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.

32326–32350 of 73900

HighFDA (Devices)·Z-2400-2019·2019-09-04
Siemens SOMATOM go.Up CT Systems Recalled for Falling Injector Holder
Siemens is recalling 18 SOMATOM go.Up CT systems because the injector holder could fall off, posing a risk of injury.
Product
SOMATOM go.Up; Models #11061620 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2390-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397190, 14.5F, straight, 19cm length, BARD, UDI: 00801741012297
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2387-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter, REF/Product code:5396190, 14.5F, Alphacurve, 19cm length, BARD, UDI: 00801741012242
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2392-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recall Due to Tip Damage
Bard Peripheral Vascular Inc is recalling 887 units of GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397270, 14.5F, straight, 27cm length, BARD, UDI: 00801741012310
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2385-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393270, 14.5F, Straight, 27cm length, BARD, UDI: 00801741012198
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2374-2019·2019-09-04
Bard Equistream Hemodialysis Catheter Recalled for Molded Tip Defect
Bard Peripheral Vascular Inc is recalling 13 units of Equistream Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Product
EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5903310, 14.5F, Straight ,31cm length, BARD, UDI: 00801741013720
Category
Medical Device
Distribution
53 states
ModerateFDA (Devices)·Z-2423-2019·2019-09-04
Stryker Endotrac Hook Blade Recalled for Compromised Sterile Bag Seal
Stryker GmbH is recalling 110 units of Endotrac EPF/EGR Hook Blades because the sterile bag seal integrity may be compromised.
Product
Endotrac EPF/EGR Hook Blade, Angled, Catalog Number 3055A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2414-2019·2019-09-04
Stryker Endotrac ECTR Triangle Blade Recalled Due to Compromised Sterile Bag Seal
Stryker GmbH is recalling 53 Endotrac ECTR Triangle Blades because the sterile bag seal may be compromised, potentially affecting sterility.
Product
Endotrac ECTR Triangle Blade, Catalog Number 2054-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2424-2019·2019-09-04
Stryker Recalls Endintrak 2 Hook Blade Kits Due to Seal Integrity
Stryker GmbH is recalling 259 Endintrak 2 Hook Blade kits because the sterile bag seal integrity may be compromised, potentially affecting sterility.
Product
Endintrak¿ 2 Hook Blade, Angled, Catalog Number 4058A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2415-2019·2019-09-04
Stryker Recalls Endotrac ECTR Hook Blades Due to Seal Integrity Concerns
Stryker GmbH is recalling 1,959 Endotrac ECTR Hook Blades because the sterile bag seal may be compromised, potentially affecting sterility.
Product
Endotrac ECTR Hook Blade, Catalog Number 2055-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2408-2019·2019-09-04
Ad-Tech Skull Anchor Bolts Recalled for Incorrect MRI Approval Labeling
Ad-Tech Medical Instrument Corporation is recalling Skull Anchor Bolts because supplemental information incorrectly indicated they were approved for use in the MR environment.
Product
Skull Anchor Bolts
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2396-2019·2019-09-04
Ad-Tech Spencer Probe Depth Electrodes Recalled for Incorrect Contact Count Labeling
Ad-Tech Medical Instrument Corporation is recalling 18 Spencer Probe Depth Electrodes because two units labeled as 8-contact were actually 6-contact. No patient impact was reported.
Product
AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth Electrodes (Depth Electrodes, Foramen Ovale Depth Electrodes, Macro Micro Depth Electrodes, Spencer Probe Depth Electrodes, Wyler Sphenoidal Depth Electrodes) are intended for temporary (< 30 days) use…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2406-2019·2019-09-04
Ad-Tech Medical Recalls Subdural Electrodes Due to Incorrect MR Safety Labeling
Ad-Tech Medical Instrument Corporation is recalling subdural electrodes because supplemental information incorrectly stated they were approved for use in MRI environments.
Product
Dual-Sided Interhemispheric, Grid, Intraoperative, Strip, Wyler Subdural Electrodes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2420-2019·2019-09-04
Stryker Recalls Endotrac ECTR Triangle Blades Due to Seal Integrity
Stryker GmbH is recalling 94 Endotrac ECTR Triangle Blades because the sterile bag seal may be compromised, potentially affecting sterility.
Product
Endotrac ECTR Triangle Blade, Angled, Catalog Number 2054A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2407-2019·2019-09-04
Ad-Tech Medical Recalls Depth Electrodes Due to Incorrect MR Safety Labeling
Ad-Tech Medical Instrument Corporation is recalling depth electrodes because supplemental information incorrectly stated they were approved for use in the MR environment.
Product
Depth Electrodes, Foramen Ovale Depth Electrodes, Macro Micro Depth Electrodes, Spencer Probe Depth Electrodes, Wyler Sphenoidal Depth Electrodes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2416-2019·2019-09-04
Stryker Endotrac Push Blade Recalled for Compromised Sterile Bag Seal
Stryker GmbH is recalling 251 Endotrac EPF/EGR Push Blades because the sterile bag seal integrity may be compromised.
Product
Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2421-2019·2019-09-04
Stryker Recalls Endotrac ECTR Hook Blade Kits Due to Seal Integrity
Stryker GmbH is recalling 28 Endotrac ECTR Hook Blade kits because the sterile bag seal integrity may be compromised.
Product
Endotrac ECTR Hook Blade, Angled, Catalog Number 2055A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2365-2019·2019-09-04
Bausch & Lomb Recalls Laseredge 1.1mm Arrow Knife Due to Dull Edge
Bausch & Lomb is recalling Laseredge 1.1mm Arrow Knives used in ophthalmic surgery because the knife edge may be dull.
Product
Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2412-2019·2019-09-04
Stryker Recalls Endotrig ETF Hook Blades Due to Sterile Seal Concerns
Stryker GmbH is recalling 35 Endotrig ETF Hook Blades because the sterile bag seal integrity may be compromised, potentially affecting sterility.
Product
Endotrig ETF Hook Blade, Catalog Number 1052-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2418-2019·2019-09-04
Stryker Endotrac Hook Blade Recalled for Compromised Sterile Bag Seal
Stryker GmbH is recalling 2,248 Endotrac EPF/EGR Hook Blades because the sterile bag seal may be compromised, potentially affecting sterility.
Product
Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2358-2019·2019-09-04
Medline Recalls Sterile Piston Irrigation Syringe Trays Due to Packaging Defects
Medline Industries is recalling 11,962 sterile piston irrigation syringe trays because samples showed incomplete or open packaging seals.
Product
Medline SYRINGE, PISTON,IRR TRAY,W/.9, REF DYNC2303. Sterile Piston Irrigation Syringe Tray with Saline
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2432-2019·2019-09-04
Baxter Recalls Exactamed Oral Dispensers Due to Mixed Sizes
Baxter Healthcare is recalling Exactamed 5 mL Oral Dispensers because pharmacy packs may contain 10 mL dispensers.
Product
EXACTAMED Oral Dispensers, 5mL, AMBER: PHARMACY PACK, REF H9388505, x500 PHARMACY PACK, REF H9388105, x100 COST CONTAINMENT, REF H93884205, x1500
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2397-2019·2019-09-04
Phadia 1000 Immunodiagnostic Instruments Recalled for Liquid Sensor Error
Phadia Ab is recalling 387 Phadia 1000 immunodiagnostic instruments due to a liquid sensor error. The recall affects facilities in 27 US states.
Product
Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including software for immunodiagnostic testing. The instrument is designed to handle all steps from sample and reagent handling to processing of results.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2359-2019·2019-09-04
Agilent MassHunter Software Recall Due to Sample Data Mismatch
Agilent Technologies is recalling MassHunter Quantitative Analysis Software versions B.07 or below due to a defect that causes sample name mismatches and prevents saving changes.
Product
MassHunter Quantitative Analysis Software, Version B.07.01, used with Triple Quadrupole Mass Spectrometers, models K6460 and K6420 Product Usage: A mass spectrometer for clinical use is a device intended to identify inorganic or organic compounds (e.g., lead, mercury, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2366-2019·2019-09-04
Bausch & Lomb Recalls Laseredge Knives Due to Possible Dull Edge
Bausch & Lomb is recalling specific Laseredge Knives used in ophthalmic surgery because they may have dull edges.
Product
Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED, REF E7599 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide