State

US Virgin Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36901–36925 of 73915

HighFDA (Devices)·Z-3217-2018·2018-10-03
Philips INTEGRIS Allura 15-12 Biplane Monitor Suspension Recall
Philips is recalling INTEGRIS Allura 15-12 biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
INTEGRIS Allura 15-12 (biplane), System Code 722044 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3239-2018·2018-10-03
Philips Medical Monitor Ceiling Suspension Recall Due to Detachment Risk
Philips is recalling 5,115 medical monitor ceiling suspensions because the monitor may detach and fall, posing an injury risk to patients and users.
Product
Cesar Powerpack-Visub(V3000), System Code 72243 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3254-2018·2018-10-03
Intuitive Surgical Recalls da Vinci Redundant Medical Grade Power Supply Units
Intuitive Surgical is recalling specific da Vinci Surgical System power supply units that were manufactured incorrectly and may fail during use.
Product
da Vinci Si/X/Xi Surgical System Redundant Medical Grade Power Supply (RMGPS) Units The da Vinci System consists of a Surgeon Console, a Patient Cart, and a Vision Cart and is used with an endoscope, da Vinci EndoWrist instruments, and accessories to perform minimally…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3214-2018·2018-10-03
Philips INTEGRIS Allura 9 Biplane Recall for Monitor Suspension Defect
Philips is recalling INTEGRIS Allura 9 biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
INTEGRIS Allura 9 (biplane), System Code 722021 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3240-2018·2018-10-03
Stryker Recalls Hoffmann LRF Hexapod Software Due to Calculation Error
Stryker GmbH is recalling 233 units of Hoffmann LRF Hexapod Software because it may compute erroneously accelerated correction plans under specific settings.
Product
Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: HLRF 1.0-2/002, HLRF 1.1-2/002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1217-2018·2018-10-03
Boehringer Ingelheim Recalls SYNJARDY Tablets Due to Cross Contamination
Boehringer Ingelheim is recalling 998 bottles of SYNJARDY tablets due to cross-contamination with other products.
Product
SYNJARDY — SYNJARDY (EMPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3243-2018·2018-10-03
Terumo Advanced Perfusion System Power Manager Board Recall
Terumo is recalling 10 Advanced Perfusion System units due to improperly torqued screws on the Power Manager Board, which may cause electrical shorts.
Product
Terumo 220/240V AC, Advanced Perfusion System Platform (APS) for use in cardiopulmonary bypass procedures. Catalog Number 801764
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3222-2018·2018-10-03
Philips Allura Xper FD2O Monitor Ceiling Suspension Recall
Philips is recalling Allura Xper FD2O systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper FD2O, System Code 722012 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3234-2018·2018-10-03
Philips Allura Xper F020 DR Table Recall for Monitor Suspension Defect
Philips is recalling 5,115 Allura Xper F020 DR Tables because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper F020 DR Table, System Code 722015 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19003·2018-10-03
Walmart Recalls Ozark Trail Camp Axes Due to Injury Hazard
Walmart is recalling Ozark Trail camp axes because the axe head can detach from the handle, posing an injury hazard.
Product
Ozark Trail camp axes
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18V691000·2018-10-03
Spartan Emergency Vehicles Recalled for Loose EMS Cabinet Fasteners
Spartan Motors is recalling 2001-2019 MetroStar and Gladiator emergency vehicles because EMS cabinet fasteners may be the wrong size, posing a crash injury risk.
Product
SPARTAN — SPARTAN METROSTAR, GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3219-2018·2018-10-03
Philips INTEGRIS Allura 9 F FDXD Monitor Suspension Recall
Philips is recalling INTEGRIS Allura 9 F FDXD systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
INTEGRIS Allura 9 F FDXD, System Code 722497 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3224-2018·2018-10-03
Philips Allura Xper FD2O Biplane Recall for Monitor Suspension Detachment Risk
Philips is recalling 5,115 Allura Xper FD2O Biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
Allura Xper FD2O Biplane, System Code 722008 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3216-2018·2018-10-03
Philips INTEGRIS Allura Monitor Ceiling Suspension Recall for Detachment Risk
Philips is recalling INTEGRIS Allura 15-12 systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Product
INTEGRIS Allura 15-12 (mono), System Code 722043 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1213-2018·2018-10-03
Hetero Recalls Montelukast Sodium Tablets Due to Blue Specks
Hetero Labs Limited is recalling 98,016 bottles of Montelukast Sodium 10 mg tablets because a pharmacist reported blue specks on the tablets.
Product
MONTELUKAST SODIUM — MONTELUKAST SODIUM (MONTELUKAST SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3250-2018·2018-10-03
Zimmer Biomet Recalls Vanguard 360 Knee Augments Due to Missing Bolt
Zimmer Biomet is recalling 16 Vanguard 360 Revision Knee System tibial block augments because the sterile packages contained one bolt instead of the required two.
Product
Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in Total Knee Arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1215-2018·2018-10-03
Baxter Recalls Levofloxacin Injection Bags Due to High Potency
Baxter Healthcare is recalling 523,896 bags of Levofloxacin Injection in 5% Dextrose because the drug concentration was higher than specified.
Product
LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3244-2018·2018-10-03
Tosoh G8 Automated HPLC Analyzer Recalled for Missing 510(k) Software
Tosoh Bioscience Inc is recalling eight G8 Automated HPLC Analyzers because they were distributed with software that lacks a 510(k).
Product
G8 Automated HPLC Analyzer - 723G8 Product Usage - In vitro diagnostic use for the quantitative measurement of % hemoglobin A1c in whole blood specimens. This test is to be used as an aid in the diagnosis of diabetes and as an aid in identifying patients who may be at risk…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1207-2018·2018-10-03
Noven Recalls Minivelle Estradiol Patches Due to Adhesive Defect
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.
Product
MINIVELLE — MINIVELLE (ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1210-2018·2018-10-03
Noven Recalls Minivelle Estradiol Patches Due to Adhesive Defects
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.
Product
MINIVELLE — MINIVELLE (ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3249-2018·2018-10-03
Zimmer Biomet Recalls Vanguard 360 Knee Augments Due to Missing Bolt
Zimmer Biomet is recalling 16 Vanguard 360 Revision Knee System tibial block augments because the sterile packages contained only one bolt instead of the required two.
Product
Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment, Model Number 185221 Intended for use in Total Knee Arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1208-2018·2018-10-03
Noven Recalls Minivelle Estradiol Patches Due to Adhesive Defect
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.
Product
MINIVELLE — MINIVELLE (ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Food)·F-1988-2018·2018-10-03
Caffeine-Free Barq's Root Beer Recalled for Mislabeling
Swire Coca Cola USA is recalling Caffeine-Free Barq's Root Beer 12 Packs due to mislabeling. The recall covers 2,945 cases distributed nationwide.
Product
Caffeine-Free Barq s Root Beer 12 Pack, 12 oz cans
Category
Food
Distribution
Distributed nationwide
HighNHTSA·18V687000·2018-10-02
Entegra Recalls 2019 Motorhomes Due to Park Brake Defect
Entegra is recalling 2019 Aspire, Anthem, and Insignia motorhomes because the park brake may fail to hold the vehicle on a grade.
Product
ENTEGRA — ENTEGRA INSIGNIA, ASPIRE, ANTHEM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V689000·2018-10-02
Jayco Recalls 2019 Precept Motorhomes Due to Wheel Stud Defect
Jayco is recalling 2019 Precept and Precept Prestige motorhomes because improperly heat-treated front wheel studs may break, increasing crash risk.
Product
JAYCO — JAYCO PRECEPT, PRECEPT PRESTIGE
Category
Vehicle
Distribution
Distributed nationwide