State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53726–53750 of 74002

SevereFDA (Devices)·Z-1609-2015·2015-06-03
CareFusion AVEA Ventilator Recalled for Pressure Transducer Failure
CareFusion is recalling AVEA ventilators because a pressure transducer failure can stop ventilation. Nonbreathing patients may require manual ventilation or a different device.
Product
CareFusion AVEA ventilator, all models. Product Usage: A continuous ventilator (respirator), intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·15V341000·2015-06-03
Toyota Recalls 2015 Lexus NX200t for ABS Actuator Defect
Toyota is recalling 3,013 2015 Lexus NX200t vehicles because a damaged ABS actuator component may cause loss of vehicle stability and increase crash risk.
Product
LEXUS — LEXUS NX200
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15E047000·2015-06-03
Advics Recalls Antilock Brake System Actuators Due to Contamination
Advics is recalling specific antilock brake system actuators manufactured in December 2014 due to contamination that may affect valve function and vehicle stability.
Product
SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1093-2015·2015-06-03
Advanced Physician Solutions Recalls Estradiol Cypionate Injectable Due to Sterility Concerns
Advanced Physician Solutions, Inc. is recalling Estradiol Cypionate injectable vials because the FDA determined there is a lack of assurance of sterility.
Product
ESTRADIOL CYPIONATE (SESAME OIL) 10ML, 30ML VIAL 5MG/ML INJECTABLE, Advanced Compounding Pharmacy, 7225 Fulton Ave., North Hollywood, CA 91605
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15E045000·2015-06-03
Timken Recalls Aftermarket Front Wheel Bearings for Ford, Mazda, Mercury
Timken is recalling aftermarket front wheel bearings with incorrect dimensions for 2001-2012 Ford Escape, 2001-2011 Mazda Tribute, and 2005-2011 Mercury Mariner vehicles due to crash risk.
Product
FORD — FORD, MAZDA, MERCURY ESCAPE, TRIBUTE, MARINER, TRIBUTE HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1103-2015·2015-06-03
Advanced Physician Solutions Recalls Sodium Hyaluronate Syringes Due to Sterility Concerns
Advanced Physician Solutions is recalling 416 prefilled syringes of Sodium Hyaluronate Injectable because the company cannot guarantee the product is sterile.
Product
SODIUM HYALURONATE (2ML PREFILLED SYRINGE) STERILE WATER 20MG/ML INJECTABLE, Advanced Compounding Pharmacy, 7225 Fulton Ave., North Hollywood, CA 91605
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15E046000·2015-06-03
Strange Engineering Recalls Modified Street Axles Due to Reduced Strength
Strange Engineering is recalling specific Modified Street Axles because post-manufacturing heat treatment may have reduced their strength, increasing the risk of axle failure and vehicle crashes.
Product
POWER TRAIN:AXLE ASSEMBLY:AXLE SHAFT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1097-2015·2015-06-03
Advanced Compounding Pharmacy Recalls Glycerin Injectable Due to Sterility Concerns
Advanced Physician Solutions, Inc. is recalling Glycerin (Sterile Water) 100ml 71% Injectable vials nationwide due to a lack of assurance of sterility.
Product
GLYCERIN (STERILE WATER) 100ML 71% INJECTABLE, Advanced Compounding Pharmacy, 7225 Fulton Ave., North Hollywood, CA 91605
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V343000·2015-06-03
Daimler Trucks Recalls Freightliner, Sterling, and Thomas Built Buses for Fire Risk
Daimler Trucks is recalling 3,200 trucks and buses due to a defect that may allow engine oil to contact hot surfaces, increasing the risk of fire.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES, STERLING, FREIGHTLINER SAF-T-LINER HDX, LT8500, M2, 114SD
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1098-2015·2015-06-03
Advanced Physician Solutions Recalls Hydroxyprogesterone Caproate Injectable Due to Sterility Concerns
Advanced Physician Solutions is recalling Hydroxyprogesterone Caproate injectable vials because the company cannot ensure the product is sterile.
Product
HYDROXYPROGESTERONE CAPROATE (OLIVE OIL) 30ML, 10ML VIAL 250MG/ML INJECTABLE, Advanced Compounding Pharmacy, 7225 Fulton Ave., North Hollywood, CA 91605
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1691-2015·2015-06-03
Biosense Webster Recalls SMARTABLATE RF Generator Systems Due to Unintended Energy Delivery
Biosense Webster is recalling 115 SMARTABLATE RF Generator Systems because two complaints reported the device inadvertently delivered RF energy during procedures.
Product
SMARTABLATE RF Generator System, Catalog No. M490006, M490007, M4900106, and M4900107. Product Usage: The use of the SMART ABLATE Generator and all accessories is indicated in combination with compatible therapeutic catheters for use in conventional intracardiac RF ablation…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1688-2015·2015-06-03
Terumo Advanced Perfusion System 1 Base Recalled for Power Loss
Terumo is recalling 1,713 Advanced Perfusion System 1 bases worldwide to address power loss issues. The recall involves design changes and switch protectors.
Product
Base for Terumo Advanced Perfusion System 1, 220/240V The Terumo¿ Advanced Perfusion System 1 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1678-2015·2015-06-03
Halyard KimVent Closed Suction System Recalled for Potential Valve Defect
Halyard Health is recalling specific KimVent Turbo-Cleaning Closed Suction Systems for adults because a defective internal valve may allow air to leak from the ventilator circuit.
Product
KimVent Turbo-Cleaning Closed Suction System for Adults, 10 F T-Piece (Product Code 227105); KimVent Turbo-Cleaning Closed Suction System for Adults, 12 F, DSE (Product Code 2271603); KimVent Turbo-Cleaning Closed Suction System for Adults, 12 F, T-Piece (Product Code 227135).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1684-2015·2015-06-03
Codman 3000 Series Refill Set Recalled for Leaking Needles
Codman & Shurtleff, Inc. is recalling 5,463 units of the CODMAN 3000 Series Refill Set because the needles may leak from the hub connection.
Product
CODMAN 3000 Series Refill Set- Huber needles. Used in combination with the CODMAN 3000 Series Constant Flow Implantable Pump CATALOG NO. : AP-07014 Each CODMAN 3000 Refill Kit contains 2 (two) 22 Gauge x 1.5 Huber Point Needles which are used in conjunction with a 50 mL…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V342000·2015-06-03
Volvo Recalls 2016 XC90 Vehicles for Side Air Bag Wiring Defect
Volvo is recalling 2016 XC90 vehicles because incorrect side air bag wiring may disable the safety feature, increasing injury risk in a crash.
Product
VOLVO — VOLVO XC90
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1681-2015·2015-06-03
Medtronic Recalls SynchroMed II Implantable Pumps Due to Alarm Failure
Medtronic is recalling specific SynchroMed II implantable drug pumps because the audible alarm may stop working, potentially preventing patients from detecting issues.
Product
Medtronic SynchroMed II Implantable Infusion Pumps, models 8637-20 and 8637-40. Sterile. Product Usage: The implantable Medtronic SynchroMed II programmable pumps are part of an infusion system that stores and delivers a prescribed drug to a specific site. The implanted…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1677-2015·2015-06-03
Alere i Influenza A & B kits recalled for false negative risk
Alere Scarborough, Inc. is recalling specific lots of Alere i Influenza A & B kits due to a high invalid rate and increased risk of false negative results.
Product
Alere i Influenza A & B Product Usage: The Alere i Influenza A and B assay, performed on the Alere i Instrument, is a rapid molecular in vitro diagnostic test utilizing an isothermal nucleic acid amplification technology for the qualitative detection and discrimination of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1689-2015·2015-06-03
Maquet Quadrox-iD Adult Diffusion Membrane Oxygenator Recalled for Blood Leakage Risk
Maquet Cardiovascular is recalling Quadrox-iD Adult Diffusion Membrane Oxygenators due to a potential issue that could result in blood leakage from the gas outlet port.
Product
Quadrox-iD Adult Diffusion Membrane Oxygenator Product Usage: The Quadrox-iD Adult Diffusion Membrane Oxygenator is intended for use in an extracorporeal circulation during cardiopulmonary bypass in cardiac surgery. Within the specified flow rate range, the device oxygenates…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1679-2015·2015-06-03
RaySearch RayStation Software Recalled for Dose Calculation Errors
RaySearch Laboratories AB is recalling RayStation software versions 2.5 through 4.0 due to dose calculation issues in specific VMAT plans.
Product
RaySearch RayStation 2.5, 3.0, 3.5 and 4.0; Radiation Therapy Treatment Product Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1671-2015·2015-06-03
Stryker EliteCore Biopsy Device Recalled for Cannula Overthrow Risk
Stryker is recalling EliteCore Full Core Biopsy Devices because the cannula may extend past its intended length.
Product
EliteCore Full Core Biopsy Device. EliteCore 18G, 20cm with and without HiLiter tip, 15 cm with and without HiLiter tip, and 10 cm with and without HiLiter tip.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1672-2015·2015-06-03
DePuy LCS COMPLETE RPS Femoral Implants Recalled for Patello-femoral Pain Risk
DePuy Orthopaedics is recalling 19,059 LCS COMPLETE RPS Femoral Implants because they are associated with higher revision rates and potential patello-femoral pain when the native patella is not resurfaced.
Product
LCS COMPLETE RPS Femoral Implants, various sizes and orientation. Knee prosthesis component for orthopedic surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1673-2015·2015-06-03
DePuy LCS Knee Prosthesis Recalled for Higher Revision Rates
DePuy Orthopaedics is recalling LCS COMPLETE RPS knee inserts because they show higher revision rates in Australia when the patella is not resurfaced.
Product
LCS COMPLETE RPS inserts, various sizes. Knee prosthesis component for orthopedic surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1683-2015·2015-06-03
OptiMedica Catalys Precision Laser System Software Recall for Incorrect Parameters
OptiMedica is recalling Catalys Precision Laser Systems with software version 3.00.05 because a software anomaly may provide incorrect cataract surgery parameters.
Product
Catalys Precision Laser System-Catalys - U - US product; Catalys-1 - International product; software version 3.00.05 The OptiMedica Catalys Precision Laser System is indicated for use in patients undergoing cataract surgery for removal of the crystalline lens.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1680-2015·2015-06-03
GE Healthcare Recalls D-Fend Water Traps Due to Occlusion Risk
GE Healthcare is recalling D-Fend and D-Fend+ water traps because they may occlude, causing a loss of respiratory gas monitoring.
Product
D-fend, (p/n 876446-HEL), and D-fend+ (p/n 881319-HEL) water trap. Used with Compact Airway Modules E/M-C(Ai)O(V)(X) and Cardiocap/5 monitors. Product Usage: Water traps are intended to protect the GE monitor from humidity, secretions and bacterial contamination when…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1686-2015·2015-06-03
Medrad Stellant CT Injector System Recalled for Under-Volume Hazard
Medrad Inc dba Bayer R&I is recalling 133 Stellant CT Injector Systems with Certegra Workstations due to a configuration error that may cause under-infusion of contrast media.
Product
MEDRAD¿ Stellant CT Injector System with Certegra Workstation; intended for the specific purpose of injecting intravenous contrast media into humans for diagnostic studies in computed tomography (CT) applications.
Category
Medical Device
Distribution
Distributed nationwide