State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58251–58275 of 74005

SevereFDA (Devices)·Z-1706-2014·2014-06-11
GE Healthcare Recalls Kenex Ceiling Suspended Radiation Shields and Lamps
GE Healthcare is recalling Kenex ceiling suspended radiation shields and surgical lamps due to improper installation. A reported incident involved a shield falling from the ceiling.
Product
Kenex Radiation Shield and surgical lamps installed with GE Healthcare Interventional, Surgery, CT and X-Ray Imaging systems. Kenex Suspension installed with Radiation shield and lamp with following model numbers…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1719-2014·2014-06-11
ConMed Recalls MACROLYTE Premie Dispersive Electrodes Due to Sparking and Burning
ConMed Corporation is recalling MACROLYTE Premie Dispersive Electrodes due to confirmed complaints of sparking, no output, and burning at the cord set connection.
Product
MACROLYTE Premie Dispersive Electrode, REF 440-2400, CONMED CORPORATION. The device is applied to the patient during electrosurgical procedures to provide a path for RF current to leave the patient and return to the generator.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1714-2014·2014-06-11
Toshiba Infinix X-Ray System Recalled for Table Movement Safety Issue
Toshiba is recalling two Infinix X-Ray Interventional Systems because the table may continue moving during longitudinal tilt despite error signals.
Product
Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system that is capable of radiographic and fluoroscopic studies used in an interventional setting.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1712-2014·2014-06-11
Microport Recalls PATH Thread Cup Adaptors Due to Removal Difficulty
Microport Orthopedics is recalling 140 units of PATH Thread Cup Adaptors because they may be difficult to remove from the impaction handle during surgery.
Product
PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc. Orthopaedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1721-2014·2014-06-11
Siemens CT Systems Recalled Due to Rubber Damper Degradation Risk
Siemens Medical Solutions is recalling 345 CT systems because a rubber damper may degrade and break, potentially causing motor mounting plates to loosen and injuring operators or patients.
Product
Siemens SOMATOM Emotion 16, Emotion 6, and SOMATOM Spirit Computed Tomography Systems Product Usage: To produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1699-2014·2014-06-11
Cochlear Baha Soft Tissue Gauge Recalled for Metal Surface Imperfections
Cochlear Americas Inc. is recalling 288 Baha Soft Tissue Gauges due to manufacturing imperfections that could leave residual metal on patient skin.
Product
Cochlear Baha Soft tissue gauge 6mm. Reusable instrument used to ensure the soft tissue thickness is equal to or less than 6 mm. For use with Baha Attract hearing system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1713-2014·2014-06-11
Arrow Percutaneous Sheath Introducer Kits Recalled for Dilator Tip Damage
Arrow International Inc is recalling specific Percutaneous Sheath Introducer Kits due to dilator tip damage that could cause vessel injury.
Product
Arrow¿ Percutaneous Sheath Introducer Kits The Percutaneous sheath introducer products permit venous or arterial access and device introduction to the central circulation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1703-2014·2014-06-11
Hospira Infusion Pumps Recalled for Door Roller Assembly Defect
Hospira is recalling specific Plum XL and Micro Macro infusion pumps because a door roller assembly may break, preventing the cassette from locking properly.
Product
Plum XL, Micro Macro Plum XL3 with data port, and Micro Macro Plum XL with data port infusion pumps, indicated for intravenous, arterial, short-term epidural, and parenteral administration of general I.V. fluids, medications, nutritional fluids, and blood/blood products to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1690-2014·2014-06-11
FDA Recalls Bard Ventralight ST Mesh Due to Potential Sterility Compromise
Davol, Inc. is recalling specific lots of Bard Ventralight ST Mesh because the sterile packaging may be open or have a weak seal, potentially compromising sterility.
Product
Bard¿ Ventralight" ST Mesh with Echo PS" 4"x6" Reorder Number: 5955460 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1678-2014·2014-06-11
Philips IntelliSpace Portal Software Recall for SPECT Reconstruction Errors
Philips Medical Systems is recalling IntelliSpace Portal software because SPECT reconstructions may lack scatter correction or apply resolution recovery incorrectly.
Product
IntelliSpace Portal (ISP), (ISP DX/HX/EX, Model number 881001; ISP IX, Model number 881030; ISP LX SPECT, Model number 881035), Philips Medical Systems. A medical software system for diagnostic imaging data viewing.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1694-2014·2014-06-11
Bard Ventralight ST Mesh Recall Due to Potential Sterility Compromise
Davol, Inc. is recalling Bard Ventralight ST Mesh because the sterile inflation assembly pouch may be open or have a weak seal.
Product
Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Number: 5955790 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V313000·2014-06-11
Blue Bird Recalls 2008-2013 All American School Buses for Thermostat Defect
Blue Bird is recalling 2008-2013 All American school buses because a thermostat design flaw may cause a heater hose to rupture, allowing hot coolant to enter the passenger compartment.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1702-2014·2014-06-11
Hospira Recalls LifeCare 5000 Infusion Pumps Due to Door Roller Defect
Hospira is recalling LifeCare 5000 infusion pumps because a broken door roller pin may prevent the door from locking the cassette properly, potentially causing alarms or false occlusions.
Product
LifeCare 5000 Pump (Plum 1.6) infusion pump, indicated for volumetric infusion of critical drugs and fluids by intravenous (I.V.) administration.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1722-2014·2014-06-11
Philips CT Scanners Recalled for Disengaged Service Latch
Philips Medical Systems is recalling 6,839 CT scanners worldwide because a service latch may disengage, causing the table top to become free-floating.
Product
Philips Medical Systems Computed Tomography X-ray systems (Brilliance CT series, iCT, iCT SP, Ingenuity CT, Ingenuity Core, Ingenuity Core128, Ingenuity Flex, and the MX8000 Dual v. EXP scanners)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1673-2014·2014-06-11
Bayer Medrad Continuum MR Infusion System Recall for Damaged Locking Pins
Bayer is recalling non-wireless Medrad Continuum MR Infusion Systems shipped before March 2008 due to potentially damaged locking pins in the bracket.
Product
Medrad Continuum MR Infusion system- non-wireless system The MEDRAD Continuum MR Infusion System is designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior to, during and immediately…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1708-2014·2014-06-11
CP Medical Recalls Monoswift PGCL Sutures for Tensile Strength Failure
CP Medical is recalling one lot of Monoswift PGCL absorbable sutures because they failed to meet USP minimum tensile strength requirements.
Product
Monoswift¿ PGCL [poly (glycolide-co-caprolactone)] Absorbable Surgical Suture; USP size 3/0 PGCL; part number L936. Product is labeled sterile. The product is sealed inside an inner foil pouch with an outside Tyvek¿ pouch. It is an undyed, monofilament synthetic absorbable…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1686-2014·2014-06-11
Bard Composix LIP Mesh Recall Due to Potential Sterility Compromise
Davol, Inc. is recalling Bard Composix LIP Mesh with Echo PS because the sterile inflation assembly packaging may be open or have a weak seal.
Product
Bard¿ Composix" LIP Mesh with Echo PS" 8"x10" Reorder Number: 0144810 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1707-2014·2014-06-11
Brainlab ExacTrac 5.5 Image Processing System Recalled for Plan Blending Error
Brainlab AG is recalling ExacTrac 5.5 image processing systems because a specific workflow may generate unintended blends of separate patient treatment plans.
Product
ExacTrac 5.5, an Image Processing System used for patient positioning for radiation therapy or radiosurgery.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V314000·2014-06-11
Blue Bird Recalls 2008-2013 All American Buses for Heater Hose Rupture Risk
Blue Bird is recalling 2008-2013 All American rear engine non-school buses because a heater hose may rupture, allowing hot coolant to enter the passenger compartment.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·14204·2014-06-11
Cost Plus Recalls Glass Bubble Knobs Due to Laceration Hazard
Cost Plus is recalling glass bubble knobs sold at World Market stores because they can break and cause hand or finger lacerations.
Product
Glass Bubble Knobs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1717-2014·2014-06-11
Siemens Ysio Systems Recalled for Potential Unintended Radiation Release
Siemens is recalling 433 Ysio radiographic systems because excessive cleaning liquid usage may cause a short circuit, leading to unintended radiation release.
Product
Siemens Ysio Systems Product Usage: The Ysio (New RAD-FAMILY) systems are radiographic systems used in hospitals, clinics, and medical practices. Ysio enables radiographic and tomographic exposures of the whole body including: skull, chest, abdomen, and extremities and may…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1704-2014·2014-06-11
Hospira Recalls Infusion Pumps Due to Door Roller Assembly Breakage Risk
Hospira is recalling specific Plum XL and LifeCare infusion pumps because a door roller assembly may break, preventing the cassette door from locking properly.
Product
Plum XL3 Multi line Infusion System, Micro Macro Plum XL3 Multi line Infusion System, and Micro Macro Plum XL Infusion System. Infusion pumps for intravenous. arterial, short-term epidural, and parenteral administration of general I.V. fluids, medications, nutritional fluids…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1688-2014·2014-06-11
Bard Ventralight ST Mesh Recall Due to Potential Pouch Seal Failure
Davol, Inc. is recalling Bard Ventralight ST Mesh with Echo PS due to potential pouch seal failures that could compromise sterility.
Product
Bard¿ Ventralight" ST Mesh with Echo PS" 12"x14" Reorder Number: 5955124 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1360-2014·2014-06-11
CareFusion Recalls Surgical Scrub Brushes With Low Iodine Levels
CareFusion is recalling surgical scrub brushes because the available iodine content is lower than stated on the label.
Product
CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 15% Povidone-iodine (USP) Surgical Hand Scrub; CareFusion, Vernon Hills, IL 60061 USA, NDC 57613-013-15.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1720-2014·2014-06-11
Small Bone Innovations Recalls Non-Sterile RingFIX Olive Wires
Small Bone Innovations is recalling non-sterile RingFIX Olive Wires because they were packaged with the wrong internal component.
Product
SBi RingFix Olive Wires Product Usage: These are temporary devices indicated for: osteosynthesis of fractures with small osteoarticular fragments, fixation of open and closed fractures, arthrodesis, sepsis, limb lengthening, and osteotomy.
Category
Medical Device
Distribution
Distributed nationwide