The Recall Desk

State

US Virgin Islands product recalls

73,509 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
39
Most recent
2026-10-14

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 39 (22%) are Severe.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25376–25400 of 73686

  • HighCPSC·21736·2021-04-08

    GEO Essential Oils Recalled for Non-Child-Resistant Packaging and Poisoning Risk

    Geo Essential LLC is recalling Wintergreen and Alleviate essential oils because the packaging is not child-resistant, posing a poisoning risk to young children.

    Product
    GEO Wintergreen Organic Essential Oil and GEO Alleviate Organic Essential Oil Blend
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0356-2021·2021-04-07

    Wilton Valentine Chip Crunch Sprinkles Recalled for Undeclared Milk

    Wilton Industries Inc. is voluntarily recalling 1,638 units of Valentine Chip Crunch Sprinkles nationwide due to undeclared milk.

    Product
    Wilton Valentine Chip Crunch Sprinkles, 3.46 oz (98g) clear plastic bottle, SKU 710-4277 UPC 070896042774
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0358-2021·2021-04-07

    Wilton Rainbow Chip Crunch Sprinkles Recalled for Undeclared Milk

    Wilton Industries is recalling Rainbow Chip Crunch Sprinkles nationwide due to undeclared milk, a major food allergen.

    Product
    Wilton Rainbow Chip Crunch Sprinkles, 5.25oz (148g) clear plastic bottle, SKU 710-9704 UPC 070896797049
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0360-2021·2021-04-07

    Wilton Holiday Home Treat Toppings Recalled for Undeclared Milk

    Wilton Industries is recalling Holiday Home Assorted Treat Toppings nationwide due to undeclared milk, a major allergen.

    Product
    Holiday Home Assorted Treat Toppings, 2.6oz (74g) 3 hanging clear plastic bags with 1 paperboard card, SKU 710-0-0207 UPC 041226473612
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1334-2021·2021-04-07

    CF Delivery Dev Caps Bravo x5 Recalled for Aspiration Risk

    FDA recalls CF Delivery Dev Caps Bravo x5 capsules because they may fail to attach to the esophagus, leading to aspiration.

    Product
    CF Delivery Dev Caps Bravo x5, FGS-0635/FGS 0636 - Product Usage: intended to be used for gastroesophageal pH measurement and monitoring of gastric reflux in adults and children from 4 years of age.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1259-2021·2021-04-07

    Smisson-Cartledge ThermaCor 1200 Disposable Sets Recalled for Aluminum Leaching Risk

    Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets due to a toxicological risk assessment indicating potential aluminum ion leaching into warmed fluids.

    Product
    ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge Biomedical ThermaCor 1200 Rapid Thermal Infusion System, used for infusion of: -crystalloid, colloid, or blood product, including packed red blood cells, as volume replacement for patients suffering from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1258-2021·2021-04-07

    ThermaCor 1200 Disposable Sets Recalled for Potential Aluminum Leaching

    Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets because a toxicological assessment found potential for aluminum ions to leach into warmed fluids.

    Product
    ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge Biomedical ThermaCor 1200 Rapid Thermal Infusion System, used for infusion of: -crystalloid, colloid, or blood product, including packed red blood cells, as volume replacement for patients suffering from blood…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1305-2021·2021-04-07

    Medtronic Recalls Implantable Cardioverter Defibrillators Due to Shortened Replacement Time

    Medtronic is recalling specific Evera and Visia ICD models because a small percentage may experience a shortened Recommended Replacement Time to End of Service interval.

    Product
    Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR, Evera S DR, Evera MRI XT DR, Evera MRI S DR, Evera XT VR, Evera S VR and Evera MRI S VR models; 2) Visia family: Visia AF ICD, Visia AF S ICD, Visia AF MRI ICD, and Visia AF MRI S ICD models.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1260-2021·2021-04-07

    ThermaCor 1200 Disposable Sets Recalled for Potential Aluminum Leaching

    Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets due to a toxicological risk assessment indicating potential aluminum ion leaching into warmed fluids.

    Product
    ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge Biomedical ThermaCor 1200 Rapid Thermal Infusion System, used for infusion of: -crystalloid, colloid, or blood product, including packed red blood cells, as volume replacement for patients suffering from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0316-2021·2021-04-07

    Zydus Recalls Acyclovir Sodium Injection Due to Crystallization

    Zydus Pharmaceuticals is recalling 1,638 packs of Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.

    Product
    ACYCLOVIR — ACYCLOVIR (ACYCLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1335-2021·2021-04-07

    FDA Recalls Bravo pH Capsule Delivery Devices Due to Aspiration Risk

    The FDA is recalling Bravo pH Capsule Delivery Devices because the capsule may fail to attach to the esophagus, leading to aspiration and potential hospitalization.

    Product
    BRAVO PH CAPS DELIVERY DEV5-PK, FGS-0312/FGS-0313 - Product Usage: intended to be used for gastroesophageal pH measurement and monitoring of gastric reflux in adults and children from 4 years of age.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·21104·2021-04-07

    Goal Zero Recalls EC8 Power Cables Due to Fire Hazard

    Goal Zero is recalling about 7,850 EC8 power cables because the connector pins can deform and overheat, posing a fire hazard. Four reports of overheating or fire have been received, with no injuries.

    Product
    EC8 Power Cables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0361-2021·2021-04-07

    Nuts.com Diced Dried Figs Recalled for Undeclared Almonds

    Nuts.com is recalling diced dried figs because they contain undeclared almonds, a major food allergen.

    Product
    Nuts.com brand Diced Dried Figs packaged in 1lb stand up gusset pouches.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0357-2021·2021-04-07

    Wilton Holiday Mix Sprinkles Recalled for Undeclared Milk

    Wilton Industries is recalling 18,740 units of Holiday Mix Sprinkles nationwide due to undeclared milk, a major food allergen.

    Product
    Wilton Holiday Mix Sprinkles, 7.6oz (215g) clear plastic bottle, SKU 710-7649 UPC 070896276490
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0355-2021·2021-04-07

    Wilton Rainbow Chip Crunch Sprinkles Recalled for Undeclared Milk

    Wilton Industries is recalling Rainbow Chip Crunch Sprinkles nationwide due to undeclared milk, a major food allergen.

    Product
    Wilton Rainbow Chip Crunch Sprinkles, 5.25 oz (148g) clear plastic bottle, SKU 710-5364 UPC 070896453648
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0359-2021·2021-04-07

    Wilton Autumn Sprinkles Recalled for Undeclared Milk Allergen

    Wilton Industries is recalling 8,742 units of Autumn Assorted Treat Toppings Sprinkles nationwide due to undeclared milk.

    Product
    Wilton Autumn Assorted Treat Toppings Sprinkles, 2.6oz (74g) 3 hanging clear plastic bags with 1 paperboard card, SKU 710-9722 UPC 070896097224
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1306-2021·2021-04-07

    Medtronic Recalls CRT-D Devices Due to Shortened Replacement Time

    Medtronic is recalling specific CRT-D implantable cardioverter defibrillators because a small percentage may experience a shortened time before the device reaches end of service.

    Product
    Implantable cardioverter defibrillators (ICD) with cardiac resynchronization therapy (CRT-D): 1) Viva family: Viva XT CRT-D, Viva XT Quad CRT-D, Viva S CRT-D, Viva Quad S CRT-D and Viva Quad C CRT-D models; 2) Claria family: Claria MRI CRT-D and Claria MRI Quad CRT-D models; 3)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1309-2021·2021-04-07

    CareFusion Recalls BD Alaris Infusion Pump Keypads Due to Fluid Ingress

    CareFusion is recalling BD Alaris Infusion Pump Module Keypads and Door Assembly Kits because fluid ingress can cause unresponsive or stuck keys, potentially delaying medication infusion.

    Product
    BD Alaris Infusion Pump Module Model 8100 Pump Module Keypad; and Pump Module Door Assembly Replacement Kit with Pump Module Keypad, Parts: 49000239; 49000346; 49000438; 49000439.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0315-2021·2021-04-07

    Zydus Recalls Acyclovir Sodium Injection Due to Crystallization

    Zydus Pharmaceuticals is recalling Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.

    Product
    ACYCLOVIR — ACYCLOVIR (ACYCLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V244000·2021-04-07

    New Flyer Recalls Electric Buses Due to Inverter Firmware Errors

    New Flyer is recalling certain 2013-2021 electric buses because firmware errors in the inverters may cause the electric drive system to shut down, increasing the risk of a crash.

    Product
    NEW FLYER — NEW FLYER XE60, XE35, XE40, XHE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1313-2021·2021-04-07

    Medtronic Bio-Console 560 Blood Pumping Console Recalled for Electrical Failure

    Medtronic is recalling Bio-Console 560 devices because an electrical component may fail, causing the pump to stop and potentially producing smoke or a burning odor.

    Product
    Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console, Model Numbers: 560BC, 560BC1, 560BCS, 560BCS1, R560BCS1. Used in cardiopulmonary bypass (CPB) procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V243000·2021-04-07

    Utility Trailer Recalls VS2DC, VS2DX, VS3DX Models for Missing Weld

    Utility Trailer is recalling 2006-2021 VS2DC, VS2DX, and VS3DX trailers because a missing weld may cause the slider rail to detach, increasing crash risk.

    Product
    UTILITY TRAILER — UTILITY TRAILER VS3DX, VS2DX, VS2DC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1323-2021·2021-04-07

    Nuvasive PRECICE STRYDE Intramedullary Nail Recall for Biological Safety Concerns

    Nuvasive Specialized Orthopedics is recalling PRECICE STRYDE intramedullary nails due to complaints of adverse events potentially related to biological safety, including pain and bony abnormalities.

    Product
    PRECICE STRYDE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
    Category
    Medical Device
    Distribution
    Distributed nationwide