The Recall Desk

State

US Virgin Islands product recalls

73,597 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 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29576–29600 of 73775

  • ModerateCPSC·20094·2020-03-18

    Belle Chemical Recalls Drain Cleaner for Missing Poison Labeling

    Belle Chemical is recalling 100% Sodium Hydroxide Drain Cleaner because the label violates the Federal Hazardous Substance Act by omitting the word 'poison' and mandatory hazard statements.

    Product
    100% Sodium Hydroxide Drain Cleaner
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0998-2020·2020-03-18

    Mayne Pharma Recalls Carbidopa and Levodopa Tablets Due to Foreign Tablet Mix-Up

    Mayne Pharma is recalling specific bottles of Carbidopa and Levodopa Tablets because a foreign tablet was found in a bottle.

    Product
    Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-858-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1459-2020·2020-03-18

    Braemar DL900 Holter Monitor Recalled for Operational Failure

    Braemar Manufacturing is recalling DL900 Holter Monitors because a software issue prevents new patient studies from starting. Existing recordings can still be downloaded.

    Product
    Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr. Suite 150 Eagan, MN 55121 USA Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1469-2020·2020-03-18

    Binding Site Recalls VaccZyme Human Anti-Haemophilus Influenza Type B Assay Kits

    The Binding Site Group is recalling 462 VaccZyme assay kits due to performance deterioration that may cause falsely elevated antibody results.

    Product
    VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For in vitro diagnostic use, Product Code: MK016 - Product Usage: This assay is designed for the in vitro measurement of specific IgG antibodies against Haemophilus influenzae type b (Hib) capsular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1470-2020·2020-03-18

    Integra NeuraGen Nerve Guide Recalled for Quality Control Error

    Integra LifeSciences is recalling 55 units of NeuraGen Nerve Guides because nonconforming product was mistakenly released for commercial use.

    Product
    NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1055-2020·2020-03-18

    Lupin Recalls Bekyree Tablets Due to Content Uniformity Failures

    Lupin Pharmaceuticals is recalling specific lots of Bekyree oral contraceptives because they failed content and blend uniformity tests.

    Product
    Bekyree (desogestrel and ethinyl estradiol tablets USP, 0.15 mg/0.02 mg and ethinyl estradiol tablets USP, 0.01 mg), packaged in 1 Wallet of 28 Tablets (NDC 68180-879-11), 3 Wallets of 28 Tablets Each per carton (NDC 68180-879-13), Rx Only, Distributed by: Lupin Pharmaceuticals…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·20090·2020-03-17

    Honda Recalls Portable Generators Due to Fire and Burn Hazards

    American Honda is recalling about 340,000 portable generators because the inverter assembly can short-circuit in salt water, causing smoke or fire.

    Product
    Honda EB2200i, EU2200i, EU2200i Companion and EU2200i Camo Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V148000·2020-03-17

    2020 Thor Sequence motorhomes recalled for transmission shifter cable separation

    Thor Motor Coach is recalling 2020 SEQUENCE motorhomes because the transmission shifter cable may separate from the transmission, potentially causing unintended vehicle movement and increased crash risk.

    Product
    THOR — THOR, THOR MOTOR COACH SEQUENCE, TELLARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V150000·2020-03-17

    Triumph Recalls Trophy Motorcycles Due to Brake Hose Routing Defect

    Triumph is recalling 2013-2017 Trophy SE A1 motorcycles because improper brake hose routing may damage ignition wiring, causing engine stalls or lighting loss.

    Product
    TRIUMPH — TRIUMPH TROPHY, TROPHY SE A1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V149000·2020-03-16

    Audi Recalls Q7 and Q8 Models Due to Steering Shaft Bolt Issue

    Volkswagen Group of America is recalling 2017-2019 Audi Q7 and 2019 Q8 vehicles because a steering shaft bolt may loosen, potentially causing a loss of steering control.

    Product
    AUDI — AUDI Q7, Q8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V147000·2020-03-16

    Eldorado World Trans Recalled for Improperly Secured Seat Belts

    Eldorado National-Kansas is recalling 2017-2019 World Trans vehicles because seat belts may not be properly secured to the side wall, increasing injury risk in a crash.

    Product
    ELDORADO — ELDORADO WORLD TRANS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20T006000·2020-03-13

    Tornel Deportiva Tires Recalled for Tread Separation Risk

    Tornel is recalling specific Deportiva tires where adhesive failure may cause tread separation, increasing the risk of vehicle control loss and crashes.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V145000·2020-03-13

    Nissan Recalls 2020 Infiniti Q60 Vehicles for Rear Seat Belt Defect

    Nissan is recalling 2020 Infiniti Q60 vehicles because the rear seat belt locking mechanism may fail to lock properly, increasing injury risk in crashes.

    Product
    INFINITI — INFINITI Q60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V142000·2020-03-12

    GM Recalls 2020 Silverado and Sierra Trucks for Hood Latch Defect

    General Motors is recalling 2020 Chevrolet Silverado and GMC Sierra trucks because improperly heat-treated hood-latch wires may fracture, allowing the hood to open while driving.

    Product
    GMC — GMC, CHEVROLET SIERRA 3500, SILVERADO 2500, SILVERADO 3500, SIERRA 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V146000·2020-03-12

    BMW Recalls 2019-2020 Motorcycles Due to Flashing Brake Light Defect

    BMW is recalling specific 2019-2020 motorcycles because the brake light may flash instead of staying steady during emergency braking, which can confuse other drivers.

    Product
    BMW — BMW S1000 R, F 850 GS ADVENTURE, F 900 R, R NINE T SCRAMBLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20089·2020-03-12

    Yamaha Recalls Line 6 Relay G10 Wireless Guitar Systems for Fire Hazards

    Yamaha is recalling Line 6 Relay G10 wireless guitar systems because the lithium-ion battery can overheat and the cover can separate, posing fire and injury risks.

    Product
    Line 6 Relay G10 Digital Wireless Guitar Systems and USB Charging Cables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20088·2020-03-12

    Kichler Recalls 52-inch LED Ceiling Fans Due to Blade Detachment Hazard

    Kichler Lighting is recalling 52-inch LED ceiling fans because the arms holding the blades can detach, posing an injury risk. No injuries have been reported.

    Product
    Kichler 52-inch LED Indoor Ceiling fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide