State

US Virgin Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46401–46425 of 73987

HighFDA (Devices)·Z-0038-2017·2016-10-12
RayStation Radiation Therapy Planning Software Recalled for Dose Calculation Errors
RaySearch is recalling RayStation software versions 2.5 through 5.0 due to dose calculation errors when using specific region of interest settings.
Product
RayStation 2.5, 3.0, 3.5, 4.0, 4.5, 4.7, 5.0 and 4.3 (InverseArc 1.0) -- Radiation Therapy Treatment Planning System RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2905-2016·2016-10-12
Integra Straight Ventricular Catheter Recalled for Incomplete Packaging Seal
Integra LifeSciences Corp. is recalling 10 units of Straight Ventricular Catheters due to an incomplete packaging seal discovered during final inspection.
Product
Integra Straight Ventricular Catheter F8, 25 cm, Sterile EO, Rx only, packaged in a Tyvek pouch and secondary packaged in to Tyvek pouch, sealed in a cardboard box. Silicone elastomer Ventricular Catheter for use with hydrocephalus valves
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2909-2016·2016-10-12
Integra Ventricular Catheter Accessory Kit Recalled for Incomplete Packaging Seal
Integra LifeSciences Corp. is recalling 14 units of the Ventricular Catheter Accessory Kit due to an incomplete sterile packaging seal discovered during final inspection.
Product
Integra Ventricular Catheter Accessory Kit, REF 951303, Sterile EO, Rx only, packaged in a PVC tray, then secondary package in to Tyvek pouch and tertiary packaged in to Tyvek pouch. Sealed pouches are packaged in a cardboard box. F8 35cm Silicone Elastomer Ventricular…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0039-2017·2016-10-12
Siemens Dimension Vista Calcium Reagent Cartridge Recall for Erroneous Results
Siemens Healthcare Diagnostics is recalling Dimension Vista Calcium reagent cartridges that may produce inaccurate test results.
Product
Dimension Vista¿ Calcium (CA) Flex¿ reagent cartridge Device Listing No.: D011443 Batch Number: 16060BB
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0014-2017·2016-10-12
Siemens Recalls Multix Fusion VA10 Radiographic Systems Due to Table Defect
Siemens is recalling 37 Multix Fusion VA10 radiographic systems because a table part may detach, causing the table to tilt and potentially injure patients.
Product
Multix Fusion VA10 Product Usage: The Multix Fusion VA10 system is a radiographic system used in hospitals, clinics, and medical practices. Multix Fusion enables radiographic exposures of the whole body including:skull, chest, abdomen and extremities and may be used on…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0008-2017·2016-10-12
Microgenics Recalls QMS Everolimus Assay Due to Reagent Stability Issue
Microgenics Corporation is recalling the Thermo Scientific QMS Everolimus Assay because a reagent stability issue causes inaccurate test results for transplant patients.
Product
Thermo Scientific QMS Everolimus Assay; Model number: 0380000 (US Distribution); 0373852 (Foreign Distribution) Product Usage: The QMS Everolimus Assay is intended for the quantitative determination of Everolimus, in human whole blood on automated clinical chemistry…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·17010·2016-10-12
Mamas & Papas Recalls Armadillo Strollers Due to Fall Hazard
Mamas & Papas is recalling Armadillo Flip and Flip XT strollers because a loose latch can cause the seat to tip back, posing a fall hazard to infants.
Product
Mamas & Papas Armadillo Flip Strollers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·16V728000·2016-10-12
Forest River Recalls 2017 Trailers Due to Air Conditioner Fire Risk
Forest River is recalling 2017 Flagstaff and Rockwood trailers because excess slack in air conditioner wiring may contact heating elements, increasing fire risk.
Product
FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0016-2017·2016-10-12
Panoramic PC-1000 X-ray Systems Recalled for Safety Nut Defect
Panoramic Rental Corp. is voluntarily correcting PC-1000 X-ray systems because a safety nut may be ineffective, posing a risk of blunt force trauma to the head, neck, or shoulders.
Product
Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser1000 will enable the user to take panoramic x-ray images as well as cephalometric x-ray images.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V727000·2016-10-12
Keystone Recalls 2017 Dutchmen Coleman Trailers for Wiring Fire Risk
Keystone RV is recalling 84 model year 2017 Dutchmen Coleman recreational trailers because loose or frayed wiring in the power center may increase the risk of a fire.
Product
DUTCHMEN — DUTCHMEN COLEMAN
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0005-2017·2016-10-12
Teva Recalls Claravis Isotretinoin Capsules Due to Impurity Failures
Teva North America is recalling Claravis (isotretinoin) capsules because they failed impurity and degradation specifications.
Product
Claravis (isotretinoin capsules USP), 10mg, packaged in carton containing 3 Blister Packs of 10 Capsules Each (30 Capsules total); Rx only, TEVA PHARMACEUTICALS USA, Sellersville, PA 18960. NDC 00555-1054-86
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0024-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color A3.5 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 17 units of Zenostar MT Color A3.5 dental porcelain coloring liquid due to potential packaging leaks that may cause skin irritation.
Product
Zenostar MT Color A3.5 60ml, art. no. 681053. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2906-2016·2016-10-12
Integra CUSA Dissectron Fingertip Laparoscopic Cannula Recalled for Packaging Seal Defect
Integra LifeSciences is recalling 9 units of CUSA Dissectron Fingertip Laparoscopic Cannulas due to incomplete sterile packaging seals discovered during final inspection.
Product
CUSA Dissectron Fingertip Laparoscopic Cannula, REF F75221, Sterile EO, Rx only, packaged in a Tyvek pouch and secondary packaged in Tyvek pouch, Five (5) sealed pouches are packaged in a cardboard box. For use with CUSA DISSECTRON Hand pieces and Sontrodes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0008-2017·2016-10-12
West-Ward Recalls Prednisone Tablets Due to Underweight Specification Failure
West-Ward Pharmaceuticals is recalling 15,109 bottles of Prednisone 1 mg tablets because an underweight tablet was discovered.
Product
PREDNISONE — PREDNISONE (PREDNISONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0018-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color Impulse Brown Dental Porcelain
Ivoclar Vivadent is recalling 11 units of Zenostar MT Color Impulse brown dental porcelain due to potential packaging leaks that may cause skin irritation.
Product
Zenostar MT Color Impulse brown, art. no. 681169 Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0012-2017·2016-10-12
Philips Ingenuity CT Scanner Recalled for Infant Head Image Quality Issues
Philips Medical Systems is recalling 235 Ingenuity CT scanners because infant head scans in High Resolution mode may produce degraded image quality, including non-uniformity and CT number shifts.
Product
Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0017-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color Impulse Blue Dental Porcelain
Ivoclar Vivadent is recalling 79 units of Zenostar MT Color Impulse blue dental porcelain due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color Impulse blue, Art. no. 681165 Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0032-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color C3 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 13 units of Zenostar MT Color C3 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color C3 60ml, art. no. 681061. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0028-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color B3 Dental Porcelain Liquid
Ivoclar Vivadent is recalling 27 units of Zenostar MT Color B3 dental porcelain liquid due to potential packaging leaks that may cause skin irritation.
Product
Zenostar MT Color B3 60ml, art. no. 681057. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0027-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color B2 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 15 units of Zenostar MT Color B2 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color B2 60ml, art. no. 681056. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0026-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color B1 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 43 units of Zenostar MT Color B1 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color B1 60ml, art. no. 681055. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0035-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color D3 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 18 units of Zenostar MT Color D3 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color D3 60ml, art. no. 681064. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0036-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color D4 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 9 units of Zenostar MT Color D4 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color D4 60ml, art. no. 681065. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0033-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color C4 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 10 units of Zenostar MT Color C4 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color C4 60ml, art. no. 681062. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0023-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color A3 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 42 units of Zenostar MT Color A3 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color A3 60ml, art. no. 681052. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide