The Recall Desk

State

US Virgin Islands product recalls

73,809 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45326–45350 of 73987

  • HighUSDA FSIS·pha-120916·2016-12-09

    Undercooked Chicken in Ready-to-Eat Products Recalled Nationwide

    USDA FSIS issued a public health alert for ready-to-eat chicken products that may be undercooked and incorporated into other foods. Consumers are urged not to consume these items.

    Product
    National Steak Processors (2024), LLC. — FSIS Issues Public Health Alert For Possibly Undercooked Ready-To-Eat Chicken Products That Have Been Incorporated Into Other Food Products
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V887000·2016-12-09

    Smeal Aerial Fire Apparatus Recalled for Guardrail Defect

    Smeal is recalling 216 aerial fire apparatus vehicles because a movable ladder access guardrail may bend or break under heavy loads, increasing injury risk.

    Product
    SMEAL — SMEAL AERIAL, AERIAL FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V888000·2016-12-09

    Honda Recalls 2017 Ridgeline AWD Vehicles for Wiring Harness Defect

    Honda is recalling 2017 Ridgeline AWD vehicles because water may enter the rear wiring harness, causing corrosion that could unexpectedly activate the stability assist system and increase crash risk.

    Product
    HONDA — HONDA RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17048·2016-12-08

    Masterbuilt and Cabela's 7-in-1 Gas Smokers Recalled for Fire Hazard

    Masterbuilt is recalling about 41,000 7-in-1 gas smokers because the PVC gas hose can disconnect, posing a fire hazard. Consumers should stop using the units and contact the manufacturer for a free replacement hose.

    Product
    Masterbuilt and Cabela's 7-in-1 gas smokers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V882000·2016-12-08

    Starcraft RV Recalls 2017 Mini Trailers With Incorrect Tire Labels

    Starcraft RV is recalling 125 model year 2017 mini trailers because federal labels may list incorrect tire and rim sizes, potentially leading to unsafe replacements.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AUTUMN RIDGE, COMET MINI, LAUNCH, SATELLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17047·2016-12-08

    Yankee Candle Recalls Luminous Candles Due to Glass Cracking Hazard

    Yankee Candle is recalling Luminous Collection candles because the glass jars can crack when lit, posing a laceration hazard. No injuries have been reported.

    Product
    Luminous Candle Collection
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·17718·2016-12-07

    Playworld Recalls Stainless Steel Playground Slides Due to Amputation Hazard

    Playworld is recalling about 1,300 stainless steel playground slides because a weld can crack, creating a space where a child's fingers can be caught and amputated.

    Product
    Lightning Slide stainless steel playground slide
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0550-2017·2016-12-07

    Island Soups Gungo Peas Soup Recalled for Botulism Risk

    Island Soups Company Inc. is recalling Gungo Peas Soup No Meat due to possible contamination with Clostridium botulinum.

    Product
    ISLAND SOUPS, GUNGO PEAS SOUP NO MEAT, NET WT. 16 OZ (28.4G)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0554-2017·2016-12-07

    Island Soups Fish Soup Recalled for Possible Botulism Contamination

    Island Soups Company Inc. is recalling Fish Soup due to possible contamination with Clostridium botulinum. The product was distributed nationwide via internet orders.

    Product
    ISLAND SOUPS, FISH SOUP, NET WT. 16 OZ (28.4G)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0553-2017·2016-12-07

    Island Soups Red Peas Soup Recalled for Botulism Risk

    Island Soups Company Inc. is recalling Red Peas Soup due to possible contamination with Clostridium botulinum. Consumers should check their pantry for affected cans.

    Product
    ISLAND SOUPS, RED PEAS SOUP, NET WT. 16 OZ (28.4G)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0551-2017·2016-12-07

    Island Soups Gungo Peas Soup Recalled for Botulism Risk

    Island Soups Company Inc. is recalling Gungo Peas Soup due to possible contamination with Clostridium botulinum. The product was distributed nationwide via internet orders.

    Product
    ISLAND SOUPS, GUNGO PEAS SOUP, NET WT. 16 OZ (28.4G)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0549-2017·2016-12-07

    Island Soups Mannish Water Recalled for Possible Botulism Contamination

    Island Soups Company Inc. is recalling Mannish Water soup due to possible contamination with Clostridium botulinum. Products were sold nationwide via internet orders.

