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.

58001–58025 of 74005

HighFDA (Devices)·Z-1927-2014·2014-07-02
Siemens Healthcare Recalls ADVIA Acid/Base Reagent Kits Due to Metal Contamination
Siemens Healthcare is recalling ADVIA Acid/Base Reagent 1 and 2 Kits because trace metal contamination caused the acid bottles to swell.
Product
Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing ADVIA Centaur Acid Reagent bottles, lot number: 454778 Kit Catalog Number: 112219 SMN: 10310026 Intended Use: In vitro diagnostic use. Acid Regent is a component of the ADVIA Centaur and ADVIA Centaur XP…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14222·2014-07-02
All Power America Recalls Single Stage Snow Throwers Due to Fire Hazard
All Power America is recalling about 10,000 single stage snow throwers because a corroded carburetor needle can cause fuel leaks, posing a fire hazard.
Product
Single Stage Snow Thrower
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1867-2014·2014-07-02
Siemens StreamLAB Analytical Workcell Recalled for Trip and Fall Hazard
Siemens is recalling 317 StreamLAB Analytical Workcells because protruding pins on the Input/Output Module have contributed to trip and fall incidents.
Product
Siemens StreamLAB(R) Analytical Workcell; Catalog number 746002.901. Designed to automate sample handling and processing in the clinical laboratory.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V417000·2014-07-02
GM Recalls 2012-2014 Vehicles for Damaged Block Heater Cords
General Motors is recalling specific 2012-2014 Buick and Chevrolet vehicles because insulation on the engine block heater cord can damage in cold weather, exposing wires.
Product
CHEVROLET — CHEVROLET, BUICK SONIC, VERANO, CRUZE, ENCORE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1857-2014·2014-07-02
NxStage Dialysate Sacks Recalled for Excess Aluminum Levels
NxStage Medical is recalling dialysate sacks with concentrate due to aluminum levels exceeding internal product specifications.
Product
NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-304 Lactate 45, Potassium 2, Sodium 140, Calcium 3,Magnesium 1, Chloride 101, Glucose (mg/dL) 100 Batch Size (liters) 60 The SAK is one of the disposables used with NxStage PureFlow SL…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1869-2014·2014-07-02
Elekta MOSAIQ Oncology System Recalled for Dose Calculation Error
Elekta, Inc. is recalling MOSAIQ oncology information system software because it fails to recalculate agent volume when users change the ordering dose.
Product
MOSAIQ MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be used where ever radiotherapy and/or chemotherapy are prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1858-2014·2014-07-02
NxStage Dialysate Sacks Recalled for Excess Aluminum Levels
NxStage Medical is recalling dialysate sacks with concentrate due to aluminum levels exceeding internal product specifications.
Product
NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-305 Lactate 45, Potassium 1, Sodium 140, Calcium 3, Magnesium 1 Chloride 100, Glucose (mg/dL) 100 Batch Size (liters) 40
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1844-2014·2014-07-02
Puritan Bennett 840 Ventilator Recall for Display Loss
Nellcor Puritan Bennett is recalling 104 Puritan Bennett 840 Ventilators due to reports of loss of graphical user interface display information while the device continues to provide breath support.
Product
Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or non-invasive ventilatory support and monitoring for infant, pediatric, and adult patients with respiratory failure or respiratory insufficiency. It is used in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1848-2014·2014-07-02
SteriGear Recalls Urinary Drain Bags Due to Valve Malfunction
SteriGear is recalling 110,560 urinary drain bags because the valve can close and create negative pressure, potentially blocking urine flow.
Product
SteriGear Urinary Drain Bag with Fig Leaf Cover, 2000 ml, REF 10270, The Fig Leaf, SteriGear 362 S. University Avenue, provo, UT 84601, 1-800-398-3259, SteriGear.com, Sterile, EO Urinary Drainage Collection Kit, for Indwelling Catheter. This device is intended to collect the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1849-2014·2014-07-02
Western VIPR Pressure Regulators Recalled for Cylinder Separation Risk
Western / Scott Fetzer Company is recalling Model RG3000 and RG4000 Series Valve Integrated Pressure Regulators (VIPR) because they may separate from aluminum cylinders.
Product
Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14221·2014-07-02
Porter-Cable Fixed-Base Production Routers Recalled for Electrical Shock Hazard
Porter-Cable is recalling fixed-base production routers and bases because the handles lack insulation, posing an electrical shock risk. No injuries have been reported.
Product
Fixed-base routers and router bases
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1926-2014·2014-07-02
Siemens Dimension LOCI Troponin I Calibrator Recalled for Result Shifts
Siemens is recalling Dimension LOCI Troponin I Calibrators because they may cause a 24% upward shift in test results.
Product
Siemens Dimension LOCI TNI Troponin I Calibrator RC 621. The LOCI TNI Troponin I Calibrator is an in vitro diagnostic product for the calibration of the cardiac troponin I (TNI) method for the Dimension clinical EXL integrated chemistry system with LOCI module.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1868-2014·2014-07-02
Integra Recalls Accell Evo3C Bone Matrix Due to Packaging Error
Integra LifeSciences is recalling 61 units of Accell Evo3C Demineralized Bone Matrix because they were incorrectly packaged in boxes for a different product, creating a risk of improper surgical use.
Product
Accell Evo3C Demineralized Bone Matrix, 5 cc, Model Number: 02-6000-050 , Lot Number: 132160. Product Usage: Accell Evo3c Demineralized Bone Matrix Putty is intended for filling voids and gaps in the skeletal system that are not intrinsic to the stability of the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1851-2014·2014-07-02
Teleflex Medical Recalls RUSCH LaserTube Tracheal Tubes for Missing Latex Warning
Teleflex Medical is recalling RUSCH LaserTube tracheal tubes because the label failed to print a specific caution statement regarding natural rubber latex.
Product
RUSCH, LaserTube (Rubber), Laser Resistant Tracheal Tube, cuffed, Teleflex Medical, Willy-Rusch, GmbH. A tracheal tube is a device inserted into a patient's trachea via the nose or mouth and used to maintain an open airway.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1745-2014·2014-07-02
Philips Brilliance CT Big Bore Recalled for Radio Frequency Emission Tolerance Issues
Philips is recalling 454 Brilliance CT Big Bore systems because internal testing found radio frequency emissions exceeded IEC 60601-1-2 standards.
Product
Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray System & Brilliance CT Big Bore Radiology Whole Body Computed Tomography X-Ray System. Product Usage: The Brilliance CT Big Bore is a Whole Body Computed Tomography X-Ray System which produces…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2043-2014·2014-07-02
Princess House Tangerine Appetizer Plate Set Recalled for Cadmium Leaching
Princess House Inc. is recalling 11,912 sets of Marissa Collection Tangerine Appetizer Plates because they leach cadmium above acceptable levels.
Product
Marissa Collection Tangerine Appetizer Plate Set (set of 2). distributed by Princess House Inc., Taunton, MA
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1840-2014·2014-07-02
Siemens LANTIS System Recall for Unvalidated Operating System Risks
Siemens is recalling 108 LANTIS linear accelerator systems because using the software with unvalidated operating systems can cause data corruption and incorrect treatment records.
Product
Siemens LANTIS System ; LANTIS Commander, 10 Users ; LANTIS 6.1 Commander ; LANTIS 8.3 Commander The intended use of the linear accelerator is to deliver x-ray radiation for therapeutic treatment of cancer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1855-2014·2014-07-02
NxStage Dialysate Sacks Recalled for Excess Aluminum Levels
NxStage Medical is recalling dialysate sacks used in dialysis systems because they contain aluminum levels exceeding internal specifications.
Product
NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-302 Lactate , 40, Potassium 1, Sodium 140, Calcium 3, Magnesium 1, Chloride 105, Glucose (mg/dL) 100, Batch Size (liters): 60 The SAK is one of the disposables used with NxStage PureFlow SL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1843-2014·2014-07-02
BioFire FilmArray Blood Culture Identification Panel Recalled for False Positives
BioFire is recalling the FilmArray Blood Culture Identification Panel due to an increased risk of false positive results when used with specific blood culture bottles.
Product
FirmArray Blood Culture Identification (BCID) Panel, Model 2.0 The FilmArray Blood Culture Identification (BCID) Panel is a qualitative multiplexed nucleic acid-based in vitro diagnostic test designed to test positive blood cultures to quickly identify the organism that is…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1864-2014·2014-07-02
Philips Ingenia 3.0T MRI Systems Recalled for Incorrect Hardware
Philips is recalling 18 Ingenia 3.0T MRI systems because incorrect M10 nuts were used instead of stainless steel nuts.
Product
Ingenia 3.0T, magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1862-2014·2014-07-02
Philips Ingenia 3.0T MRI Systems Recalled for Incorrect Nut Components
Philips is recalling 21 Ingenia 3.0T MRI systems because some were shipped with incorrect M10 nuts instead of A4 stainless steel nuts.
Product
Ingenia 3.0T R5, magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1845-2014·2014-07-02
Siemens RAD Fluoro Uro System Recalled for Image Malfunction
Siemens is recalling 76 RAD Fluoro Uro Systems because a software malfunction can cause images to appear very dark, potentially leading to unnecessary repeat examinations.
Product
Siemens RAD Fluoro Uro System (Ysio, Luminos dRF, and Uroskop Omnia) with software versions VB10G. Product Usage: Image Intensified Fluoroscopic X-ray system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1861-2014·2014-07-02
NxStage Dialysate Sack Recalled for Excess Aluminum Levels
NxStage Medical is recalling 91 cases of dialysate sacks because aluminum levels exceeded internal specifications. The product was distributed in the US and internationally.
Product
NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-407 Lactate 40, Potassium 1, Sodium 140, Calcium 3, Magnesium 1, Chloride 105, Glucose (mg/dL) 100 Batch Size (liters) 50
Category
Medical Device
Distribution
Distributed nationwide
ModerateNHTSA·14V406000·2014-07-02
Ford Recalls 2014 Transit Connect Vehicles for Missing Brake Fluid Label
Ford is recalling 2014 Transit Connect vehicles because the brake reservoir cap may lack required text identifying the correct brake fluid. This non-compliance could lead to incorrect fluid usage and brake system damage.
Product
FORD — FORD TRANSIT CONNECT
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1847-2014·2014-07-02
Baxter Abacus 3.1 Pharmacy Calculator Software Field Correction
Baxter is correcting a software error in Abacus 3.1 that may display protein levels 1,000 times lower than actual when using Clinimix 4.25110.
Product
Abacus 3.1, Pharmacy Calculator Product Usage: Provide pharmacy calculations for automated compounding.
Category
Medical Device
Distribution
Distributed nationwide