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.

41201–41225 of 73919

  • HighNHTSA·17E050000·2017-09-07

    J-Tech Recalls Icon Alliance Motorcycle Helmets Due to Chin Strap Defect

    J-Tech is recalling specific Icon Alliance motorcycle helmets because faulty stitching may allow the chin strap to separate, increasing injury risk in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17220·2017-09-07

    Studio Fun International Recalls Slap Bracelets Sold with Storybooks

    Studio Fun International is recalling slap bracelets sold with DreamWorks Trolls storybooks because the metal band can wear through the fabric, posing a laceration hazard.

    Product
    Bracelets sold with storybooks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3476-2017·2017-09-06

    Amrita Apricot Strawberry Protein Bar Recalled for Listeria Contamination

    Amrita Health Foods is recalling Apricot Strawberry Protein Bars due to potential Listeria monocytogenes contamination. Consumers should check best-by dates and discard affected products.

    Product
    Amrita Apricot Strawberry Protein Bar, 50gm UPC :853009004056
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3467-2017·2017-09-06

    Grande Produce Recalls Papaya Cases Due to Salmonella Contamination

    Grande Produce is recalling 5,344 cases of Caribena yellow maradol papaya nationwide because the product is contaminated with Salmonella.

    Product
    Caribena yellow maradol papaya packed in 35 pound cases
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3477-2017·2017-09-06

    Amrita Pineapple Chia Energy Bar Recalled for Listeria Contamination

    Amrita Health Foods is recalling Pineapple Chia Energy Bars due to potential Listeria monocytogenes contamination. Consumers should check their pantry for affected products.

    Product
    Amrita Pineapple Chia Energy Bar, 50gm UPC: 853009004025
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3471-2017·2017-09-06

    Amrita Chocolate Maca Protein Bar Recalled for Listeria Contamination Risk

    Amrita Health Foods is recalling Amrita Chocolate Maca 15g Protein Bars due to potential Listeria monocytogenes contamination. Consumers should check best-by dates and stop eating the product.

    Product
    Amrita Chocolate Maca 15g Protein Bar, 60 gm UPC: 853009004056
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3478-2017·2017-09-06

    Amrita Apple Cinnamon Energy Bar Recalled for Listeria Contamination

    Amrita Health Foods is recalling 115,000 Apple Cinnamon Energy Bars nationwide due to potential Listeria monocytogenes contamination.

    Product
    Amrita Apple Cinnamon Energy Bar, 50gm UPC: 853009004049
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3472-2017·2017-09-06

    Amrita Dark Chocolate Quinoa Protein Bar Recalled for Listeria Risk

    Amrita Health Foods is recalling Dark Chocolate Quinoa 15g Protein Bars due to potential Listeria monocytogenes contamination.

    Product
    Amrita Dark Chocolate Quinoa 15g Protein Bar, 60gm UPC: 853009004438
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V553000·2017-09-06

    Seagrave Aerialscope Recall: Loose Tie Rods May Cause Loss of Steering

    Seagrave is recalling 2017 Aerialscope emergency vehicles because improperly torqued steer axle nuts may allow tie rods to loosen, risking a complete loss of steering.

    Product
    SEAGRAVE — SEAGRAVE AERIALSCOPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3474-2017·2017-09-06

    Amrita Chocolate Chip Coconut Protein Bar Recalled for Listeria Risk

    Amrita Health Foods is recalling 115,000 Chocolate Chip Coconut 15g Protein Bars nationwide due to potential Listeria monocytogenes contamination.

    Product
    Amrita Chocolate Chip Coconut 15g Protein Bar, 60gm UPC: 853009004391
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3475-2017·2017-09-06

    Amrita Mango Coconut Energy Bar Recalled for Listeria Contamination

    Amrita Health Foods is recalling 115,000 Mango Coconut Energy Bars nationwide due to potential Listeria monocytogenes contamination.

    Product
    Amrita Mango Coconut Energy Bar, 50gm UPC: 853009004018
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3479-2017·2017-09-06

    Amrita Cranberry Raisin Energy Bar Recalled for Listeria Contamination

    Amrita Health Foods is recalling Cranberry Raisin Energy Bars due to potential Listeria monocytogenes contamination. Consumers should check best-by dates and discard affected products.

    Product
    Amrita Cranberry Raisin Energy Bar, 50gm UPC: 853009004032
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·17217·2017-09-06

    Ameriwood Recalls Mainstays Chests of Drawers for Tip-Over Hazards

    Ameriwood Home is recalling about 1.6 million Mainstays chests of drawers because they can tip over or entrap children if not anchored to the wall.

    Product
    Mainstays chests of drawers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V554000·2017-09-06

    PACCAR Recalls Kenworth and Peterbilt Trucks Due to Steering Defect

    PACCAR is recalling specific Kenworth and Peterbilt trucks because a front axle sway bar link may detach and bind the steering system, increasing crash risk.

    Product
    PETERBILT — PETERBILT, KENWORTH 220, K370, 210, MODEL 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3473-2017·2017-09-06

    Amrita Sunflower Butter & Jelly Protein Bar Recalled for Listeria Risk

    Amrita Health Foods is recalling Sunflower Butter & Jelly 15g Protein Bars due to potential Listeria monocytogenes contamination.

    Product
    Amrita Sunflower Butter & Jelly 15g Protein Bar, 60gm UPC: 853009004414
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3093-2017·2017-09-06

    Siemens AXIOM Artis zee and Q/Q.zen X-ray Systems Recalled for Cooling Leak

    Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that could cause equipment failure.

    Product
    Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to , pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1125-2017·2017-09-06

    Morton Grove Recalls Amoxicillin and Clavulanate Potassium Oral Suspension

    Morton Grove Pharmaceuticals is recalling 7,332 bottles of Amoxicillin and Clavulanate Potassium Oral Suspension due to a customer complaint of a blue nitrile glove fragment found in the product.

    Product
    Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted) bottle, Rx Only, Manufactured By: Cipla Ltd. at Medispray Laboratories Pvt. Ltd., Kundaim Goa, India; Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3089-2017·2017-09-06

    Siemens AXIOM Artis zee and Q/Q.zen X-ray Systems Recalled for Cooling Leak

    Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US because a cooling system leak could cause equipment failure.

    Product
    Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to , pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3096-2017·2017-09-06

    Siemens AXIOM Artis zee and Q/Q.zen X-ray Systems Recalled for Cooling Leak

    Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that can cause equipment failure.

    Product
    Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to , pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17218·2017-09-06

    Kawasaki Recalls Brute Force 300 ATVs Due to Fuel Leak Fire Hazard

    Kawasaki is recalling about 20,000 Brute Force 300 ATVs because the fuel tap or carburetor can leak fuel, posing a fire hazard. No injuries have been reported.

    Product
    Brute Force 300 all-terrain vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3099-2017·2017-09-06

    Siemens AXIOM Artis zee and Q/Q.zen X-ray Systems Recalled for Cooling Leak

    Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that could cause equipment failure.

    Product
    Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to , pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3470-2017·2017-09-06

    Seven Sundays Muesli Recalled for Undeclared Almond Allergen

    Garden of Light Inc. is recalling Seven Sundays Vanilla Cherry Pecan Muesli because the product contains almonds but is labeled as containing only pecans.

    Product
    (a) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 12oz. pouch, UPC: 8-56088-00315-6 (b) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 2oz. cup UPC: 8-56088-00311-8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V549000·2017-09-06

    Keystone Recalls 2016-2018 Springdale and Summerland Trailers for Wiring Fire Risk

    Keystone RV Company is recalling 2016-2018 Springdale and Summerland recreational trailers because incorrectly connected wiring for electric stabilizer jacks can cause an electrical short and increase the risk of fire.

    Product
    KEYSTONE — KEYSTONE SUMMERLAND, SPRINGDALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3036-2017·2017-09-06

    NeuroLogica Recalls Samsung GU60A Digital X-ray Systems for Radiation Exposure

    NeuroLogica Corporation is recalling 87 Samsung GU60A digital X-ray systems because unintended areas are exposed to radiation during the Stitching function.

    Product
    Samsung GU60A system- Digital X-ray Imaging Systems are intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications
    Category
    Medical Device
    Distribution
    Distributed nationwide