The Recall Desk

State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39101–39125 of 73919

  • ModerateFDA (Devices)·Z-1270-2018·2018-04-04

    Roche cobas e 411 Analyzer Recall for Questionable Results

    Roche Diagnostics is recalling cobas e 411 Immunoassay Analyzers because using 13 mm sample tubes without adapters may cause questionable results.

    Product
    cobas e 411 Immunoassay Analyzer (Discrete Photometric Analyzer for Clinical use), Catalog Numbers: 04775201001 (rack system), 04775279001 (disk system), 04775201973 (rack system) & 04775279973 (disk system).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2018·2018-04-04

    Zimmer Dental Recalls Tapered Screw-Vent Implants Due to Labeling Error

    Zimmer Dental Inc is recalling Tapered Screw-Vent MTX dental implants because two lots were inadvertently commingled during manufacturing, potentially resulting in mislabeling.

    Product
    Tapered Screw-Vent MTX, Dental Implant, sterile. Model TSVTB10.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1242-2018·2018-04-04

    Mindray Gas Module 3 monitoring spirometer recalled for regulatory changes

    Mindray DS USA is recalling 1,719 Gas Module 3 monitoring spirometers because the firm made multiple changes to the product requiring the submission of a new 510(k) premarket notification.

    Product
    Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device designed to monitor airway gases during anesthesia and/or assisted respiration. Monitored gases includes O2, CO2, N2O and anesthetic agents Halothane…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0613-2018·2018-04-04

    Akorn Recalls Subpotent Chlorhexidine Oral Rinse Kits

    Akorn, Inc. is recalling 24-HOUR Oral Care q4 Kits containing subpotent Chlorhexidine Gluconate Oral Rinse due to product crystallization.

    Product
    24-HOUR Oral Care q4 Kit with Ballard* Technology, containing 2 Toothbrush Packs with CHG Solution, Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cup (NDC 50383-720-15), Rx Only, Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701; Kit Manufactured by Halyard Health…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0605-2018·2018-04-04

    Renaissance Lakewood Recalls Flucanazole Injection Due to Stability Failures

    Renaissance Lakewood, LLC is recalling 1,277 bags of Flucanazole Injection due to superpotent and failed stability specifications.

    Product
    Flucanazole Injection, USP 200 mg in in 100 mL (2 mg/mL), 10 Single Dose Flexible Containers, Rx Only, Manufactured for: Claris Lifesciences, Inc. North Brunswick, NJ 08902 By; Claris Injectables Ltd. Gujarat, India --- NDC 36000-006-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V211000·2018-04-03

    Toyota Recalls 2017-2018 Models for Brake Booster Vacuum Pump Defect

    Toyota is recalling specific 2017-2018 Camry, Highlander, Sienna, Tacoma, and Lexus RX350 vehicles because a manufacturing defect in the brake booster vacuum pump may cause a sudden loss of brake assist.

    Product
    TOYOTA — TOYOTA, LEXUS SIENNA, TACOMA, RX350, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18135·2018-04-03

    3M Recalls Scotch Thermal Laminators Due to Overheating Burn Hazard

    3M is recalling about 395,000 Scotch thermal laminators because the plastic enclosure can overheat, posing a burn hazard. No injuries have been reported.

    Product
    Scotch™ thermal laminators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18133·2018-04-02

    Polaris Recalls RZR XP 1000 Vehicles Due to Exhaust Fire Hazard

    Polaris is recalling about 107,000 RZR XP 1000 vehicles because a cracked exhaust silencer can cause a fire. No injuries have been reported.

    Product
    Model Year 2014-2018 Polaris RZR XP 1000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V209000·2018-03-30

    Van Hool Recalls Motorcoaches Due to Seat Belt Buckle Casing Failure

    Van Hool is recalling 2015-2018 motorcoaches because seat belt buckle casings may fail, exposing the buckles and reducing the likelihood of seat belt use.

    Product
    VAN HOOL — VAN HOOL CX45, TD925, TDX25, CX35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V208000·2018-03-29

    Mercedes-Benz Recalls 2018 Models for Driver Air Bag Inflator Defect

    Mercedes-Benz is recalling 2018 AMG GT, AMG GT C, GLC43 AMG, GLC300, and GLC350e vehicles because defective steel in the driver-side air bag inflator housing may cause rupture during deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E, GLC 300, AMG GLC43, AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V203000·2018-03-29

    Alfa Romeo Stelvio Recall for Liftgate Wiring Water Leak

    FCA US LLC is recalling 2018 Alfa Romeo Stelvio vehicles because water leaks into liftgate wiring, causing corrosion that may allow the liftgate to open while driving.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V206000·2018-03-29

    Spartan Gladiator Recall for Front Axle Spindle Failure Risk

    Spartan Motors is recalling 2004-2007 Gladiator emergency response vehicles because front axle spindles may crack and fail, potentially causing a wheel to separate.

    Product
    SPARTAN — SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V199000·2018-03-29

    Navistar Recalls 2018-2019 International LT Trucks for Fuel Leak Risk

    Navistar is recalling 2018-2019 International LT trucks because a fender splash panel may rub against the fuel line, causing a leak that could lead to fire or crash.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E017000·2018-03-29

    Timoney Front Suspension Recall Due to Axle Spindle Fatigue Cracks

    Timoney Technology is recalling Mark 1 and Gen 2 Independent Front Suspensions because inconsistent machining may cause axle spindle failure and wheel separation.

    Product
    SUSPENSION:FRONT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V204000·2018-03-29

    Tesla Recalls Model S Vehicles Due to Steering Bolt Corrosion Risk

    Tesla is recalling 2012-2016 Model S vehicles because aluminum steering bolts may corrode and fracture, potentially causing a loss of power steering assist.

    Product
    TESLA — TESLA MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18733·2018-03-29

    Residential Elevators Recalls Traction Elevators Due to Impact Hazard

    Residential Elevators Inc. is recalling about 3,700 traction elevators installed in homes between January 2015 and April 2017 because the cab can rise unexpectedly to the top of the shaft, posing an impact hazard.

    Product
    Traction elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V207000·2018-03-29

    Mercedes-Benz Recalls 2017-2018 Models Due to Front Seatback Locking Defect

    Mercedes-Benz is recalling specific 2017-2018 C-Class and E-Class vehicles because front seatbacks may not lock properly, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 400, C 300, AMG C63S, AMG C43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V205000·2018-03-29

    Alfa Romeo Stelvio Recall for Water-Induced Electrical Corrosion

    FCA US LLC is recalling 2018 Alfa Romeo Stelvio vehicles because water leaks into the body control module, causing electrical malfunctions that increase crash risk.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18734·2018-03-29

    Octane Fitness Recalls XT-One Elliptical Cross Trainers Due to Fall Hazard

    Octane Fitness is recalling about 570 XT-One elliptical cross trainers because the incline lead screw can shear off, causing foot pedals to drop unexpectedly and creating a fall hazard.

    Product
    Octane Fitness XT-One elliptical cross trainers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18132·2018-03-29

    Primo Recalls hTrio Beverage Dispensers Due to Burn Hazard

    Primo is recalling hTrio beverage dispensers because hot water may leak at high altitudes, posing a burn risk.

    Product
    Primo hTrio Multi-purpose beverage dispensers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1122-2018·2018-03-28

    MedComp Recalls 12F Tesio Catheter Sets Due to Connection Failure Risk

    Medical Components, Inc. is recalling 385 12F Tesio Catheter Sets because connection failures may cause blood loss or air emboli.

    Product
    12F Tesio CATHETER SET (CUFF 22CM FROM TIP), REF MCTC1235SD, UDI 884908027242 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide