State

US Virgin Islands product recalls

73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30626–30650 of 73896

LowFDA (Devices)·Z-0771-2020·2020-01-08
Nidek Specular Microscope Recalled for Electromagnetic Noise Exceeding Standards
Nidek, Inc. is recalling 13 Specular Microscopes, Model CEM-530, because their electromagnetic noise exceeded the upper limit of the Electromagnetic Compatibility Standard.
Product
NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact, high magnification image capture of endothelium enabling observation of the size and shape of cells. Information such as the number of endothelial cells, cell density, and cell area is…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0635-2020·2020-01-08
Lupin Recalls Bimatoprost Ophthalmic Solution Due to Impurity Specifications
Lupin Pharmaceuticals is recalling 2,130 bottles of Bimatoprost Ophthalmic Solution because an out-of-specification impurity was detected.
Product
Bimatoprost Ophthalmic Solution, 0.03%, For Use in the Eyes Only, Sterile, Rx Only, 7.5 mL bottle, Manufactured by: Lupin Limited, Pithampur (M.P.), INDIA, NDC: 68180-429-03.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·20V005000·2020-01-06
Micro Bird Recalls 2015-2019 T-Series Buses for Fire Risk
Micro Bird is recalling 2015-2019 T-Series school buses because an oversized circuit breaker may cause wire overheating and fire.
Product
MICRO BIRD — MICRO BIRD T-SERIES TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V004000·2020-01-06
Micro Bird Recalls CT-Series Shuttle Buses Due to Fire Risk
Micro Bird is recalling 2015-2019 CT-Series shuttle buses because an oversized breaker may cause wire overheating and fire. Owners should contact the manufacturer for a free replacement.
Product
MICRO BIRD — MICRO BIRD CT-SERIES
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·20V001000·2020-01-02
Subaru and Saab Vehicles Recalled for Air Bag Inflator Defect
Subaru is recalling specific 2003-2014 models and Saab 9-2X vehicles because passenger air bag inflators may explode due to humidity, posing a risk of serious injury or death.
Product
SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20E001000·2020-01-02
Takata Frontal Air Bag Inflators Recalled for Explosion Risk
Takata is recalling specific non-desiccated frontal air bag inflators used as interim remedies. These inflators may explode due to propellant degradation, posing a risk of serious injury or death.
Product
AIR BAGS:FRONTAL recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V003000·2020-01-02
Subaru and Saab Recall Vehicles Due to Air Bag Inflator Defect
Subaru is recalling specific 2003-2014 models and Saab 9-2X vehicles because passenger air bag inflators may explode, posing a risk of serious injury or death.
Product
SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V002000·2020-01-02
Subaru and Saab Recall Vehicles Due to Air Bag Inflator Defect
Subaru and Saab are recalling specific model years because passenger air bag inflators may explode due to humidity, posing a risk of serious injury.
Product
SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-01022020·2020-01-02
USDA Alerts on Sun Foods Egg Products Linked to Listeria Outbreak
USDA issued a public health alert for Sun Foods egg products containing ingredients from an FDA recall due to possible Listeria monocytogenes contamination.
Product
Sun Foods — FSIS Issues Public Health Alert for Products Associated with the FDA Almark Foods Recall Due to Possible Listeria Monocytogenes Contamination
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0744-2020·2020-01-01
Axis-Shield Homocysteine Reagent Recalled for Potential Performance Issues
Axis-Shield Diagnostics is recalling 740 units of Liquid Stable 2-Part Homocysteine Reagent due to potential performance issues detected during routine testing.
Product
Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHRWR1000 - Product Usage: The device can assist in the diagnosis and treatment of patients suspected of having hyperhomocysteinemia and homocystinuria. The device is intended for Professional use only.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0724-2020·2020-01-01
Bard Max-Core Biopsy Instrument Recalled for Firing Failures
Bard Peripheral Vascular Inc is recalling 727,034 units of the Bard Max-Core Disposable Core Biopsy Instrument due to complaints of failure to fire and failure to obtain samples.
Product
BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The core needle biopsy device is intended for use in obtaining biopsies from soft tissues such as liver, kidney, prostate, spleen, lymph nodes and various soft tissue tumors. It is not intended for use in bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0736-2020·2020-01-01
RayStation Radiation Therapy Software Recalled for Beam Editing Bug
RaySearch Laboratories is recalling RayStation software versions 4.0 through 9.0 because a bug may reset beam settings, requiring dose recalculation.
Product
RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0 - Product Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0719-2020·2020-01-01
3M Recalls Durapore Advanced Surgical Tape Due to Bond Failure Risk
3M is recalling Durapore Advanced Surgical Tape because long-term exposure to high moisture may cause bond failure and fiber fraying, posing a risk of accidental ingestion or aspiration.
Product
3M Durapore Advanced, Surgical Tape, Model Numbers: 1590-0, 1590-1, 1590-2, 1590-3, 1591-0, 1591-1, 1591-2, 1591-3, 1590S-1, 1590S-2, 1590B-118, 1590B-136
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0728-2020·2020-01-01
Cardinal Health Recalls S.M.A.R.T. Stents for Incorrect MRI Labeling
Cardinal Health is correcting labeling on S.M.A.R.T. Nitinol Stent Systems that incorrectly stated they were 'MRI Safe' instead of 'MRI Conditional'.
Product
S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent System. The SMART stent system includes a self-expanding stent made of Nitinol (nickel-titanium alloy) material and a 6 French (2.0 mm) or 7 French (2.3 mm) sheathed delivery system. The stent is laser…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0743-2020·2020-01-01
Axis-Shield Homocysteine Reagent Recalled for Potential Performance Issues
Axis-Shield Diagnostics is recalling 740 units of Liquid Stable 2-Part Homocysteine Reagent due to potential performance issues detected during routine testing.
Product
Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHRWR100 - Product Usage: The device can assist in the diagnosis and treatment of patients suspected of having hyperhomocysteinemia and homocystinuria. The device is intended for Professional use only.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0740-2020·2020-01-01
Ortho Clinical Diagnostics Recalls Urine Electrolyte Diluent Due to Instability
Ortho Clinical Diagnostics is recalling Urine Electrolyte Diluent because the product may become unstable when stored in a 2mL cup for 7 days.
Product
Urine Electrolyte Diluent, Product Code: 1112352 - Product Usage: used to dilute urine specimens for analysis of sodium (Na+) and potassium (K+) on VITROS 250/350/5,1 FS/4600 Chemistry Systems and the VITROS 5600/XT 7600 Integrated Systems.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0729-2020·2020-01-01
Cordis Precise Nitinol Stent System Labeling Correction for MRI Information
Cardinal Health is correcting labeling on Cordis Precise Nitinol Stent Systems because the instructions incorrectly stated the device was MRI Safe instead of MRI Conditional.
Product
Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent System devices are designed to deliver a flexible, self-expanding endoluminal stent to the carotid vasculature via over-the-wire (OTW) 5.5F or 6F sheathed delivery systems. The stent is cut from a solid…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0628-2020·2020-01-01
Spectrum Laboratory Products Recalls Subpotent Estriol Micronized USP
Spectrum Laboratory Products is recalling specific lots of Estriol Micronized USP because assay results did not meet specifications.
Product
Estriol [(16a, 17B)-Estra-1,3,5(10)-triene-3,16,17-triol; Oestriol] Micronized, USP, CAS 50-27-1, packaged in a) 1 G glass bottles, b) 5 G glass bottles, c) 25 G glass bottles, d) 100 G glass bottles, e) 500 G glass bottles, and f) 1 KG plastic bottles, Rx Only, Spectrum…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0730-2020·2020-01-01
Cardinal Health Recalls S.M.A.R.T. Stents for Incorrect MRI Labeling
Cardinal Health is correcting labeling on S.M.A.R.T. stents that incorrectly stated they were MRI Safe. The correct classification is MRI Conditional.
Product
Cordis S.M.A.R.T. CONTROL /S.M.A.R.T. Vascular Stent System. The S.M.A.R.T. CONTROL and S.M.A.R.T. Vascular Stent Systems consist of a self-expanding stent made of Nitinol (nickel-titanium alloy) material that is pre-mounted on an over-the-wire delivery system. The stents…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0723-2020·2020-01-01
Lifelines Neuro Recalls ElectroTek Temporal Sensor Cables for Labeling Errors
Lifelines Neuro is recalling 12 ElectroTek Temporal Sensor Cables due to potential incorrect placement labels that could lead to improper electrode placement during EEG studies.
Product
ElectroTek Temporal Sensor Cable Gold - Long Length, Single Length - Product Usage: The electroencephalographic system ElectroTek is intended to acquire, display, and store the electrical activity of a patient s brain obtained by placing electrodes on the patient s scalp. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0722-2020·2020-01-01
Lifelines Neuro Recalls ElectroTek EEG Sensor Cables Due to Labeling Error
Lifelines Neuro is recalling eight ElectroTek EEG temporal sensor cables because incorrect placement labels could lead to improper electrode positioning during brain activity studies.
Product
ElectroTek Temporal Sensor Cable Gold - Long Length, Graduated - Product Usage: The electroencephalographic system ElectroTek is intended to acquire, display, and store the electrical activity of a patient s brain obtained by placing electrodes on the patient s scalp. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0720-2020·2020-01-01
Abbott Recalls Mislabeled Radiofrequency Cannulas Due to Manufacturing Error
Abbott Medical is recalling 470 radiofrequency cannulas that were incorrectly labeled with a 5mm active tip length instead of 10mm.
Product
CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compatible Electrode, REF C-1005-S - Product Usage: Disposable Radiofrequency Cannulae are provided in either straight, curved, or curved blunt geometries with a stylet inserted in the cannula. Cannulae are insulated except for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0739-2020·2020-01-01
Ortho Clinical Diagnostics Recalls VITROS 7% BSA Diluent Due to Instability
Ortho Clinical Diagnostics is recalling VITROS 7% BSA diluent because it may become unstable when stored in a 2mL cup for seven days.
Product
7% BSA (Bovine Serum Albumin), Product Code: 8262487 - Product Usage: is used to dilute samples when assay values exceed the reportable (dynamic) range using the VITROS 250/350/5,1 FS/4600 Chemistry Systems and VITROS 5600/XT 7600 Integrated Systems.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0742-2020·2020-01-01
Axis-Shield Homocysteine Reagent Recalled for Potential Performance Issues
Axis-Shield Diagnostics is recalling 740 units of Liquid Stable 2-Part Homocysteine Reagent due to potential under-recovery of sample results.
Product
Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHBC100 - Product Usage: The device can assist in the diagnosis and treatment of patients suspected of having hyperhomocysteinemia and homocystinuria. The device is intended for Professional use only.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0626-2020·2020-01-01
Pharmedium Recalls Subpotent Repinephrine Bitartrate Injection Bags Nationwide
Pharmedium Services LLC is voluntarily recalling 864 bags of repinephrine bitartrate injection because the drug was subpotent. The recall covers nationwide distribution in the U.S.
Product
NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 508.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.
Category
Drug
Distribution
Distributed nationwide