The Recall Desk

State

US Virgin Islands product recalls

73,096 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 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10801–10825 of 73273

  • SevereCPSC·24273·2024-06-20

    Frontgate Newport Chaise Lounge Chairs Recalled for Finger Crushing and Amputation

    Cinmar recalls approximately 70,000 Frontgate Resort Collection Newport aluminum and teak chaise lounge chairs because the adjustable backrest can descend with force while seated, causing finger crushing and amputation injuries.

    Product
    Frontgate Resort Collection Newport Aluminum and Teak Chaises
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24271·2024-06-20

    myCharge POWER HUB Portable Chargers Recalled for Fire and Burn Hazards

    myCharge is recalling about 567,000 POWER HUB All-In-One 10,000mAh portable chargers sold exclusively at Costco from January 2022 through November 2023 because they can overheat while charging, posing fire and burn hazards. Two residential fires and property damage totaling approximately $165,000 have been reported.

    Product
    myCharge POWER HUB All-In-One 10,000mAh portable chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24272·2024-06-20

    JoyJolt Declan Glass Coffee Mugs Recalled for Burn and Laceration Hazards

    MM Products is recalling about 580,000 JoyJolt Declan single-wall glass coffee mugs because they can break and crack when filled with hot liquids, posing burn and laceration hazards. The mugs were sold online from September 2019 through May 2022.

    Product
    JoyJolt Drinkware Declan Single-Wall Glass Coffee Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24276·2024-06-20

    Vitamix Blending Containers and Blade Bases Recalled for Laceration Hazard

    Vitamix Ascent and Venturist Series 8-ounce and 20-ounce blending containers and blade bases can separate from their bases, exposing sharp blades. The company has received 27 reports of lacerations, including 11 from a previous 2018 recall.

    Product
    Vitamix Ascent® Series and Venturist® Series 8-ounce and 20-ounce Blending Containers and Blade Bases
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V464000·2024-06-20

    Volkswagen Atlas occupant detection wiring may deactivate the passenger airbag

    Volkswagen is recalling certain 2020-2024 Atlas and Atlas Cross Sport vehicles because a wiring fault in the passenger occupant detection system may deactivate the front passenger airbag.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24278·2024-06-20

    Orly Lavender Scented Candles Recalled for Fire and Burn Hazards

    CBOCS Distribution Inc. is recalling about 3,600 lavender scented candles in wooden bread bowls sold at Cracker Barrel Old Country Store from November 2023 through May 2024. The candle flames can reach excessive heights and ignite the wooden bowl, posing fire and burn risks.

    Product
    Lavender scented candles in a round wooden bread bowl
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24270·2024-06-20

    Yeti Link Expansion Modules and EC8 Cables Recalled for Fire and Burn Hazards

    Goal Zero is recalling about 34,460 Yeti Link Expansion Modules and EC8 Cables because the connections can overheat and melt, posing fire and burn hazards. Two reports of cables melting inside vehicles have been received with minor property damage but no injuries.

    Product
    Yeti Link Expansion Modules and EC8 Cables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24279·2024-06-20

    Cedona Natural View Six-Drawer Dressers Recalled for Tip-Over Hazard

    Global Homes USA is recalling about 400 Cedona Natural View six-drawer dressers sold at Rooms To Go for tip-over and entrapment hazards that can injure or kill children if not anchored to a wall.

    Product
    Cedona Natural View six-drawer dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24275·2024-06-20

    Babboe Cargo Bicycles Recalled for Frame Cracking and Fall Hazard

    Babboe cargo bicycles manufactured by Babboe B.V. are being recalled because their frames can crack, bend, and break, posing a fall hazard to riders. The recall affects about 300 units sold in the United States through bicycle retailers nationwide between January 2011 and March 2024.

    Product
    Cargo bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24269·2024-06-20

    StyleCraft Instinct Cordless Hair Clippers Recalled for Fire and Burn Hazards

    StyleCraft is recalling about 50,000 Instinct Professional Vector Motor Cordless Hair Clippers because the lithium-ion battery can overheat, posing fire and burn hazards. Six incidents of battery overheating or fire have been reported, including one minor burn.

    Product
    Instinct Professional Vector Motor Cordless Hair Clippers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24277·2024-06-20

    Head Rush Technologies Recalls TRUBLUE iQ Auto Belay Devices for Fall Hazard

    Head Rush Technologies is recalling TRUBLUE iQ Auto Belay Devices because they can fail to retract, creating a risk of serious injury or death from falls. About 2,200 units were sold online from November 2022 through February 2024.

    Product
    TRUBLUE iQ Auto Belay Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V461000·2024-06-20

    Toyota Grand Highlander curtain airbags may deploy outside an open window

    Toyota is recalling certain 2024 Grand Highlander and Lexus TX vehicles because the side curtain airbags may not unroll as intended and could partially deploy outside an open window.

    Product
    TOYOTA — TOYOTA, LEXUS GRAND HIGHLANDER, TX, GRAND HIGHLANDER HYBRID, TX HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24274·2024-06-20

    Theefun Kids Gardening Tools Sets Recalled for Excess Phthalates

    Theefun Kids Gardening Tools Sets (model HJL-001) are recalled because the brown handle strings contain phthalates that exceed federal safety limits. Phthalates are toxic if ingested by young children.

