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.

60976–61000 of 74011

HighFDA (Devices)·Z-0184-2014·2013-11-20
Fresenius Hemodialysis Blood Lines Recalled for Potential Disconnection Risk
Fresenius Medical Care is recalling 8,528 cases of 2008K@ Home Blood lines due to a risk of disconnection and blood loss if not tightened correctly.
Product
2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis use Catalog Number: 03-2962-3. Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0201-2014·2013-11-20
Toshiba Titan 3T MRI System Recalled for SAR Display Error
Toshiba is recalling 18 Titan 3T MRI systems because they may display lower Specific Absorption Rate (SAR) values than actual when used with specific coils.
Product
Titan 3T MRI System, MRT-3010A/5. Product Usage: Usage: MRI system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0278-2014·2013-11-20
Medtronic RestoreUltra and RestoreSensor Neurostimulators Recalled for Loss of Stimulation
Medtronic is recalling 64,163 RestoreUltra and RestoreSensor neurostimulators worldwide due to a risk of loss of stimulation when switching program groups.
Product
Medtronic RestoreUltra, model 37712, and RestoreSensor, model 37714, Multi-program Rechargeable Neurostimulator for Spinal Cord Stimulation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0182-2014·2013-11-20
Urologix Recalls Prostiva RF Therapy Hand Piece Kits Due to Deployment Force Issue
Urologix is recalling 142 Prostiva RF Therapy Hand Piece Kits because the hand piece deployment force exceeded maximum specifications.
Product
Prostiva RF Therapy Hand Piece Kit, REF 8929, Rx only, sterilized using Ethylene Oxide. The Prostiva RF Model 8929 Hand Piece Kit is the delivery system component of the Prostiva RF Therapy System. Prostiva RF Therapy delivers low-levels of radiofrequency (RF) energy directly…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0192-2014·2013-11-20
DePuy Mitek FMS Outflow Tubing Recalled Due to Valve Malfunction
DePuy Mitek is recalling FMS Outflow Tubing because the pillow valve may not perform as intended, potentially leading to backflow of irrigation fluid and patient cross-contamination.
Product
DePuy Mitek FMS Outflow Tubing with One-Way valve Product Code:284649 Product Usage: The Intermediary Tubing for FMS¿ Fluid Management Systems connects the Inflow Tubing to the arthroscopic sheath during arthroscopic procedures. The Polyvinyl Chloride (PVC) tubing…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0284-2014·2013-11-20
Hospira Recalls Plum A+ Infusion Systems Due to Broken Pressure Sensor Pin
Hospira is recalling 10,669 Plum A+ Infusion Systems because the distal pressure sensor pin may break. This defect can prevent the device from detecting occlusions in the administration set.
Product
The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+ Infusion System is designed to deliver parenteral, enteral, or epidural infusions…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0275-2014·2013-11-20
DeRoyal Surgical Eye Spears Recalled for Incorrect X-Ray Detectability Labeling
DeRoyal Industries is recalling one lot of Surgical Eye Spears because they were labeled as x-ray detectable but contained non-detectable product.
Product
DeRoyal (R) Surgical Eye Spears, REF 30-049, Sterile EO, Manufacturer: DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849, MADE IN GUATEMALA cleaning of fluids from surgical site in or near the eye
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0282-2014·2013-11-20
Draeger Ceiling Supply Units Recalled Due to Broken Drive Screw
Draeger Medical is recalling 139 Movita 603x/DVE 803x Ceiling Supply Units because a broken drive screw caused the lift arm to fall.
Product
Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended for use in operating theaters and intensive care
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0270-2014·2013-11-20
GE Healthcare Recalls AW Workstations Due to Image Orientation Error
GE Healthcare is recalling AW VolumeShare and AW Server software due to a potential safety issue where images may display in the wrong orientation after rotation.
Product
AW VolumeShare 4 (ADVANTAGE WORKSTATION 4.3.), AW VolumeShare 5 (AW VOLUMESHARE 5 WITH ANGIOVIZ OPTION), AW Server. K052995: Advantage Workstation 4.3 is a review station, which allows easy selection, review, processing and filming of multi-modality DICOM images from a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0291-2014·2013-11-20
Beckman Coulter Recalls Access 2 Immunoassay System Due to Fuse Defect
Beckman Coulter is recalling the Access 2 Immunoassay System because the fuses may have the wrong amperage.
Product
Access 2 Immunoassay System, Part Number: 81600N The Access Immunoassay System is an in vitro diagnostic device used for the quantitative, semi-quantitative or qualitative determination of various analyte concentrations found in human body fluids.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·13V578000·2013-11-20
Mirage Cargo Trailer Recall for Door Lock Jamming Risk
Mirage is recalling 2006-2013 cargo trailers with Fastec door locks that may jam, potentially trapping occupants inside.
Product
MIRAGE — MIRAGE CARGO TRAILERS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0203-2014·2013-11-20
Hospira Recalls Plum A+ Hyperbaric Infusion Pumps Due to Calibration Drift
Hospira is recalling 179 Plum A+ Hyperbaric Infusion Pumps because distal pressure sensor calibration drift may cause false alarms or occlusions.
Product
Plum A+ Hyperbaric Infusion Pump; List Number 11005; Labeled in part: PLUM A+ HYPERBARIC; Product Usage: The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0204-2014·2013-11-20
Infusion pumps are recalled for distal pressure sensor drift
Hospira recalled 10,669 Plum A+ infusion pumps after reports of distal pressure sensor calibration drift. The issue may cause false occlusion alarms or distal occlusions.
Product
Plum A+ Infusion Pump; List Number: 11971; Product Usage: The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·13V580000·2013-11-20
Fleetwood Recalls 2014 Recreational Vehicles Due to Seat Belt Latch Issues
Fleetwood is recalling 774 model year 2014 recreational vehicles because the seat belt latch plate may remain partially engaged, making the belt difficult to unlatch.
Product
FLEETWOOD — FLEETWOOD, AMERICAN COACH TIOGA MONTARA, AMERICAN EAGLE, PROVIDENCE, TERRA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·13E064000·2013-11-20
Seats Incorporated Recalls Front Seat Belt Buckle Assemblies
Seats Incorporated is recalling front seat belt buckle assemblies that may fail to release when the button is pressed, increasing injury risk in a crash.
Product
SEAT BELTS:FRONT:BUCKLE ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0207-2014·2013-11-20
Hospira Recalls Plum A+ Infusion Pumps Due to Pressure Sensor Calibration Drift
Hospira is recalling 182,970 Plum A+ Infusion Pumps because pressure sensor calibration drift may cause false alarms or missed occlusions.
Product
Plum A+ Infusion Pump; List Number: 12391; Product Usage: The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0290-2014·2013-11-20
Hospira Recalls Plum A+ Infusion Systems Due to Broken Sensor Pin Risk
Hospira Inc. is recalling Plum A+ Infusion Systems because the distal pressure sensor pin may break, potentially preventing the detection of line occlusions.
Product
The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+ Infusion System is designed to deliver parenteral, enteral, or epidural infusions…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0289-2014·2013-11-20
Hospira Recalls Plum A+3 Infusion Systems Due to Broken Sensor Pin Risk
Hospira is recalling 21,551 Plum A+3 Infusion Systems because a distal pressure sensor pin may break, potentially preventing the detection of line occlusions.
Product
The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+3 Infusion System is designed to deliver parenteral, enteral, or epidural…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0206-2014·2013-11-20
Hospira Recalls Plum A+3 Infusion Pumps Due to Pressure Sensor Drift
Hospira is recalling 214 Plum A+3 Infusion Pump Systems because distal pressure sensor calibration drift may cause false alarms or occlusions.
Product
Plum A+3 Infusion Pump System; List Number: 12348; Product Usage: The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·13V577000·2013-11-20
Blue Bird Recalls 2014 Vision and All American Buses for Seat Belt Defect
Blue Bird is recalling 146 model year 2014 Vision and All American non-school buses because the driver's seat belt latch plate can become stuck, hindering egress.
Product
BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0286-2014·2013-11-20
Hospira Recalls Plum A+3 Infusion Systems Due to Broken Pressure Sensor Pin
Hospira is recalling 214 Plum A+3 Infusion Systems because a pressure sensor pin may break, potentially preventing the detection of line occlusions.
Product
The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+3 Infusion System is designed to deliver parenteral, enteral, or epidural…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0164-2014·2013-11-20
Apotheca Energique Gastrozyme Recalled for Potential Chloramphenicol Contamination
Grato Inc. is recalling Apotheca Energique Gastrozyme dietary supplements because they may contain chloramphenicol. The product was sold nationwide through retail and internet channels.
Product
Apotheca Energique Gastrozyme, dietary supplement, 100 vegetarian capsules.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0208-2014·2013-11-20
Hospira Recalls Plum A+ Infusion Pumps Due to Pressure Sensor Drift
Hospira is recalling 7,691 Plum A+ Infusion Pumps because pressure sensor calibration drift may cause false alarms or undetected occlusions.
Product
Plum A+ Infusion Pump; List Number: 12618; Product Usage: The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0279-2014·2013-11-20
Medtronic Activa Neurostimulators Recalled for Loss of Stimulation
Medtronic is recalling specific Activa rechargeable neurostimulators because they may lose stimulation when switching programs. Therapy can be restored using the Physician Recharge mode.
Product
Medtronic Activa PC, model 37601, and Activa RC, model 37612, Activa SC, models 37602 and 37603. Multi-program Rechargeable Neurostimulator for Deep Brain Stimulation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0285-2014·2013-11-20
Hospira Recalls Plum A+ Infusion Systems Due to Broken Sensor Pin Risk
Hospira is recalling 71 Plum A+ Infusion Systems because a pressure sensor pin may break, potentially preventing the detection of line occlusions.
Product
The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+ Infusion System is designed to deliver parenteral, enteral, or epidural infusions…
Category
Medical Device
Distribution
Distributed nationwide