased crash risk.

    Product
    GENESIS — GENESIS G80, GV80, GV70, G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V280000·2024-04-19

    2024 Coachmen Catalina and Forest River Aurora Travel Trailers Cooktop

    Forest River is recalling certain 2024 Coachmen Catalina and Forest River Aurora travel trailers because the cooktop-furnace isolation panel was not properly sealed during manufacturing, which could result in an inverted cooktop flame and fire risk.

    Product
    COACHMEN — COACHMEN, FOREST RIVER CATALINA, AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24201·2024-04-18

    Gasaciods Children's Multi-Purpose Helmets Recalled for Head Injury Risk

    Gasaciods children's helmets sold on Temu.com fail to meet federal safety standards for bicycle helmets and do not adequately protect against head injury in a crash. Consumers should stop using them immediately.

    Product
    Gasaciods Children's Multi-Purpose Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V278000·2024-04-18

    2022 Jaguar E-Pace passenger air bag may tear during deployment

    Jaguar is recalling certain 2021–2023 E-Pace vehicles because the passenger air bag may tear during deployment, reducing occupant protection and risking burn injury from hot gases.

    Product
    JAGUAR — JAGUAR E-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24203·2024-04-18

    Gossamer Pro AGX+ Bicycle Cranksets Recalled for Fall Injury Risk

    Full Speed Ahead is recalling Gossamer Pro AGX+ cranksets that can loosen or detach from bicycles, creating a fall hazard. The company has received 277 reports of loosening or detachment but no injuries to date.

    Product
    Gossamer Pro AGX+ cranksets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V277000·2024-04-18

    Setra S407 and S417 Wheelchair Lift Beacon Recall

    Daimler Coaches is recalling 2011-2016 Setra coaches because wheelchair lift warning beacons may be too dim, increasing injury risk.

    Product
    SETRA — SETRA S407 CC, S417 TC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24202·2024-04-18

    Randder Liquid Fuel Bottles Recalled for Non-Child-Resistant Closure

    Randder 2-Pack Liquid Fuel Bottles in 750mL and 1500mL sizes sold on Amazon are recalled because their closures do not meet child-resistant requirements under the Children's Gasoline Burn Prevention Act, posing a risk of burns and poisoning to children.

    Product
    Randder 2-Pack Liquid Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1147-2024·2024-04-17

    Dietary supplement recalled for toxic yellow oleander substitution

    Alipotec Raiz de Tejocote dietary supplements are being recalled because they contain toxic yellow oleander instead of tejocote. All 280 bottles were distributed nationwide.

    Product
    Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0440-2024·2024-04-17

    FDA Class I Recall: Methocarbamol Injection for Particulate Matter

    Eugia US LLC is recalling Methocarbamol Injection nationwide due to particulate matter contamination. The FDA classified this as a Class I recall affecting lot 3MC23011 (expiration 11/30/2026).

    Product
    METHOCARBAMOL — METHOCARBAMOL (METHOCARBAMOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V273000·2024-04-17

    Spencer Recalls 2024 Pumper Vehicles Due to Electrical Fire Risk

    Spencer is recalling 2024 Pumper vehicles because a firmware defect in specific electrical nodes may cause overloaded circuits and increase the risk of fire.

    Product
    SPENCER — SPENCER PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V276000·2024-04-17

    2024 Tesla Cybertruck Accelerator Pedal Dislodgement Recall

    Tesla is recalling certain 2024 Cybertruck vehicles because the accelerator pedal pad may dislodge and become trapped by the interior trim, potentially causing unintended acceleration and crash risk.

    Product
    TESLA — TESLA CYBERTRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1486-2024·2024-04-17

    Patient lift hanger bar may come loose, posing fall risks

    Certain patient lift models may have a hanger bar that could come loose during use, potentially causing patient falls. Approximately 10 units distributed to TX, IL, OK, and CA are affected.

    Product
    Altair 330 lbs w/o Hanger Bar, REF: 55200H-NA, 55220H-NA, and Roomer S 220 kg w/o Hanger Bar, REF: 55300H-NA, patient lifts
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1483-2024·2024-04-17

    KWIK-STIK Quality Control Kit Recalled for Fungal Contamination

    Microbiologics Inc recalls KWIK-STIK quality control kits contaminated with Aspergillus brasiliensis fungus. Users may observe unexpected fungal growth when using affected control material.

    Product
    KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b, a) REF 0209P and b) REF 0209K, Quality control kit for culture media
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1487-2024·2024-04-17

    Medline Adult Portable Bed Rails Recalled for Safety Standard Failures

    Medline is recalling certain lots of adult portable bed rails that were manufactured after the mandatory compliance date but failed to meet required safety standards, potentially posing a fall risk.

    Product
    Bed Assist Bars, labeled as follows: a) Medline, Model Number BA6800, b) Medline Martha Stewart, Model Number MDS6800BAMMS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1507-2024·2024-04-17

    CT Scanner Software Upgrade May Cause Unexpected Table Movement

    Philips CT scanner software upgrade may cause the patient tabletop to move unexpectedly during scan initialization, posing collision risk to nearby operators or bystanders.

    Product
    PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to V4.5.1.41989-Intended to produce cross-sectional images of the body Model Number: 728143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1495-2024·2024-04-17

    ConvaTec CarboFlex Wound Dressing Recalled for Failed Sterility Standards

    ConvaTec is recalling 63 market units of CarboFlex odor control dressings that fail to meet sterility assurance requirements. Affected lots were distributed in six states.

    Product
    ConvaTec CarboFlex, 15cm x 20cm, 6 in. x 8 in., Order No. 403204, Odor Control Dressing, Sterile. Packaged 1 dressing/immediate package, 5 packages/market unit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1496-2024·2024-04-17

    Acetabular Fixation Cups Recalled for Marketing Without FDA Clearance

    Synovo Production is recalling 764 acetabular fixation cups marketed without FDA clearance or approval. These hip replacement components were distributed nationwide in Washington state.

    Product
    ACETABULAR FIXATION CUP, (xx)MM, 5 HOLE, Ti-6AI-4V ELI TiN CERAMIC W/PLASMA SPRAY, STERILEEO, Reference Numbers: 01-01-0554 01-01-0556 01-01-0558 01-01-0560 01-01-0562 01-01-0564 01-01-0566
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1515-2024·2024-04-17

    Feeding tube kit recalled due to blocked connector preventing guidewire advancement

    Boston Scientific's EndoVive 20Fr PEG kit may have a blocked connector preventing proper guidewire advancement during placement, potentially requiring emergency intervention.

    Product
    EndoVive 20Fr Push Safety PEG Kit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00566471
    Category
    Medical Device
    Distribution
    Distributed nationwide