The Recall Desk

State

US Virgin Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51326–51350 of 73995

  • ModerateFDA (Devices)·Z-0231-2016·2015-11-11

    Ortho-Clinical VITROS 5,1 FS Chemistry System Software Recall

    Ortho-Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry Systems due to a software anomaly where user-modified parameters revert to default values during ADD installation.

    Product
    VITROS 5,1 FS Chemistry System, Catalog Number/Product Code 6801375, Unique Device Identifier No. 10758750001132, and VITROS 5,1 FS Chemistry System Refurbished, Catalog Number/Product Code 6801890, Unique Device Identifier No. 10758750001644. Intended for use in the in vitro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0214-2016·2015-11-11

    ELITech Eon 100 Reagents Recalled for Potential Drug Interference

    ELITech Clinical Systems is recalling Eon 100 reagents due to potential drug interference. No complaints have been received.

    Product
    Eon 100 system included the following product reference numbers and names: Reference no. 77345- Glucose (GPSL) Reference no. 77450- Uric acid (AUVD) Reference no. 77435- Triglycerides (TGML) Reference no. 77295- Cholesterol (CHVD) Reference no. 77301- Cholesterol HDL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0220-2016·2015-11-11

    Dako EnVision FLEX Visualization Reagent Recalled for Staining Defect

    Dako North America Inc. is recalling specific lots of EnVision FLEX visualization reagent kits due to a buffer defect causing non-specific background staining that interferes with result interpretation.

    Product
    EnVision FLEX/HRP visualization reagent found in the following kits: EnVision FLEX, High pH (Link) EnVision FLEX+, Mouse, High pH (Link) EnVision FLEX Mini Kit, High pH (Link) EnVision FLEX, High pH (Dako Omnis) Multi-component, sealed package. For in vitro diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0222-2016·2015-11-11

    Stryker UniVise Spinous Process Fixation Plate System Inserter Recalled

    Stryker Spine is recalling 41 units of the UniVise Spinous Process Fixation Plate System Inserter because the inner shaft does not fit through the device.

    Product
    Stryker UniVise Spinous Process Fixation Plate System Inserter, Stryker Spine, Non-Sterile. Reference Number 48590100. Manual Surgical Instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0215-2016·2015-11-11

    ELITech Eon 300 Reagents Recalled for Potential Drug Interference

    ELITech Clinical Systems is recalling Eon 300 reagents due to potential drug interference. No complaints have been received.

    Product
    Eon 300 system includes the following product reference numbers and names: Reference no. 79345 Glucose (GPSL) Reference no. 79450 Uric acid (AUVD) Reference no. 79435 Triglycerides (TGML) Reference no. 79295 Cholesterol (CHVD) Reference no. 79301 Cholesterol HDL (HDLL)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0217-2016·2015-11-11

    ELITech Envoy 500 Reagent Kits Recalled for Potential Drug Interference

    ELITech Clinical Systems is recalling Envoy 500 reagent kits due to potential drug interference. No complaints have been received.

    Product
    Envoy 500 system includes the following product reference numbers and names: 55345 ENVOY 500 Glucose 55450 ENVOY 500 URIC ACID REAGENT KIT 55435 ENVOY 500 TRIGLYCERIDES REAGENT KIT, 55297 ENVOY 500 CHOLESTEROL REAGENT KIT, 55335 ENVOY 500 CREATININE REAGENT KIT 55301…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0206-2016·2015-11-11

    Bausch + Lomb Recalls Biotrue ONEday Lenses Due to Surface Defects

    Bausch + Lomb is recalling Biotrue ONEday contact lenses because a manufacturing defect on the lens surface may cause visual disturbances like halos or poor vision.

    Product
    BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A), Product Order Number Biotrue SVS - 7201, STERILE, Rx Only; The lenses are available in 5 pack, 30 pack and 90 pack sizes; Biotrue ONEday Foil - Part Number 8098001, Biotrue ONEday 5 pack Carton International - Part Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0162-2016·2015-11-11

    Qualitest Recalls Ranitidine Syrup Due to Preservative Stability Failure

    Vintage Pharmaceuticals is recalling specific lots of Ranitidine Syrup because preservative levels failed stability specifications.

    Product
    RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION, USP) 15 mg/mL (75 mg/5 mL), 473 mL (16 fl oz), Rx only. Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC: 0603-9418-58.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0210-2016·2015-11-11

    Steris Recalls AMSCO Steam Sterilizers Due to Foot Pedal Software Issue

    Steris Corporation is recalling 32 AMSCO 400 and AMSCO C Small Steam Sterilizers because a software defect prevents the foot pedal from operating the door.

    Product
    AMSCO 400 and AMSCO C Small Steam Sterilizers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0202-2016·2015-11-11

    Ortho-Clinical VITROS Calibrator Kit 9 Recall for Wash Errors

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 9, Lot 0954, due to an increase in wash error condition codes.

    Product
    VITROS Chemistry Products Calibrator Kit 9 Calibrator, 2 mL, Product Code 8568040, Unique Device Identifier No. 10758750005031, IVD -- Ortho Clinical Diagnostics, Inc. --- VITROS Chemistry Products Calibrator Kit 9 is used to calibrate VITROS 250/350/950/5,1 FS and 4600…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0198-2016·2015-11-11

    C.R. Bard Recalls Antibacterial Hydro Personal Catheters Due to Labeling Error

    C.R. Bard is recalling 4,170 units of Antibacterial Hydro Personal Catheters because the unit label may incorrectly state the product code and size.

    Product
    Antibacterial Hydro Personal Catheter, Male 12 Fr, Product Code 63512, sold in boxes of 30 units
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V743000·2015-11-10

    Van Hool Recalls 2015-2016 Motorcoaches Due to Air Brake Defect

    Van Hool is recalling 48 model year 2015-2016 TD925 and TDX25 motorcoaches because air brakes may take too long to release, potentially causing brake drag, heat buildup, or fire.

    Product
    VAN HOOL — VAN HOOL TD925, TDX25
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V744000·2015-11-10

    Maserati Recalls 2016 GranTurismo Vehicles Due to Door Latch Defect

    Maserati is recalling 135 model year 2016 GranTurismo vehicles because passenger side door latches may not be heat treated, increasing injury risk in a crash.

    Product
    MASERATI — MASERATI GRANTURISMO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V746000·2015-11-10

    Spartan MetroStar and Defense Chassis Cabs Recalled for Axle Nut Issue

    Spartan Motors is recalling 2014-2015 MetroStar and Defense Department chassis cabs because improperly tightened axle nuts may cause the driveshaft to disconnect.

    Product
    SPARTAN — SPARTAN METROSTAR, DEFENSE DEPT. CHASSIS CAB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16028·2015-11-10

    Ignite Recalls Kids Straw Tumblers Due to Ingestion Risk

    Ignite USA LLC is recalling about 130,000 Bueno by Contigo Kids Straw Tumblers because small straw pieces can break off and be swallowed or inhaled by children.

    Product
    Bueno by Contigo Kids Straw Tumblers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V745000·2015-11-10

    Thor Motor Coach Recalls Motorhomes Due to Unstable Entry Steps

    Thor Motor Coach is recalling specific Damon, Four Winds, and Thor motorhomes because a bolt on the electric entry steps may fracture, causing the steps to become unstable and increasing the risk of injury.

    Product
    DAMON — DAMON, FOUR WINDS, THOR MOTOR COACH AVANTI, TUSCANY, CHALLENGER, DAYBREAK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16030·2015-11-10

    FontanaArte Recalls Sonmi Pendant Lamps Due to Falling Glass Shade Risk

    FontanaArte is recalling Sonmi pendant lamps because the glass shade can detach and fall, posing injury risks. Consumers should remove the shade and contact the company for repair.

    Product
    Sonmi pendant lamp light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V740000·2015-11-09

    Peterbilt Auto Haulers Recalled for Tire Speed Rating Mismatch

    PACCAR is recalling specific Peterbilt auto haulers because front tires have a lower speed rating than the vehicle's maximum speed, increasing crash risk.

    Product
    PETERBILT — PETERBILT 386, 348, 340, 337
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V739000·2015-11-09

    BMW Recalls 2014-2015 MINI Cooper Vehicles for Airbag Calibration Issue

    BMW is recalling 2014-2015 MINI Cooper and Cooper S vehicles because incorrectly calibrated seat sensors may cause inappropriate airbag activation or deactivation during a crash.

    Product
    MINI — MINI COOPER, COOPER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V741000·2015-11-09

    Forest River Surveyor Recalled for Incorrect Federal Certification Placard Tire Size

    Forest River is recalling 2010-2016 Surveyor recreational trailers because the Federal Certification Placard lists incorrect tire and rim sizes, which may lead to poor handling if incorrect tires are installed.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·139-2015·2015-11-07

    Cloverdale Foods Recalls Beef and Pork Bratwurst for Undeclared Milk Allergen

    Cloverdale Foods is recalling beef and pork bratwurst mislabeled as beef frankfurters because it contains undeclared milk, a known allergen.

    Product
    Cloverdale Foods Co. — Cloverdale Foods Company Recalls Beef and Pork Product Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V737000·2015-11-06

    Outdoors RV Recalls Trailers Due to Fire Risk from Pinched Wires

    Outdoors RV is recalling 2015-2016 Timber Ridge, Glacier Peak, Wind River, and Black Stone trailers because liquid propane hoses and electrical wires may be pinched or scraped, increasing the risk of fire.

    Product
    OUTDOORS RV — OUTDOORS RV TIMBER RIDGE, GLACIER PEAK, WIND RIVER, BLACK STONE
    Category
    Vehicle
    Distribution
    Distributed nationwide