    Product
    Theefun Kids Gardening Tools Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V466000·2024-06-20

    Fisker Ocean exterior door handles can stick and fail to open

    Fisker is recalling all 2023-2024 Ocean vehicles because the exterior door handles can stick and fail to open, which can prevent occupants from exiting in an emergency.

    Product
    FISKER — FISKER OCEAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V459000·2024-06-20

    Cadillac XT5 and XT6 instrument panels may not illuminate signal reminders

    GM is recalling certain 2023-2025 Cadillac XT5 and XT6 vehicles because the instrument panel may not illuminate when hazard warning lights, high beams or turn signals are activated.

    Product
    CADILLAC — CADILLAC XT5, XT6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·24V458000·2024-06-20

    Rivian R1S and R1T tire placards show incorrect maximum capacity weight

    Rivian is recalling certain 2022-2023 R1S and R1T vehicles because the maximum vehicle capacity weight value on the tire placard label is incorrect, failing FMVSS 110.

    Product
    RIVIAN — RIVIAN R1T, R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0554-2024·2024-06-19

    Docetaxel Injection Recalled Nationwide for Stopper Particulate Matter

    Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper contaminating the drug. The recall affects 2,806 vials distributed nationwide.

    Product
    DOCETAXEL — DOCETAXEL (DOCETAXEL ANHYDROUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1345-2024·2024-06-19

    Baraka Brand Ground Black Pepper Recalled for Potential Salmonella Contamination

    U.B.C. Food Distributors is recalling Baraka brand ground black pepper due to potential Salmonella contamination. The product is packaged in 7oz retail containers with UPC 8 22514 26626 6.

    Product
    Baraka brand ground black pepper packaged in 7oz retail containers with UPC 8 22514 26626 6; 10 units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1347-2024·2024-06-19

    Mt. Capra Goat Milk Formula Kit Recalled for Lack of FDA Premarket Notification

    Mt. Capra Goat Milk Formula Recipe Kit recalled for marketing as infant formula without FDA premarket notification.

    Product
    Mt. Capra Goat Milk Formula Recipe Kit (net wt. 10lbs. 8oz.) and Bundle Refill. Each Goat Milk Formula Recipe Kit consist of 10 individually packaged ingredients: *Whole Goat Milk *Goat Milk Lactose *Goat Milk Ghee -Extra Virgin Olive Oil -Expeller-Pressed Grapeseed Oil
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1921-2024·2024-06-19

    Thoratec HeartMate System Monitor display malfunction in left ventricular assist devices

    The Thoratec HeartMate System Monitor is being recalled due to display malfunctions affecting 4,842 devices worldwide. These issues may prevent proper monitoring and device control.

    Product
    Thoratec HeartMate System Monitor, REF: 1286, L1286, 1286A, L1286A, 1286A-US, L1286A-US, 1286C, L1286C, L1386, 1286A-CAN, 1286INT and L1286INT. Left ventricular assist device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0553-2024·2024-06-19

    Docetaxel Injection Recalled Due to Particulate Matter in Stopper

    Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper. Lot F1040001 was distributed nationwide.

    Product
    DOCETAXEL — DOCETAXEL (DOCETAXEL ANHYDROUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2131-2024·2024-06-19

    Stimuplex A Injection Needles Recalled for DEHP Mislabeling

    B Braun Medical Inc is recalling Stimuplex A injection needles because the devices are labeled as DEHP-free, but the glue used contains traces of DEHP. The recall affects 20,850 units distributed in the US and Canada.

    Product
    Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2134-2024·2024-06-19

    Stimuplex A Nerve Needles Recalled for Mislabeled DEHP Content

    B Braun Medical Inc is recalling over 1.1 million Stimuplex A nerve block needles labeled as DEHP-free, but the adhesive contains traces of DEHP. The mislabeling poses a risk to users who selected the product specifically to avoid DEHP exposure.

    Product
    Stimuplex A, 30 DEG, 22GX2", 0.70x50mm, Catalogue Number: 4894502
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2137-2024·2024-06-19

    CODMAN EVD BACTISEAL Catheter Sterile Packaging Defect Recall

    Integra LifeSciences recalls CODMAN EVD BACTISEAL catheters due to defects in sterile packaging that may compromise product sterility. The defect affects 106 units distributed worldwide.

    Product
    CODMAN EVD BACTISEAL 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0546-2024·2024-06-19

    Zilretta Injectable Drug Recalled for Failed Stability Specifications

    Pacira Pharmaceuticals is recalling 43,768 kits of Zilretta injectable suspension due to failed stability specifications at 2–8°C storage for 12 months followed by 25°C for 6 weeks. No illnesses or injuries have been reported.

    Product
    ZILRETTA — ZILRETTA (TRIAMCINOLONE ACETONIDE EXTENDED-RELEASE INJECTABLE SUSPENSION)
    Category
    Drug
    Distribution
    Distributed nationwide