The Recall Desk

State

US Virgin Islands product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27926–27950 of 73762

  • HighNHTSA·20V498000·2020-08-21

    Thor Motor Coach motorhomes recalled for potential electrical fire risk

    Thor Motor Coach is recalling 2019-2021 Windsport and Hurricane motorhomes due to a circuit board defect that could cause fire. The electrical control center may be damaged by voltages over 17 volts.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E057000·2020-08-20

    Motorcar Parts Recalls Duralast Brake Master Cylinders for Volkswagen Models

    Motorcar Parts of America is recalling specific Duralast brake master cylinders for Volkswagen vehicles due to a defect that may cause loss of braking.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V495000·2020-08-20

    2021 BMW Motorcycles Recalled for Detachable Tire Pressure Labels

    BMW is recalling 2021 R 1250 motorcycles (R, RT, RS, GS models) because tire pressure labels may detach from the frame. Without proper tire pressure information readily available, riders risk improper tire inflation, affecting handling and control.

    Product
    BMW — BMW R 1250 RS, R 1250 RT, R 1250 R, R 1250 GS ADVENTURE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1538-2020·2020-08-19

    Itech 361 LLC Recalls All Clean Hand Sanitizer Due to Methanol

    Itech 361 LLC is recalling 18,760 bottles of All Clean Hand Sanitizer because the product contains undeclared methanol.

    Product
    All Clean Hand Sanitizer, Fresh Scent, 1 Liter bottles, Ethyl Alcohol 70.00%, Produced by Eskbiochem SA de CV Ave Mexico Japon 50 Celaya, Gto. Mexico 38010, Distributed by All Clean Natural LTD, UPC Code 6 28055 37013 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1147-2020·2020-08-19

    Wellements Iron Drops Recalled for Undeclared Milk Allergen

    Wellements LLC is recalling Iron Drops liquid dietary supplements because they contain undeclared milk. Consumers with milk allergies should not use the product.

    Product
    Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual product carton that includes a 1 mL oral syringe dispenser.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1149-2020·2020-08-19

    Upspring Baby Iron Supplement Recalled for Undeclared Milk

    Upspring, Ltd. is recalling 10,328 units of UpSpring Baby Iron + Immunity dietary supplements because they may contain undeclared milk.

    Product
    UpSpring Baby Iron + Immunity MULTI + IRON + ZINC Promotes nutrition For Healthy Growth + Immune System Support For Infants 4 months + Natural Grape Flavor Easy To Use Dropper Dietary Supplement NET WT 2 FL OZ (60 ML)UPC No: 859188006805 packaged in dark brown glass bottles and…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2795-2020·2020-08-19

    Bioseal Trachea Extenders Recalled for Stress Cracks and Leakage Risk

    Bioseal Corporation is recalling 900 units of Trachea Extenders due to stress cracks that may cause breathing system leakage, potentially preventing prescribed ventilation from reaching patients.

    Product
    Bioseal Trachea Extender 1/pl 50pk/Cs, REF TRAX01/50, LOT XXXX, STERILE EO, Single Use Only, Date of Manufacture XXXX, Expiration Date XXXX, LF, UDI: (01) 00630094916019 - Product Usage: Airway connectors intended to connect a breathing gas source to a tracheal tube…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1148-2020·2020-08-19

    Wellements Iron Drops Sampler Recalled for Undeclared Milk

    Wellements LLC is recalling Iron Drops Sampler liquid dietary supplements because the product contains undeclared milk.

    Product
    Iron Drops Sampler (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL, (2 mL fill) amber glass bottle packaged in an individual product carton that includes a 1 mL oral syringe dispenser.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E056000·2020-08-19

    Tong Yang Recalls Grille Mouldings for 2019-2020 Honda HR-V Vehicles

    Tong Yang is recalling aftermarket grille mouldings for 2019-2020 Honda HR-Vs because the coating may interfere with the Adaptive Cruise Control radar sensor, increasing crash risk.

    Product
    STRUCTURE:BODY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2780-2020·2020-08-19

    Maquet Holder HKHZ 19 Recalled for Insecure Oxygenator Fit

    Maquet is recalling Holder HKHZ 19 units for Quadrox-i and Quadrox-iD oxygenators because the holder may not securely hold the oxygenator.

    Product
    Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD Neonatal / Pediatric Oxygenators, Model Number: 701047495 - Product Usage: The Holder HKHZ 19 is an accessory to QUADROX i and QUADROX iD Neonatal / Pediatric oxygenator and is being used as a single holder for QUADROX i and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2775-2020·2020-08-19

    Luminex Verigene Processor SP Recalled for Potential False Negative Results

    Luminex is recalling Verigene Processor SP systems because an instrument failure may cause false negative results for Gram-positive and Gram-negative blood culture tests.

    Product
    Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product Usage: utilizes a single-use disposable test consumables and a self-contained Verigene Test Cartridge for each sample tested.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1495-2020·2020-08-19

    SCA Pharmaceuticals Recalls Heparin Sodium Bags Due to Low Potency

    SCA Pharmaceuticals is recalling 3,932 bags of Heparin Sodium 5,000 units due to out-of-specification potency results at the 30-day stability timepoint.

    Product
    Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL bag (5 units/mL), Rx only, SCA Pharmaceuticals 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0650-46
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·20V491000·2020-08-19

    2021 Keystone Outback travel trailers recalled for incorrect tire pressure label

    Keystone is recalling certain 2021 Outback travel trailers because the Federal Identification Tag incorrectly states tire pressure should be 65 PSI instead of the correct 80 PSI. Underinflated tires could fail and increase crash risk.

    Product
    KEYSTONE — KEYSTONE OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2773-2020·2020-08-19

    Ion Beam Applications Recalls Proteus 235 Proton Therapy Systems

    Ion Beam Applications is recalling four Proteus 235 Proton Therapy Systems because a software defect prevents users with long names from resuming interrupted treatments.

    Product
    Proteus 235 The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1501-2020·2020-08-19

    Eosera Recalls Ear Itch MD Sprays Due to Manufacturing Deviations

    Eosera, Inc. is voluntarily recalling specific lots of Ear Itch MD sprays nationwide due to cGMP deviations.

    Product
    Day & Night Pack Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%), 0.5 FL OZ (15 mL) bottles/Ear Itch MD Nighttime Intensive Soothing Spray (pramoxine HCL 1%), 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0071-5
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·20168·2020-08-19

    Hasbro Recalls Super Soaker XP 20 and XP 30 Water Blasters for Lead Content

    Hasbro is recalling Super Soaker XP 20 and XP 30 water blasters because decorative stickers contain lead levels exceeding federal bans. No injuries have been reported.

    Product
    Super Soaker XP 20 and Super Soaker XP 30
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2778-2020·2020-08-19

    Anjon Holdings Recalls Spinal Bone Fixation Fasteners Due to Galling

    Anjon Holdings is recalling 249 Anjon Bremer Molded Crown bone fixation fasteners because of a high rate of galling in a threaded component.

    Product
    Anjon Bremer Molded Crown. bone fixation fastener for spinal use. REF number 100048 - Product Usage: Smooth or threaded metallic bone fixation fastener. Provides cervical spine immobilization and therapeutic traction for treatment of patients with cervical trauma or other neck…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1500-2020·2020-08-19

    Eosera Recalls Ear Itch MD Anti-Itch Spray Due to cGMP Deviations

    Eosera, Inc. is voluntarily recalling 43,424 bottles of Ear Itch MD Anti-Itch Spray due to cGMP deviations. The product was distributed nationwide in the United States.

    Product
    Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0071-5, UPC 851722007125
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2770-2020·2020-08-19

    Ortho VITROS Anti-SARS-CoV-2 Reagent Recalled for Potential False Negatives

    Ortho Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 Total Reagent because swapped bottles may cause false negative or delayed results.

    Product
    VITROS Anti-SARS-CoV-2 Total Reagent, COV2TOT, VITROS CoV2T. Catalog number 6199922, UDI 10758750033386 - Product Usage: Rx ONLY. For in vitro diagnostic and Laboratory Professional use. For emergency authorization use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide