State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

61301–61325 of 74011

ModerateFDA (Devices)·Z-0029-2014·2013-10-30
OPTI LION E-Plus Cassettes Recalled for Incorrect Barcode Labeling
OPTI Medical Systems is recalling OPTI LION E-Plus Cassettes because incorrect barcodes may affect performance over time and cause quality control failures.
Product
Model BP7507 OPTI LION E-Plus Cassettes 25 Cassettes with Sample Probes, OPTIMedical Cassettes are consumable used in the OPTI LION Electrolyte Analyzer intended to be used for the measurement of sodium, potassium, chloride, ionized calcium and pH in samples of whole blood…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0046-2014·2013-10-30
Abbott STAR Excimer Laser Systems Recalled for Thyristor Component Failure
Abbott Medical Optics is recalling STAR Excimer Laser Systems due to a thyristor failure on the power distribution board that affects the lamp and illumination system.
Product
STAR Excimer Laser System, Model: STAR S2, Catalog Number: 0030-1479, Product is manufactured and distributed by AMO Manufacturing USA, LLC, Milpitas, CA The STAR Excimer Laser Systems are indicated for laser assisted in situ keratomileusis (LASIK), photorefractive…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0031-2014·2013-10-30
Aesculap Recalls UNITRAC Pneumatic Retraction Arms Due to Safety Instructions
Aesculap, Inc. is recalling 217 UNITRAC Pneumatic Retraction Arms because updated instructions for use are required to ensure safe operation and extend product life.
Product
UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0066-2014·2013-10-30
GE Brivo C-Arm X-Ray Recalled for High Voltage Cable Failure
GE is recalling 29 Brivo C-Arm X-ray units because high voltage cable wires may fail, causing loss of system functionality.
Product
GE Brivo OEC715/785/865 C-Arm, Models: 715 Prime, 785 Essential, and 865 Plus. The QEC Brivo Mobile C-Arm X-Ray Products are designed to provide digital spot film imaging and fluoroscopic image guidance for all adult and pediatric populations for orientations between patient…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0054-2014·2013-10-30
Integra Licox Brain Tissue Oxygen Monitoring Kits Recalled for Defective Hex Wrench
Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring kits because a hex wrench may fail to loosen the set screw on the drill bit.
Product
Integra Licox Brain Tissue Oxygen Monitoring; 1 x Complete Brain Probe Kit REF IP1.P Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive Plainsboro, NJ…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0057-2014·2013-10-30
Integra Licox Brain Tissue Oxygen Monitoring Kits Recalled for Defective Hex Wrench
Integra LifeSciences is recalling 109 Licox Brain Tissue Oxygen Monitoring Kits because some contain a hex wrench that may fail to loosen the set screw on the drill bit.
Product
Inegra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Tunneling Probe Kit REF IT2 Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0059-2014·2013-10-30
Integra Licox Brain Tissue Oxygen Monitoring Kits Recalled for Defective Hex Wrench
Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring Kits because some contain a hex wrench that may fail to loosen the set screw on the drill bit.
Product
Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Probe Kit REF IM1.S Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive Plainsboro…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0061-2014·2013-10-30
Integra Licox Brain Tissue Oxygen Monitoring Kits Recalled for Defective Hex Wrench
Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring Kits because some lots contain a hex wrench that may not loosen the set screw on the drill bit.
Product
Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Introducer Kit REF IM2.S_.EU Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0064-2014·2013-10-30
DePuy SmartSet GMV Endurance Gentamicin Bone Cement Recalled for Uncleared Indications
DePuy Orthopaedics is recalling SmartSet GMV Endurance Gentamicin Bone Cement because it is intended for uses not cleared by the FDA.
Product
SmartSet¿ Endurance GMV, Gentamicin, REF 3105-040, Medium Viscosity Antibiotic Bone Cement, Sterile. SmartSet GMV Endurance Gentamicin, bone cements are self-curing, radiopaque, polymethyl methacrylate based cements, containing antibiotic, used for securing a metal or…
Category
Medical Device
Distribution
2 states
ModerateFDA (Devices)·Z-0033-2014·2013-10-30
Philips MRI Systems Recalled for Potential Water Freezing in Venting System
Philips Medical Systems is recalling 511 MRI systems because water may collect and freeze in the vent pipe, potentially blocking the magnet venting system.
Product
Philips MR Systems: Asset 0.5T, Apollo 0.5T, Infinion 1.5T, Eclipse/Polaris 1.5T, Panorama 0.6T 1.0T, Magnetic Resonance Imaging Systems intended for clinical/radiologic diagnostic imaging applications.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0035-2014·2013-10-30
Agfa IMPAX 5.2 DB Server Software Recall for Performance Issues
Agfa Corp. is recalling IMPAX 5.2 DB Server software because older versions may cause system downtime or slow performance in medical imaging systems.
Product
IMPAX 5.2 DB Server (running Oracle 10.1.0.4.0), medical imaging Picture Archiving and Communication System (PACS).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0063-2014·2013-10-30
Integra Licox Brain Tissue Oxygen Monitoring Kits Recalled for Defective Hex Wrench
Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring Kits because a hex wrench may fail to loosen the set screw on the drill bit.
Product
Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Probe Kit REF IM3.ST_.EU Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0062-2014·2013-10-30
Integra Licox Brain Tissue Oxygen Monitoring Kit Recall for Defective Hex Wrench
Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring Kits because some contain a hex wrench that may fail to loosen the set screw on the drill bit.
Product
Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Probe Kit REF IM3.S_.EU Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0056-2014·2013-10-30
Integra Licox Brain Tissue Oxygen Monitoring Kits Recalled for Hex Wrench Defect
Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring Kits because some hex wrenches may fail to loosen the set screw on the drill bit.
Product
Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Probe Kit REF IP2.P Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive Plainsboro, NJ…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0065-2014·2013-10-30
Varian Medical Recalls Breast Template System Due to Sterilization Defect
Varian Medical Systems is recalling 3 sets of the VARISOURCE Breast Template System because the templates may bend and turn opaque after steam sterilization.
Product
VARISOURCE Breast Template System for high-dose rate Brachytherapy. ***INSTRUCTIONS FOR USE*** Breast Bridge & Template System AL13011000 ***Manufacturer: Varian Medical Systems, Inc., 3100 Hansen Way, Palo Alto, CA 94304 USA
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0053-2014·2013-10-30
Alere Triage TOX Drug Screen Control 1 Recalled Due to Code Chip Failure
Alere San Diego, Inc. is voluntarily recalling Alere Triage TOX Drug Screen Control 1 because a provided code chip causes the control to fail in QC Sample Mode.
Product
Alere Triage¿ TOX Drug Screen Control 1 Product Generic Name: Quality Control Material Description of the product: Good Laboratory Practice suggests that external controls should be tested with each new lot or shipment of test materials, or every 30 days, and as…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-66402-001·2013-10-30
Tolmar Recalls Subpotent Ketoconazole Shampoo Nationwide
Tolmar Inc. is voluntarily recalling 391,055 bottles of 2% Ketoconazole Shampoo nationwide because the product was found to be subpotent.
Product
Ketoconazole Shampoo, 2%, Manufactured by TOLMAR Inc., Fort Collins, CO for Sandoz Inc., Princeton, NJ --- NDC 0781-7090-04.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0043-2014·2013-10-30
Advanced Sterilization Products Recalls STERRAD 200 Sterilizers for Odor Emission
Advanced Sterilization Products is recalling STERRAD 200 Sterilizers because they may emit unusual odors into the surrounding environment.
Product
STERRAD 200 Sterilizer (Single Door), Part Number: 10201. STERRAD 200 Sterilizer (Double Door), Part Number: 10202. The STERRAD Sterilization System is a low temperature general purpose sterilizer used to sterilize heat and moisture sensitive reusable medical devices.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·13V489000·2013-10-29
Hyundai Recalls 2009-2012 Genesis Vehicles for Brake Fluid Defect
Hyundai is recalling 2009-2012 Genesis vehicles because the brake fluid may not protect against corrosion of the Hydraulic Electronic Control Unit (HECU). This corrosion could reduce brake effectiveness and increase the risk of a crash.
Product
HYUNDAI — HYUNDAI GENESIS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·13V534000·2013-10-29
Prevost Recalls 2008-2009 Coach Buses Due to Battery Cable Fire Risk
Prevost is recalling 142 model year 2008-2009 X3-45 and X3-45 Entertainer coach buses because a battery cable may rub against a clamp, causing a short circuit and potential vehicle fire.
Product
PREVOST — PREVOST XLII-45 ENTERTAINER, X3-45
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·13V530000·2013-10-29
Setra Recalls Coaches Due to Electrical Fire Risk
Setra is recalling specific model year coaches because a battery component may conduct electricity and cause a fire.
Product
SETRA — SETRA S407 CC, S417, S417 TC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·13V532000·2013-10-29
Prevost Recalls 81 Coaches Due to Accelerator Pedal Spring Defect
Prevost is recalling 81 model year 2008-2010 coaches because broken accelerator pedal springs may prevent the pedal from returning to idle, increasing crash risk.
Product
PREVOST — PREVOST XLII-45 ENTERTAINER, H3 VIP, X3-45, H3-41
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·14007·2013-10-29
BreathableBaby Recalls Infant Wearable Blankets Due to Choking Hazard
BreathableBaby is recalling specific infant wearable blankets because zipper parts can detach and pose a choking risk. No injuries have been reported.
Product
BreathableSack wearable blanket for infants
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·14006·2013-10-29
Target Recalls Circo Children's Sitting Stools Due to Fall Hazard
Target is recalling about 69,000 Circo-brand Chloe and Conner sitting stools because the stabilizing bar can crack, causing the stool to collapse and posing a fall hazard to children.
Product
Circo-brand Chloe and Conner Sitting Stools
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·14701·2013-10-29
Honda Recalls 2012-2013 FourTrax Foreman ATVs Due to Steering Shaft Breakage
American Honda is recalling 21,000 2012 and 2013 FourTrax Foreman ATVs because the steering shaft can break, causing loss of control and crashes.
Product
All-terrain vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide