State

US Virgin Islands product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28576–28600 of 73774

HighFDA (Devices)·Z-2338-2020·2020-06-17
Philips Recalls IntelliSpace PACS 4.4 Due to Potential Image Corruption
Philips Healthcare Informatics is recalling 26 units of IntelliSpace PACS 4.4 because images may potentially become corrupt while using the system.
Product
IntelliSpace PACS 4.4, Product number 837507 - Product Usage: intended to be used by trained professionals, including but not limited to physicians, nurses and medical technicians.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20139·2020-06-17
Republic Wireless Recalls Relay Charging Cables Due to Overheating and Burn Hazards
Republic Wireless is recalling approximately 15,000 Relay charging cables sold between May 2018 and May 2019 because they can overheat and partially melt, posing a burn hazard.
Product
Charging Cable for Relay Screenless Communication Devices
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2282-2020·2020-06-17
Siemens ADVIA Chemistry Enzymatic Creatinine Recalled for Acetaminophen Interference
Siemens is recalling ADVIA Chemistry Enzymatic Creatinine reagents because acetaminophen metabolites may interfere with test results.
Product
ADVIA Chemistry Enzymatic Creatinine_2, Siemens Material Number 10335869, UDI Number 00630414526690 - Product Usage: use in the quantitative determination of creatinine in human serum, plasma, and urine for the diagnosis and treatment of renal disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2351-2020·2020-06-17
RayStation 9B Software Recall for Dose Calculation Errors
RaySearch Laboratories is recalling RayStation 9B Service Pack 1 due to a software error in dose calculation algorithms that could result in local underestimation of expected radiation dose.
Product
RayStation 9B Service Pack 1, UDI # 07350002010297 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2345-2020·2020-06-17
RayStation 8A Software Recall for Dose Calculation Error
RaySearch Laboratories is recalling RayStation 8A Service Pack 1 software due to a dose calculation error that could underestimate radiation therapy doses.
Product
RayStation 8A Service Pack 1, UDI # 07350002010136 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2354-2020·2020-06-17
Acuity A Link Z Spinal Fusion Device Recalled for Manufacturing Defect
Acuity Surgical Devices is recalling 178 A Link Z intervertebral body fusion devices because a manufacturing issue prevented bone screws from seating properly.
Product
A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Link Z Ti Unitary Plate-Cage 32x21x15 7 A Link Z Ti Unitary Plate-Cage 32x21x15 12 A Link Z Ti Unitary Plate-Cage 32x21x15 16 A Link Z Ti Unitary Plate-Cage 32x21x15 16 A Link Z Ti Unitary Plate-Cage…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2352-2020·2020-06-17
RayStation 6 Service Pack 1 Radiation Therapy Software Recall
RaySearch Laboratories is recalling RayStation 6 Service Pack 1 software due to a calculation error that may underestimate radiation dose.
Product
RayStation 6 Service Pack 1, UDI #s 07350002010037, 07350002010082 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2265-2020·2020-06-17
ROi CPS Recalls Custom Procedure Kits Containing Recalled BD Syringes
ROi CPS LLC is recalling 40 custom procedure kits because they contain PosiFlush Syringes from a lot previously recalled by BD.
Product
Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2350-2020·2020-06-17
RayStation 9B Software Recalled for Dose Calculation Error
RaySearch Laboratories is recalling RayStation 9B software due to a dose calculation error that could underestimate radiation therapy doses.
Product
RayStation 9B, UDI # 07350002010266 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2262-2020·2020-06-17
Ventana HE 600 Recalled for Electrical Short Risk
Ventana Medical Systems is recalling 461 HE 600 instruments due to a cleaning solution leak that can cause electrical shorts and burned components.
Product
Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System s intended use environment includes anatomic pathology (AP) laboratories and histology facilities within hospital, clinic, reference, or private lab settings. The System is to be operated by qualified…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2296-2020·2020-06-17
BioFire FilmArray BCID Panel Recalled for False Positive Proteus Results
BioFire Diagnostics is recalling FilmArray BCID Panels due to a risk of false positive Proteus results when used with specific blood culture media, which may lead to improper antibiotic treatment.
Product
FilmArray BCID Panel, RFIT-ASY-0127, 6, Rx Only, CE, IVD, UDI: 00815381020093 used with the following BACT/ALERT Blood Culture Bottle Catalog No./Description: 410851/BACT/ALERT¿ FA Plus 410852/BACT/ALERT¿ FN Plus 410853/BACT/ALERT¿ PF Plus 259790/BACT/ALERT¿ SN…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2355-2020·2020-06-17
Acuity Surgical Devices Recalls A Link Z Intervertebral Body Fusion Devices
Acuity Surgical Devices is recalling A Link Z Intervertebral Body Fusion Devices due to a manufacturing issue that may prevent vertebral body bone screws from seating properly.
Product
A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Link Z Ti Unitary Open Interbody 32x24x12 7 A Link Z Ti Unitary Open Interbody 32x24x12 12 A Link Z Ti Unitary Open Interbody 32x24x16 7 A Link Z Ti Unitary Open Interbody 32x24x16 12 Product Usage: is a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2298-2020·2020-06-17
HardyCHROM MRSA Recall for False Positive Results
Hardy Diagnostics is recalling HardyCHROM MRSA kits because they may produce false positive results for methicillin-susceptible Staphylococcus aureus.
Product
HardyCHROM MRSA,REF; G307, LOT: 447694, A selective and differential chromogenic medium for the qualitative direct detection of nasal colonization by methicillin-resistant Staphylococcus aureus (MRSA). Not intended to diagnose infection of guide therapy. Further testing required…
Category
Medical Device
Distribution
15 states
HighFDA (Drugs)·D-1306-2020·2020-06-17
Pfizer Recalls Unasyn Injection Due to Particulate Matter
Pfizer is recalling specific lots of Unasyn (ampicillin sodium and sulbactam sodium) for injection because particulate matter was identified after reconstitution.
Product
UNASYN — UNASYN (AMPICILLIN SODIUM AND SULBACTAM SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2284-2020·2020-06-17
Siemens Dimension Enzymatic Creatinine Recalled for Acetaminophen Interference
Siemens Healthcare Diagnostics is recalling Dimension Enzymatic Creatinine reagents because acetaminophen metabolites may interfere with test results.
Product
Dimension Enzymatic Creatinine, Siemens Material Number 10471520, UDI Number 00842768030512 - Product Usage: use in the quantitative determination of creatinine in human serum, plasma, and urine for the diagnosis and treatment of renal disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2325-2020·2020-06-17
Canon Medical System Recalls Infinix-8000V Catheterization Tables Due to Loose Bolts
Canon Medical System is recalling 46 Infinix-8000V systems because loose bolts may cause the catheterization table to tilt.
Product
Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2285-2020·2020-06-17
Siemens Dimension Vista Enzymatic Creatinine Recalled for Acetaminophen Interference
Siemens Healthcare Diagnostics is recalling Dimension Vista Enzymatic Creatinine test kits because acetaminophen metabolites may interfere with results.
Product
Dimension Vista Enzymatic Creatinine, Siemens Material Number 10700444, UDI Number 00842768036262 - Product Usage: use in the quantitative determination of creatinine in human serum, plasma, and urine for the diagnosis and treatment of renal disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2339-2020·2020-06-17
RayStation Radiation Therapy Software Recalled for Dose Calculation Error
RaySearch Laboratories is recalling RayStation software versions 4.0 to 5.0 Service Pack 2 due to a dose calculation error that may underestimate radiation dose.
Product
RayStation 4.0 to RayStation 5 Service Pack 2 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2302-2020·2020-06-17
Siemens Artis X-Ray Systems Recalled for Electrical Contact Issues
Siemens is recalling 15 Artis X-ray systems in the US because a power distributor defect may cause electrical contact interruptions, leading to procedure termination.
Product
Multi Display Manager in the Artis Systems (Image-Intensified Fluoroscopic X-Ray System) as follows: Artis Q floor Model: 10848280; Artis Q ceiling Model: 10848281; Artis Q biplane Model:10848282; Artis zee ceiling Model: 10094137; Artis zee floor Model…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2327-2020·2020-06-17
Canon Medical System Recalls Infinix-8000F Fluoroscopy Systems Due to Loose Bolts
Canon Medical System is recalling 15 Infinix-8000F digital radiography systems because loose bolts may cause the catheterization table to tilt.
Product
Infinix-8000F with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2328-2020·2020-06-17
Intuitive Surgical Recalls 8mm Endoscope Sterilization Trays Due to Sterility Risk
Intuitive Surgical is recalling 1,757 stainless steel reprocessing trays because holes in the sterilization wrap could compromise sterility and increase infection risk.
Product
STAINLESS STEEL REPROCESSING TRAY, 8MM ENDOSCOPE, IS4000, Model No. 400498-02 - Product Usage: is designed to enable complex surgery using a minimally invasive approach.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2300-2020·2020-06-17
Biomet Recalls Comprehensive VRS Inserter Shoulder Prosthesis Devices
Biomet is recalling 38 Comprehensive VRS Inserter shoulder prosthesis devices because the central screw drill may seize, potentially extending surgery time.
Product
Comprehensive VRS Inserter, shoulder prosthesis, Item No. 110019068. UDI: (01)00880304829503 (10)814100, (01)00880304829503 (10)570640, (01)00880304829503 (10)728890, (01)00880304829503 (10)977300
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2344-2020·2020-06-17
RayStation 8A Radiation Therapy Software Recalled for Dose Calculation Error
RaySearch Laboratories is recalling RayStation 8A software due to a defect in dose calculation algorithms that may underestimate radiation dose.
Product
RayStation 8A, UDI # 07350002010112 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2313-2020·2020-06-17
Biomet Recalls Proximal Humerus Plate Templates Due to Incomplete Design History
Biomet is recalling A.L.P.S. Proximal Humerus Plate Templates because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE 140MM Item Number: 110025472 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2357-2020·2020-06-17
BD FACS Sample Prep Assistant II Upgrade Recalled for Probe Wear
Becton, Dickinson and Company is recalling 51 units of the BD FACS Sample Prep Assistant II Upgrade due to premature probe wear that may cause sample dispensing issues.
Product
BD FACS Sample Prep Assistant (SPA) II Upgrade - Product Usage: K050191: The BD FACSCanto system with BD FACSCanto clinical software when used with the BD FACS Sample Prep Assistant II /III is intended for use as an in vitro diagnostic device for identification and enumeration…
Category
Medical Device
Distribution
Distributed nationwide