    Product
    ISLAND SOUPS, MANNISH WATER, NET WT. 16 OZ (28.4G)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V879000·2016-12-07

    Heartland Landmark 365 Fifth Wheel Trailer Recall for Brake Line Wear

    Heartland is recalling 2016-2017 Landmark 365 fifth wheel trailers because the spare wheel may rub against the brake line, causing wear and potential loss of braking.

    Product
    HEARTLAND — HEARTLAND LANDMARK 365
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0552-2017·2016-12-07

    Island Soups Red Peas Soup Recalled for Botulism Risk

    Island Soups Company Inc. is recalling Red Peas Soup No Meat due to possible contamination with Clostridium botulinum.

    Product
    ISLAND SOUPS, RED PEAS SOUP NO MEAT, NET WT. 16 OZ (28.4G)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0559-2017·2016-12-07

    Purely Elizabeth Chocolate Sea Salt Probiotic Granola Recalled for Undeclared Soy

    Purely Elizabeth is recalling Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin, posing a risk to individuals with soy allergies.

    Product
    Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz, PET/LLDPE Pouch, 6 units/case,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0684-2017·2016-12-07

    MicroPort Dynasty Liners Recalled Due to Metal Debris Tissue Reaction Risk

    MicroPort Orthopedics is recalling 6,250 Dynasty Liners used in hip replacements due to an increasing trend of suspected tissue reactions to metal debris.

    Product
    Dynasty Liners: REF DLCOGA28, REF DLCOGB32, REF DLCOGC36, REF DLCOGD38, REF DLCOGE40, REF DLCOGF42, REF DLCOGG44, REF DLCOGH48, REF DLCOGJ52, REF DLCOGK56, For use with the conserve metal head
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0673-2017·2016-12-07

    Roche OMNI S Cassette Recall for Incorrect Urea Measurement Results

    Roche is recalling 97 MSS Cassette units for the OMNI S Analyzer due to a software error that may cause incorrect urea results, potentially delaying diagnosis of inborn disorders in children.

    Product
    MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche OMNI S Analyzer: cobas b 221<6>Roche OMNI S6 system The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0666-2017·2016-12-07

    Hamilton Medical Recalls MR1 Ventilators Due to Oxygen Tubing Loosening Risk

    Hamilton Medical is recalling 44 MR1 ventilators because the oxygen tubing and connector could become loose during preparation, potentially compromising ventilation support.

    Product
    Hamilton-MR1 Ventilator: Catalog# 161010 The Hamilton MR1 Ventilator is intended to provide pressure ventilator support to adults and pediatrics, and optionally infants and neonates. Intended areas of use include: MRI Dept., Intensive, intermediate, emergency and long-term…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0677-2017·2016-12-07

    Teleflex Recalls Arrow OnControl Bone Lesion Biopsy System Trays

    Teleflex Medical is recalling Arrow OnControl Bone Lesion Biopsy System trays due to a potential incomplete seal on the outer sterile package.

    Product
    ARROW OnControl Bone Lesion Biopsy System Tray, Sterile, Rx only, The Arrow OnControl Bone Lesion Biopsy System is intended for bone biopsy of the vertebral body and bone lesions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0154-2017·2016-12-07

    Par Pharmaceutical Recalls Travoprost Ophthalmic Solution Due to Sterility Concerns

    Par Pharmaceutical is recalling specific lots of Travoprost Ophthalmic Solution because the dropper tips may be damaged, compromising sterility.

    Product
    Travoprost Ophthalmic Solution USP, 0.004%, a) 2.5 mL and b) 5 mL bottles, Rx only, FOR USE IN THE EYES ONLY, Made in India, Distributed by: Par Pharmaceutical Cos., Inc, Spring Valley, NY 10977
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0665-2017·2016-12-07

    Merge Healthcare Recalls Hemo Software Due to Potential Application Crashes

    Merge Healthcare is recalling Merge Hemo software versions 9.10 through 9.40.2 because the application may crash during cardiac catheterization procedures.

    Product
    Merge Hemo software. Merge Hemo monitors, measures, and records physiologic data from a human patient undergoing a cardiac catheterization procedure. The Monitoring System is for the monitoring of vital parameters including ECG, SpO2, invasive blood pressure, temperature…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0690-2017·2016-12-07

    Domain Surgical Recalls FMsealer Open Shears Due to Jaw Fractures

    Domain Surgical is recalling FMsealer Open Shears (Model FM3001) because fixed jaw fractures were observed during clinical usage.

    Product
    FMsealer Open Shears. Model FM3001
    Category
    Medical Device
    Distribution
    Distributed nationwide