State

US Virgin Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38151–38175 of 73916

HighFDA (Devices)·Z-1884-2018·2018-06-13
Santajoy Laser Projectors Recalled for Exceeding Federal Radiation Standards
Santajoy Ornament & Giftware Co. is recalling E-Z Illuminations laser projectors because they may emit radiation exceeding federal standards for Class IIIa products.
Product
Santajoy Ornament & Giftware Co., Ltd E-Z Illuminations Northern Lights E-Z Illuminations Galaxy Laser projectors that emit various colors and light patterns for entertainment and decorative purposes.
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2076-2018·2018-06-13
Tosoh ST-AIA PACK IRI Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK IRI assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK IRI; Part Number: 025260 Assay, Diabetes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2066-2018·2018-06-13
Tosoh ST-AIA PACK CEA Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK CEA assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK CEA; Part Number: 025254 Assay, Tumor Marker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2081-2018·2018-06-13
Tosoh Thyroid Assay Recalled Due to Strensiq Interference
Tosoh Bioscience is recalling ST-AIA PACK FT4 assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK FT4; Part Number: 025268 Assay, Thyroid
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2055-2018·2018-06-13
Becton Dickinson Recalls BD Vacutainer Plus SST Tubes Due to Stopper Defect
Becton Dickinson is recalling BD Vacutainer Plus SST tubes because the stoppers may pull out of the tubes.
Product
BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold, Catalog No. 367983
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2086-2018·2018-06-13
Tosoh FSH Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc. is recalling ST-AIA PACK FSH assays because the drug Asfotase Alfa (Strensiq) can cause inaccurate test results.
Product
ST-AIA PACK FSH; Part Number: 025265 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2078-2018·2018-06-13
Tosoh Thyroid Assay Recalled Due to Drug Interference
Tosoh Bioscience is recalling ST-AIA PACK TT3 thyroid assays because the drug Strensiq interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK TT3; Part Number: 025282 Assay, Thyroid
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2056-2018·2018-06-13
BD Vacutainer Plus SST Tubes Recalled for Stopper Defect
Becton Dickinson is recalling BD Vacutainer Plus SST tubes because the stoppers may pull out of the tube.
Product
BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold, Catalog No. 367986
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0841-2018·2018-06-13
Apotex Recalls Fluticasone Propionate Nasal Spray Due to Glass Particles
Apotex Inc. is recalling Fluticasone Propionate Nasal Spray because glass particles were found in the product. Consumers should stop using the affected lot.
Product
FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2089-2018·2018-06-13
Tosoh ST-AIA PACK hsE2 Recalled Due to Strensiq Interference
Tosoh Bioscience is recalling ST-AIA PACK hsE2 assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK hsE2; Part Number: 025225 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2065-2018·2018-06-13
Tosoh ST-AIA PACK AFP Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK AFP assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK AFP; Part Number: 025252 Assay, Tumor Marker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2088-2018·2018-06-13
Tosoh Estradiol Assay Recalled Due to Strensiq Interference
Tosoh Bioscience is recalling ST-AIA PACK Estradiol assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK Estradiol; Part Number: 025274 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2069-2018·2018-06-13
Tosoh ST-AIA CA 19-9 Assay Recalled Due to Drug Interference
Tosoh Bioscience is recalling ST-AIA PACK CA 19-9 assays because the drug Strensiq interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK CA 19-9; Part Number: 025271 Assay, Tumor Marker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2095-2018·2018-06-13
Tosoh ST-AIA PACK HGH Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK HGH assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK HGH; Part Number: 025266 Assay, Metabolic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2090-2018·2018-06-13
Tosoh ST-AIA PACK LH II Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK LH II assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK LH II; Part Number: 025296 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2093-2018·2018-06-13
Tosoh ST-AIA PACK Testosterone Assay Recalled Due to Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK Testosterone assays because Asfotase Alfa interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK Testosterone; Part Number: 025204 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2075-2018·2018-06-13
Tosoh ST-AIA C-Peptide II Assay Recalled Due to Drug Interference
Tosoh Bioscience is recalling ST-AIA PACK C-Peptide II assays because the drug Asfotase Alfa can cause inaccurate test results.
Product
ST-AIA PACK C-Peptide II; Part Number: 025283 Assay, Diabetes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1545-2018·2018-06-13
Dean Foods Recalls Baskin Robbins Mint Chocolate Chip Ice Cream
Dean Foods is recalling Baskin Robbins Mint Chocolate Chip ice cream because it may contain unlabeled coconut, a major food allergen.
Product
Baskin Robbins Mint Chocolate Chip
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2073-2018·2018-06-13
Tosoh ST-AIA PACK cTnI 2nd Gen Recalled Due to Drug Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK cTnI 2nd Gen assays because the drug Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK cTnI 2nd Gen; Part Number: 025205 Assay, Cardiac Marker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2101-2018·2018-06-13
GE Healthcare Recalls Centricity PACS-IW Medical Image Viewer
GE Healthcare is recalling 44 units of the Centricity PACS-IW with Universal Viewer because image series may be missing without warning.
Product
Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device that displays medical images (including mammograms) and data from various imaging sources. Images and data can be viewed, communicated, processed and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2087-2018·2018-06-13
Tosoh Prolactin Assay Recalled Due to Strensiq Interference
Tosoh Bioscience is recalling ST-AIA PACK Prolactin assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK Prolactin; Part Number: 025255 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2099-2018·2018-06-13
Tosoh ST-AIA PACK Cystatin C Assay Recalled Due to Drug Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK Cystatin C assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK Cystatin C; Part Number: 025217 Assay, Kidney Marker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2094-2018·2018-06-13
Tosoh ST-AIA PACK Cort Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK Cort assays because the drug Strensiq interferes with the tests, potentially causing inaccurate results.
Product
ST-AIA PACK Cort; Part Number: 025287 Assay, Metabolic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2103-2018·2018-06-13
NordicNeuroLab fMRI AudioSystem Recalled for Acoustic Distortion and Heat
NordicNeuroLab AS is recalling 64 fMRI AudioSystem units after a patient reported acoustic distortion and heat from headphones during a scan.
Product
fMRI Hardware System - AudioSystem, Version 1.0 The AudioSystem allows auditory signals from the stimulus presentation PC to enter the scanner room and to be presented to the patient. A communication console allows the operator to adjust the sounds from the PC and to speak to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2084-2018·2018-06-13
Tosoh ST-AIA PACK HCG Assay Recalled Due to Strensiq Interference
Tosoh Bioscience Inc is recalling ST-AIA PACK HCG assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Product
ST-AIA PACK HCG; Part Number: 025256 Assay, Reproductive Hormone
Category
Medical Device
Distribution
Distributed nationwide