State

US Virgin Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35651–35675 of 73915

SevereFDA (Drugs)·D-0337-2019·2018-12-26
Tris Pharma Recalls Infants' Ibuprofen Due to Higher Concentration
Tris Pharma is recalling specific lots of Infants' Ibuprofen because they may contain a higher concentration of the active ingredient.
Product
Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye Free, Non-staining Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 39338 3.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0626-2019·2018-12-26
FDA Recalls Covidien Emprint Percutaneous Antenna Due to Tip Disengagement
FDA is recalling specific lots of the Covidien Emprint Short Percutaneous Antenna because the ceramic trocar tip may disengage from the needle shaft during use, potentially remaining in the patient.
Product
Covidien Emprint Short Percutaneous Antenna with Thermosphere Technology, Material CA15L2 intended for use in percutaneous, laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of nonresectable liver tumors.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0336-2019·2018-12-26
Tris Pharma Recalls Superpotent Infants' Ibuprofen Suspension
Tris Pharma is recalling 19,488 bottles of Infants' Ibuprofen due to potential higher-than-labeled ibuprofen concentrations.
Product
Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye-Free Non-Staining Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by Family Dollar Services, Inc., 10301 Monroe Road, Matthews, NC 28105, NDC 55319-250-23, UPC 0 32251 03374 2.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0335-2019·2018-12-26
Tris Pharma Recalls Infants' Ibuprofen Due to Higher Concentration
Tris Pharma is recalling specific lots of infants' ibuprofen oral suspension because they may contain a higher concentration of the active ingredient.
Product
infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg per 1.25 mL, Dye-Free Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by Wal-Mart Stores, Inc., Bentonville, AR 72716, NDC 49035-125-23, UPC 0 78742 02016 7.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0333-2019·2018-12-26
Pharmedium Recalls Sub-Potent Fentanyl and Ropivacaine Injection Syringes
Pharmedium Services, LLC is voluntarily recalling 295 syringes of a fentanyl and ropivacaine injection that were found to be sub-potent.
Product
Fentanyl Citrate 2 mcg per mL (100 mcg per 50 mL) and Ropivacaine HCl 0.1% in Sodium Chloride 0.9%, Injection, 50 mL total volume in a 60 mL BD Syringe, Rx Only, PharMEDium Services, LLC. 913 N. Davis Ave. Cleveland, MS 38732 NDC 61553-644-75.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0627-2019·2018-12-26
FDA Recalls Covidien Emprint Percutaneous Ablation Antenna Due to Tip Disengagement
FDA is recalling the Covidien Emprint Standard Percutaneous Antenna because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.
Product
Covidien Emprint Standard Percutaneous Antenna with Thermosphere Technology, CA20L2 intended for use in percutaneous, laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of nonresectable liver tumors.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0338-2019·2018-12-26
Gordon Laboratories Recalls Monsel's Solution Due to High Iron Levels
Gordon Laboratories is recalling specific batches of Monsel's (Ferric Subsulfate) Solution because they contain higher levels of iron than labeled.
Product
Monsel's (Ferric Subsulfate) Solution, 8 mL amber glass bottle, packaged as one dozen bottles with applicators per box, Rx only, Gordon Laboratories, Upper Darby, PA 19082, NDC 10481-0112-8.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0625-2019·2018-12-26
FDA Recalls Covidien Emprint Percutaneous Antenna Due to Tip Disengagement
FDA is recalling specific lots of the Covidien Emprint Long Percutaneous Antenna because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.
Product
Covidien Emprint Long Percutaneous Antenna with Thermosphere Technology, Material CA30L2 intended for use in percutaneous, laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of nonresectable liver tumors.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0339-2019·2018-12-26
Pfizer Recalls Levoxyl Levothyroxine Sodium Tablets Due to Superpotency
Pfizer is voluntarily recalling 1,996 bottles of Levoxyl 112 mcg tablets nationwide because the drug is superpotent.
Product
LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0334-2019·2018-12-26
Pharmedium Recalls Sub-Potent Fentanyl and Ropivacaine Injection Bags
Pharmedium Services, LLC is voluntarily recalling 295 bags of Fentanyl Citrate and Ropivacaine HCl injection because the product was found to be sub-potent.
Product
Fentanyl Citrate 2 mcg per mL (200 mcg per 100 mL) and Ropivacaine HCl 0.2% in Sodium Chloride 0.9%, Injection, 100 mL total volume in a 150 mL Intravia Bag, Rx Only,PharMEDium Services, LLC. 913 N. Davis Ave. Cleveland, MS 38732. NDC 61553-148-48
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0617-2019·2018-12-26
Siemens Dimension Vista 1500 Recalled for Potential Sample Contamination
Siemens is recalling Dimension Vista 1500 instruments due to a software issue that may cause sample contamination if tests are manually cancelled during aliquoting.
Product
Dimension Vista 1500, Model No. 10444801 an in vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluids.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0652-2019·2018-12-26
Ortho-Clinical Diagnostics Recalls VITROS 3600 Immunodiagnostic System Software
Ortho-Clinical Diagnostics is recalling VITROS 3600 Immunodiagnostic System units due to a software anomaly that may incorrectly extend reagent stability time.
Product
VITROS¿ 3600 Immunodiagnostic System, Version 3.3.1 & below For use in the in vitro quantitative measurement of a variety of analytes of clinical interest in certain biological fluids (depending on the analyte) such as serum, plasma, urine and cerebrospinal fluid.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0639-2019·2018-12-26
bioMerieux Recalls VITEK 2 Systems Software Version 9.01 Update Kit
bioMerieux is recalling VITEK 2 Systems Software Version 9.01 Update Kits because they may display incorrect organism identification and antimicrobial susceptibility testing results.
Product
VITEK¿ 2 Systems Software Version 9.01 Update Kit.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0645-2019·2018-12-26
Deerfield Imaging Recalls IMRIS T2X Tables Due to Roll Position Drift
Deerfield Imaging is recalling 15 IMRIS T2X tables because they may drift in the roll position while in use.
Product
IMRIS T2X table, Part Numbers: (a)108000-000, (b)108000-600, (c)109682-000, (d) 109682-600, (e) 110470-600 - Product Usage: The ORT200 and ORT300 are intended for use during diagnostic examinations, radiologic procedures, or surgical procedures to support and position a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0648-2019·2018-12-26
Deerfield Imaging Recalls IMRIS ORT 300 Operating Room Tables
Deerfield Imaging is recalling 14 IMRIS ORT 300 operating room tables because they may drift in the roll position while in use.
Product
IMRIS ORT 300, Removable Operating Room Table, Part Numbers: (a) 114093-000, (b) 114093-006 - Product Usage: The ORT200 and ORT300 are intended for use during diagnostic examinations, radiologic procedures, or surgical procedures to support and position a patient. The tables…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0659-2019·2018-12-26
Konica Minolta Recalls 151 X-Ray Systems Due to Unintentional Movement
Konica Minolta is recalling 151 Advanced Universal U-Arm 4000 X-ray systems because the U-Arm may move unintentionally.
Product
Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17; Board Name; Board Version, Firmware Version Advanced Universal U-Arm 4000 System. The Positioner consists of the following associated subassemblies: Vertical Column, Swivel Arm with variable height, X-ray…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V932000·2018-12-26
Spartan Metrostar and Gladiator Fire Apparatus Brake Recall
Spartan is recalling 2011-2019 Metrostar and Gladiator fire apparatus vehicles due to a brake release delay that may hinder movement and increase crash risk.
Product
SPARTAN — SPARTAN METROSTAR, GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0649-2019·2018-12-26
Foundation Medicine Recalls 800 FoundationOne CDx Test Reports
Foundation Medicine is recalling 800 FoundationOne CDx test reports because an incorrect result for a single analyte may have been reported.
Product
FoundationOne CDx Test Results
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0647-2019·2018-12-26
Deerfield Imaging Recalls IMRIS ORT 200 Tables Due to Roll Drift
Deerfield Imaging is recalling 14 IMRIS ORT 200 operating room tables because they may drift in the roll position while in use.
Product
IMRIS ORT 200, Removable Operating Room Table, Part Numbers: (a) 113821-000, (b) 113821-600, (c) 114148-000, (d) 114148-600 - Product Usage: The ORT200 and ORT300 are intended for use during diagnostic examinations, radiologic procedures, or surgical procedures to support and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0646-2019·2018-12-26
Deerfield Imaging Recalls IMRIS ORT 100 Tables Due to Roll Drift
Deerfield Imaging is recalling 27 IMRIS ORT 100 tables because they may drift in the roll position during use, posing a risk of patient injury.
Product
IMRIS ORT 100 table, Part Numbers: (a) 110470-000, (b) 110470-600 - Product Usage: The ORT200 and ORT300 are intended for use during diagnostic examinations, radiologic procedures, or surgical procedures to support and position a patient. The tables are indicated for imagining…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0618-2019·2018-12-26
bioMerieux Recalls VITEK 2 Streptococcus Susceptibility Cards Due to False Results
bioMerieux is recalling VITEK 2 Streptococcus Susceptibility Cards because they may produce false resistant results for specific Streptococcus strains.
Product
VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more of these susceptibility products: Catalog # 410028, VITEK 2 AST-ST01 Catalog # 420915, VITEK 2 AST-ST02 Catalog # 421040, VITEK 2 AST-ST03 The VITEK 2 Streptococcus Susceptibility Card is intended for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0643-2019·2018-12-26
Theragenics Brachytherapy Applicator Needles Recalled for Unsealed Pouches
Theragenics is recalling Brachytherapy Applicator Needles because some pouches were not sealed, potentially compromising sterility.
Product
Theragenics Applicator Needle (18g x 20cm) The device is comprised four basic elements; a wire stylus with plastic handle, a plastic needle hub, a protective needle sleeve and the hollow steel needle.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0650-2019·2018-12-26
Ortho-Clinical VITROS 5600 Recall for Software Stability Anomaly
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems due to a software anomaly that may incorrectly extend reagent stability time.
Product
VITROS 5600 Integrated System, Version 3.3.1 & below For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Product Slides, VITROS Chemistry Products MicroTip Reagents and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0616-2019·2018-12-26
Siemens Dimension Vista 500 Recalled for Sample Contamination Risk
Siemens is recalling Dimension Vista 500 instruments due to a software issue that may cause sample contamination if tests are manually cancelled during aliquoting.
Product
Dimension Vista 500, model no. 10284473 an in vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluids.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0654-2019·2018-12-26
Bracco Recalls Empower FastLoad CT Syringe Packs Due to Seal Defect
Bracco is recalling 33,350 Empower FastLoad CT Syringe Packs because an insufficient seal on the sterile barrier may compromise the device's sterility.
Product
Empower FastLoad CT Syringe Pack -sterile disposable syringe kit for use with the EmpowerCT¿, EmpowerCTA¿ and EmpowerCTA¿+ Injector Systems SKU 017344/6720 Empower FastLoad" CT Syringe Pack is a sterile, disposable syringe kit designed for use with EmpowerCT¿, EmpowerCTA¿…
Category
Medical Device
Distribution
Distributed nationwide