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.

56851–56875 of 74005

HighFDA (Devices)·Z-2733-2014·2014-10-08
Lumenis Array LaserLink Recall for Erroneous Retinal Pattern Display
Lumenis is recalling 16 Array LaserLink laser system accessories because they may project an incorrect pattern on the retina during treatment.
Product
Array LaserLink, Manufactured by Lumenis, The Array" LaserLink" is a laser system accessory intended for use in the treatment of ocular pathology. " For the Posterior Segment, the Array" LaserLink" is indicated for use in Retinal Photocoagulation and Panretinal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2731-2014·2014-10-08
Intuitive Surgical Recalls da Vinci Xi Patient Side Carts Due to Sensor Failure
Intuitive Surgical is recalling 75 da Vinci Xi Patient Side Carts because a motor sensor failure can occur after a mid-procedure restart.
Product
ASSEMBLY, PATIENT SIDE CART, PS4000 used with the da Vinci Xi Surgical System. Product Usage: The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive Surgical Endoscopic…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V630000·2014-10-08
Spartan Gladiator and MetroStar Emergency Vehicles Recalled for Seat Belt Defect
Spartan is recalling 2013-2015 Gladiator and MetroStar emergency vehicles because seat belts may be too long for smaller occupants, increasing crash injury risk.
Product
SPARTAN — SPARTAN GLADIATOR, METROSTAR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V632000·2014-10-08
Chrysler Recalls 2014 Minivans and Wranglers for Tire Pressure Software Error
Chrysler is recalling 2014 Town and Country, Grand Caravan, and Jeep Wrangler vehicles because a software error may prevent the tire pressure monitoring system from detecting low air pressure.
Product
DODGE — DODGE, JEEP, CHRYSLER GRAND CARAVAN, WRANGLER, TOWN AND COUNTRY
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2720-2014·2014-10-08
Siemens Dimension Vista CHEM 1 CAL Recall for Magnesium Calibration Error
Siemens is recalling Dimension Vista CHEM 1 CAL lot 3GM081 because it causes under-recovery of Magnesium in patient and QC samples.
Product
Siemens Dimension Vista¿ CHEM 1 CAL, lot 3GM081. The CHEM 1 CAL is an in vitro diagnostic product for the calibration of Calcium (CA), Cholesterol (CHOL), Creatinine (CREA), Glucose (GLU), Lactic Acid (LA), Magnesium (MG), Thyroxine (T4), Thyroxine Uptake (TU), Blood Urea…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1616-2014·2014-10-08
Actavis Recalls Diclofenac Sodium and Misoprostol Tablets Due to Splitting
Actavis is recalling 36,538 bottles of Diclofenac Sodium and Misoprostol tablets due to complaints of split or broken tablets.
Product
DICLOFENAC SODIUM AND MISOPROSTOL — DICLOFENAC SODIUM AND MISOPROSTOL (DICLOFENAC SODIUM AND MISOPROSTOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2728-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Caution Statements
Instrumed International is recalling 71 reusable laparoscopic instruments to add caution statements regarding voltage limits and product useful life.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0006-2015·2014-10-08
Recall of ENVOY 500 AST Reagent Kits Due to Quality Control Failures
ELITech Clinical Systems is recalling 878 ENVOY 500 AST Reagent Kits because quality control tests are failing before the products expire.
Product
ENVOY 500 AST Reagent Kit, reference Model/Catalog 55255, for Envoy 500. Intended Use of the Product: Envoy 500 AST Reagent is for the quantitative in vitro diagnostic determination of aspartate aminotransferase (AST) in human serum and plasma using the Envoy 500 Chemistry…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2724-2014·2014-10-08
Instrumed Recalls Reusable Laparoscopic Instruments for Updated Safety Instructions
Instrumed International is recalling 3,093 reusable laparoscopic instruments to add caution statements regarding voltage limits and useful life to the Instructions For Use.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2727-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions
Instrumed International is recalling 895 reusable laparoscopic instruments to add caution statements regarding voltage limits and product life to the Instructions For Use.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2730-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Warnings
Instrumed International is recalling reusable laparoscopic instruments to add caution statements regarding voltage limits and product useful life.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2734-2014·2014-10-08
Baro-Therapies Rejuvenator Chamber Recalled for Lack of FDA Approval
Baro-Therapies, Inc. is recalling 10 Rejuvenator Chambers because they were distributed without an approved 510(k).
Product
The Rejuvenator Chamber manufactured by Baro-Therapies, Inc. Product Usage: Indicated for relief from general aches and pains brought on by changes in the weather.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2723-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Caution Statements
Instrumed International is recalling 156 reusable laparoscopic instruments to add caution statements regarding voltage limits and useful life to the Instructions For Use.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2725-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions
Instrumed International is recalling 83 reusable laparoscopic instruments to add caution statements regarding voltage limits and product useful life.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0009-2015·2014-10-08
Gendex eXpertDC Intraoral X-Ray Recall for Spring Link Failures
Gendex Corp is recalling 651 eXpertDC intraoral x-ray units worldwide because spring link components in the articulated arm assembly broke during normal assembly.
Product
eXpertDC intraoral x-ray, models: eXpert DC, NA, 75 Inch reach; eXpert DC, NA, 65 Inch reach; eXpert DC, CN, 55 Inch reach; eXpert DC, WW, 75 Inch reach; eXpert DC, WW, 65 Inch reach; eXpert DC, WW, 55 Inch reach; OEM Arm Assembly w/o cables; Assy, Articulated Arm & Tubehead…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2736-2014·2014-10-08
Nanosphere Recalls Verigene BC-GN Kits Due to Processing Error Risk
Nanosphere is recalling Verigene BC-GN Kits because a specific lot of extraction trays may cause processing errors in the device.
Product
Verigene BC-GN Kit (Catalog number 20-005-021); 1) 20 Verigene BC-GN Test Cartridges; are qualitative multiplexed in vitro diagnostic tests for simultaneous detection and identification of selected gram-positive (BC-GP) and gram-negative (BC-GN) bacteria and resistance markers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0007-2015·2014-10-08
Ortho-Clinical Diagnostics Recalls VITROS Phenytoin Slides Due to Potential Bias
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products PHYT Slides because they may produce biased results, potentially affecting patient care.
Product
VITROS Chemistry Products PHYT (Phenytoin) Slides, REF/Product Code 829 8671, IVD. For in vitro diagnostic use only. VITROS Chemistry Products PHYT Slides quantitatively measure phenytoin (PHYT) concentration in serum and plasma using VITROS 250/350/950/5,1 FS and 4600…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2729-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions
Instrumed International is recalling 15 reusable laparoscopic instruments to add caution statements regarding voltage limits and product life to the Instructions For Use.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2735-2014·2014-10-08
Nanosphere Verigene BC-GP Kit Extraction Tray Recall
Nanosphere is recalling Verigene BC-GP Kit extraction trays because a specific lot may cause processing errors and tips to drop into the processor.
Product
Verigene BC-GP Kit (Catalog number 20-005-018); 1) 20 Verigene BC-GP Test Cartridges; are qualitative multiplexed in vitro diagnostic tests for simultaneous detection and identification of selected gram-positive (BC-GP) and gram-negative (BC-GN) bacteria and resistance markers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0010-2015·2014-10-08
GE Healthcare Precision 500D X-ray Systems Recalled for Missing Screws
GE Healthcare is recalling Precision 500D X-ray systems because missing screws may cause the overhead video monitor to detach from the tray assembly.
Product
GE Healthcare Precision 500D, Classical R&F System. Product Usage: The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and Pediatric examinations.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2722-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions
Instrumed International is recalling reusable laparoscopic instruments to add caution statements regarding voltage limits and product life.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2721-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions
Instrumed International is recalling 65 reusable laparoscopic instruments to add caution statements regarding voltage limits and useful life to the Instructions For Use.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1617-2014·2014-10-08
Actavis Recalls Diclofenac Sodium and Misoprostol Tablets Due to Splitting
Actavis is recalling 6,041 bottles of Diclofenac Sodium and Misoprostol tablets because they may be split or broken.
Product
DICLOFENAC SODIUM AND MISOPROSTOL — DICLOFENAC SODIUM AND MISOPROSTOL (DICLOFENAC SODIUM AND MISOPROSTOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2726-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions
Instrumed International is recalling 122 reusable laparoscopic instruments to add caution statements regarding voltage limits and product life to the Instructions For Use.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2717-2014·2014-10-08
KCI CelluTome Epidermal Harvesting System Recalled Due to Blade Shift
KCI USA, Inc. is recalling 1,331 units of the CelluTome Epidermal Harvesting System because the blade can shift during shipping, rendering the product ineffective.
Product
CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number CT-H50
Category
Medical Device
Distribution
Distributed nationwide