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.

Which agencies issued them

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.

41176–41200 of 73919

  • SevereFDA (Drugs)·D-1130-2017·2017-09-13

    ImprimisRx Recalls Curcumin Emulsion Injection Due to Undeclared Excipient

    ImprimisRx is recalling Curcumin Emulsion 10mg/ml Injection vials because non-pharmaceutical grade PEG 40 Castor Oil was used due to supplier mislabeling.

    Product
    Curcumin Emulsion 10mg/ml Injection, Sterile 10 mL Multiple Dose Vial, For Slow IV Administration, Compounded for a licensed professional or patient use by ImprimisRx, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·17223·2017-09-13

    Target Recalls Room Essentials 4-Drawer Dressers for Tip-Over Hazards

    Target is recalling approximately 175,000 Room Essentials 4-drawer dressers due to tip-over and entrapment hazards that can result in death or injuries to children.

    Product
    Room Essentials 4-drawer dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3087-2017·2017-09-13

    Maquet CS 300 Intra-Aortic Balloon Pump Recalled for Fluid Ingress Risk

    Maquet Datascope is recalling CS 300 Intra-Aortic Balloon Pumps because fluid ingress could damage electronic boards, potentially preventing therapy initiation or continuation.

    Product
    CS 300 Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing coronary perfusion and reducing left ventricular work. Coronary perfusion is increased by augmenting blood pressure during the diastolic phase of the cardiac cycle. This increase in aortic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3110-2017·2017-09-13

    Elekta MOSAIQ Radiation Therapy System Recalled for Vertical Table Shift Error

    Elekta is recalling the MOSAIQ Medical Charged-Particle Radiation Therapy System because a software error inverts vertical table shifts, potentially directing therapy to incorrect areas.

    Product
    MOSAIQ Medical Charged-Particle Radiation Therapy System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1133-2017·2017-09-13

    ImprimisRx Recalls Timolol Ophthalmic Drops Due to Undeclared Excipient

    ImprimisRx is recalling compounded Timolol ophthalmic drops because they were made with non-pharmaceutical grade PEG 40 Castor Oil due to supplier mislabeling.

    Product
    Timolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic Drops, Sterile 5ml Bottle, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3113-2017·2017-09-13

    Beckman Coulter Hematology Analyzers Recalled for Potential Blast Detection Failure

    Beckman Coulter is recalling LH 750, LH 780, and LH 500 analyzers because they may fail to flag blasts in some blood samples.

    Product
    Coulter LH 750, Coulter LH 780, and Coulter LH 500 Analyzers Hematology Analyzers are quantitative, automated hematology analyzers and leukocyte differential counters For In Vitro Diagnostic used in clinical laboratories. They also provide automated Reticulocyte analysis and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3107-2017·2017-09-13

    Cardinal Health Recalls Presource Kits Contaminated with Needle Particulate

    Cardinal Health is recalling Presource surgical kits because they contained BD SafetyGlide needles with loose polypropylene particulate in the fluid path.

    Product
    Presource(R) Kits (custom surgical/procedural kits): The standard and custom kits are packed with all of the specific disposable class I, II, and II implantable, life-supporting, or life-sustaining devices required by customers for common surgical and other medical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V564000·2017-09-13

    Heartland Recalls 2018 Sundance XLT TT Trailers Due to Axle Defect

    Heartland is recalling 2018 Sundance XLT TT recreational trailers because rear axles were installed backwards, which may reduce braking ability or cause brakes to lock up.

    Product
    HEARTLAND — HEARTLAND SUNDANCE XLT TT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3114-2017·2017-09-13

    Beckman Coulter HmX Analyzers Recalled for Potential Blast Detection Failure

    Beckman Coulter is recalling HmX CP and HmX AL analyzers because they may fail to flag or detect blasts in rare blood sample situations.

    Product
    Coulter HmX CP and Coulter HmX AL Analyzers The purpose of the HmX Hematology Analyzer is to separate the normal patient, with all normal system-generated parameters, from the patient who needs additional studies. These studies include further measurements of cell size and cell…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3105-2017·2017-09-13

    Merge Unity Software Recall for Incorrect Gail Risk Calculations

    Merge Healthcare is recalling Merge Unity software versions 10.0 through 11.1.2 Patch 4 because the software fails to identify atypical hyperplasia, leading to incorrect Gail Risk calculations.

    Product
    Merge Unity software, formerly known as DR Systems Unity PACS software. The firm name on the label is Merge Healthcare, Hartland, WI. Merge Unity is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3112-2017·2017-09-13

    Qualigen Vitamin D Immunoassay Kit Recalled for Inaccurate Test Results

    Qualigen Inc is recalling specific lots of its Vitamin D Complete Immunoassay Kit because they may produce falsely low results.

    Product
    Qualigen(R) The FastPack(R) IP Vitamin D Complete Immunoassay Kit, catalog number 25000068 Vitamin D immunoassay kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1131-2017·2017-09-13

    ImprimisRx Recalls Latanoprost Ophthalmic Drops Due to Undeclared Excipient

    ImprimisRx is recalling 19 bottles of compounded Latanoprost ophthalmic drops because they contain non-pharmaceutical grade PEG 40 Castor Oil due to supplier mislabeling.

    Product
    Latanoprost PF Solution, 0.005%, Ophthalmic Drops in Sterile 5ml Bottles, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1132-2017·2017-09-13

    ImprimisRx Recalls Timolol-Latanoprost Ophthalmic Drops Due to Mislabeling

    ImprimisRx is recalling 16 bottles of compounded Timolol-Latanoprost ophthalmic drops because non-pharmaceutical grade PEG 40 Castor Oil was used due to supplier mislabeling.

    Product
    Timolol-Latanoprost PF Solution (0.5-0.005)%, Ophthalmic Drops, Sterile 5ml Bottle, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1127-2017·2017-09-13

    Lupin Recalls Famotidine Oral Suspension Due to Manufacturing Deviations

    Lupin Pharmaceuticals is recalling 12,888 bottles of Famotidine for Oral Suspension due to CGMP deviations. The FDA classified this voluntary recall as Class III.

    Product
    FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V562000·2017-09-12

    RAM Trucks Recalled for Water Pump Leak Fire Risk

    Chrysler is recalling 2013-2017 RAM trucks with specific Cummins diesel engines because a water pump defect may leak coolant and increase the risk of an engine compartment fire.

    Product
    RAM — RAM 2500, 3500, 4500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V561000·2017-09-12

    Highland Ridge Recalls 2018 Open Range 3X Trailers for Tire Labeling

    Highland Ridge RV is recalling 2018 Open Range 3X fifth wheel trailers because tire size labels may be incorrect, potentially leading to the installation of wrong-sized tires.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW OPEN RANGE 3X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17T015000·2017-09-11

    Trek Tire Recalls Dunlop GrandTrek PT3A Tires for Missing DOT Markings

    Trek Tire is recalling specific Dunlop GrandTrek PT3A tires manufactured in December 2016 because they lack complete DOT identification markings, which may increase crash risk.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V558000·2017-09-08

    Micro Bird Recalls 2016 G5 School Buses for Seat Safety Defect

    Micro Bird is recalling 25 units of 2016 G5 school buses because seat mounting studs may lack adequate padding, increasing injury risk in rear-end collisions.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17222·2017-09-08

    Nantucket Distributing Recalls Bimini Patio Set Chairs Due to Fall Hazard

    Nantucket Distributing is recalling Bimini patio set chairs because the fabric seat can tear, posing a fall hazard. Consumers should stop using the chairs and return them for a refund.

    Product
    Chairs sold with Bimini patio sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V557000·2017-09-07

    Eldorado Axess Transit Buses Recalled for Front Suspension Defect

    Eldorado is recalling 2015 Axess transit buses because front suspension link rod clamps may not be properly torqued, which can loosen the link rod and decrease steering ability.

    Product
    ELDORADO — ELDORADO AXESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V555000·2017-09-07

    Thor Motor Coach Recalls 2014-2016 Motorhomes for Wiper Defect

    Thor Motor Coach is recalling 2014-2016 motorhomes because windshield wipers may fail due to incorrect installation, increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR, THOR MOTOR TUSCANY XTE, DAYBREAK, ACE, MIRAMAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V556000·2017-09-07

    KZRV Recalls 2017-2018 Trailers Due to Missing Awning Light Fuse

    KZRV is recalling 2017-2018 Connect, Spree, and Sport Trek trailers because a missing fuse in the awning light circuit may cause wire overheating and fire.

    Product
    KZRV — KZRV CONNECT, SPREE, SPORT TREK
    Category
    Vehicle
    Distribution
    Distributed nationwide