State

US Virgin Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32676–32700 of 73900

HighFDA (Devices)·Z-2153-2019·2019-08-14
SenTec Standard Starter Set Recalled for Potential Electrolyte Deficiency
SenTec AG is recalling Standard Starter Sets due to a risk of missing or reduced electrolyte application during the membrane change procedure.
Product
SenTec Standard Starter Set with and without Service Gas (2 changers each) - Product Usage: Is indicated for continuous, non-invasive monitoring of carbon dioxide tension and oxygen tension as well as oxygen saturation and pulse rate in adult and pediatric patients. In neonatal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1659-2019·2019-08-14
RXQ Compounding Recalls Fentanyl and Bupivacaine Syringes Due to Sterility Concerns
RXQ Compounding LLC is recalling Fentanyl and Bupivacaine syringes nationwide due to a lack of assurance of sterility.
Product
FENTANYL 2MCG/ML BUPIVACAINE 0.125% IN NACL 0.9% SRY C-II, 50ML per syringe (C-II) RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0207-89
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1665-2019·2019-08-14
RXQ Compounding Recalls Hydromorphone Syringes Due to Sterility Concerns
RXQ Compounding LLC is recalling hydromorphone syringes because the company cannot ensure the product is sterile.
Product
HYDROMORPHONE 0.2MG/ML IN NACL 0.9% SYR (C-II) , [a) 50 ML NDC 70731-0114-89; b) 55 ML NDC 70731-0114-95] per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2209-2019·2019-08-14
Bard EnCor Breast Biopsy Probes Recalled for Leaks and Suction Issues
Bard Peripheral Vascular Inc is recalling EnCor Breast Biopsy Probes due to increased complaints about leaks, suction issues, and failure to obtain samples.
Product
EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF number 10G - REF ECP0110G. Product Usage: Indicated for use in acquiring tissue for diagnosing breast abnormalities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2148-2019·2019-08-14
Olympus MAJ-209 Single Use Suction Valves Recalled for Potential Malfunction
Olympus is recalling MAJ-209 Single Use Suction Valves because they may come apart or remain stuck inside endoscopes.
Product
Olympus MAJ-209 Single Use Suction Valves, Model Number MAJ-209 Product Usage: This product has been designed to be attached to the suction cylinder of compatible endoscopes for aspirating fluid from the distal end of the endoscopes through the instrument channel. Compatible…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2151-2019·2019-08-14
Fresenius Recalls Liberty Cycler Cassettes Due to Potential Solution Leakage
Fresenius Medical Care is recalling Liberty Cycler Cassettes because damaged units may leak dialysis solution into the cycler, posing a contamination risk.
Product
Liberty Cycler Cassettes (a disposable cassette that is intended to be used to perform peritoneal dialysis (APD) in conjunction with the Liberty cycler as follows: (1) LIBERTY Line Cycler Set with Stay-safe connectors (Dual Patient Connector) Part Number: 050-87212 (2)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2165-2019·2019-08-14
Centurion Neonatal PICC Insertion Tray Recalled for Packaging Compromise
Centurion Medical Products is recalling 120 Neonatal PICC Insertion Trays because the sterile packaging may be compromised, posing a risk of infection.
Product
NEONATAL PICC INSERTION TRAY Kit Code: CVI2310 - Product Usage: Kit is used for Peripheral Central Line Insertion procedures on newborns.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1664-2019·2019-08-14
RXQ Compounding Recalls Hydrogen Peroxide Injectable Due to Sterility Concerns
RXQ Compounding LLC is recalling Hydrogen Peroxide 3% Injectable PFV because the product lacks assurance of sterility. The recall covers all lots within expiry distributed nationwide.
Product
HYDROGEN PEROXIDE 3% INJECTABLE PFV, 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0907-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2138-2019·2019-08-14
MED-EL PULSARci100 Cochlear Implant Recalled for Leak Test Failures
MED-EL is recalling PULSARci100 Cochlear Implants because they failed helium-fine leak tests. Affected devices were distributed in the US and several international countries.
Product
MED EL Cochlear Implant System, PULSARci100 Standard - Product Usage: The PULSARci100 Implant is an implantable part of the MED EL Cochlear Implant System and can only be used together with compatible MED EL external components. The MED EL Cochlear Implant System is intended to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2210-2019·2019-08-14
Bard EnCor Breast Biopsy Probes Recalled for Leaks and Suction Issues
Bard Peripheral Vascular Inc is recalling EnCor Breast Biopsy Probes due to increased complaints of leaks, suction issues, and failure to obtain tissue samples.
Product
EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF numbers 10GV Upright (Vertical) - REF ECP0110GV. Product Usage: Indicated for use in acquiring tissue for diagnosing breast abnormalities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1636-2019·2019-08-14
RXQ Compounding Recalls Ascorbic Acid Injection Due to Crystallization
RXQ Compounding LLC is voluntarily recalling Ascorbic Acid 500 MG/ML Injection due to crystallization. The recall covers all lots within expiry distributed nationwide.
Product
Ascorbic Acid 500 MG/ML (Non-Corn) INJ (MDV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0975-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2180-2019·2019-08-14
Ortho VITROS 5600 Analyzer Recalled for Software Calibration Anomaly
Ortho Clinical Diagnostics is recalling 89 VITROS 5600 clinical chemistry analyzers worldwide due to a software anomaly that may cause unsuccessful calibrations.
Product
VITROS 5600 Integrated System, clinical chemistry analyzer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2187-2019·2019-08-14
Philips CT System Recall for Incorrect Cardiac Image Labeling
Philips is recalling 116 CT systems because cardiac images may be incorrectly labeled as having phase tolerance applied when it was not.
Product
Ingenuity Core128 Model # 728323, computed tomography x-ray system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1611-2019·2019-08-14
Herbal Doctor Remedies Recalls Pain Away Capsules for Manufacturing Deviations
Herbal Doctor Remedies is recalling Pain Away 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices.
Product
Pain Away, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1605-2019·2019-08-14
Herbal Doctor Remedies Recalls Lube Lax Capsules for Manufacturing Violations
Herbal Doctor Remedies is recalling Lube Lax Capsules because they were manufactured outside of current Good Manufacturing Practices controls.
Product
Lube Lax Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1614-2019·2019-08-14
Herbal Doctor Remedies Recalls Psoriasis Balm Due to Manufacturing Deviations
Herbal Doctor Remedies is recalling Psoriasis Balm because it was manufactured outside of current Good Manufacturing Practice controls.
Product
Psoriasis Balm, 60 gram, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1597-2019·2019-08-14
Herbal Doctor Remedies Recalls Fungo Balm Due to Manufacturing Deviations
Herbal Doctor Remedies is recalling Fungo Balm because it was manufactured outside of required Good Manufacturing Practices controls.
Product
Fungo Balm, 30 gram, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1594-2019·2019-08-14
Dragon Pain Balm Recalled for CGMP Manufacturing Deviations
Herbal Doctor Remedies is recalling Dragon Pain Balm because it was manufactured outside of current Good Manufacturing Practices controls.
Product
Dragon Pain Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1632-2019·2019-08-14
Unipharma Recalls DrKids Children's Allergy Relief Diphenhydramine Due to B. cepacia Risk
Unipharma is recalling DrKids Children's Allergy Relief Diphenhydramine vials due to a precautionary measure regarding potential contamination with B. cepacia bacteria.
Product
DrKids Children's Allergy Relief Diphenhydramine HCl 12.5 mg/5 mL Antihistamine, Mixed berry Flavor, 20 Pre-measured Single-Use vials per Carton, Manufactured in USA by: Unipharma, LLC. Tamarac, FL 33321, UPC 370302255010
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2143-2019·2019-08-14
Biomet 3i Recalls Certain Bellatek Tin Abutments Due to Manufacturing Defect
Biomet 3i is recalling 2 units of Bellatek Tin Abutments because a manufacturing defect causes the screw head to seat too deep without a positive stop.
Product
CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM, Item Number ILDAN3 - Product Usage: BIOMET3i Restorative products are intended for use as an accessory to endosseous dental implants for placement in the maxilla and mandible
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1623-2019·2019-08-14
Herbal Doctor Remedies Recalls Smoke End Capsules for Manufacturing Violations
Herbal Doctor Remedies is recalling Smoke End Capsules because they were manufactured outside of current Good Manufacturing Practices controls.
Product
Smoke End Capsules,Distributed Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1615-2019·2019-08-14
Herbal Doctor Remedies Recalls Sperm Booster for Manufacturing Violations
Herbal Doctor Remedies is recalling Sperm Booster because it was manufactured outside of required Good Manufacturing Practice controls.
Product
Sperm Booster, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1600-2019·2019-08-14
Herbal Doctor Remedies Recalls Herpes-G Capsules for Manufacturing Violations
Herbal Doctor Remedies is recalling Herpes-G Capsules because they were manufactured outside of current Good Manufacturing Practices (CGMP) controls.
Product
Herpes-G Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2175-2019·2019-08-14
Ortho VITROS 250 Chemistry System Recalled for Software Calibration Anomaly
Ortho Clinical Diagnostics is recalling two VITROS 250 Chemistry Systems due to a software anomaly that may cause unsuccessful calibration.
Product
VITROS 250 Chemistry System, clinical chemistry analyzer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2216-2019·2019-08-14
MedComp Recalls Hemodialysis Catheter Kits Due to Labeling Error
Medical Components, Inc. is recalling 6,830 hemodialysis catheter insertion kits because the tray labels incorrectly describe the included introducer as valved.
Product
14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061424 Product Usage: An aid for introducing a hemodialysis catheter
Category
Medical Device
Distribution
Distributed nationwide