The Recall Desk

State

US Virgin Islands product recalls

73,509 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
39
Most recent
2026-10-14

Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25726–25750 of 73686

  • HighFDA (Devices)·Z-1137-2021·2021-03-03

    Respironics Recalls 94 Philips Ventilator Batteries Due to Design Verification Issues

    Respironics is recalling 94 Philips V60 ventilator batteries because they were shipped without proper design verification. The recall covers distribution across multiple U.S. states.

    Product
    PHILIPS BATTERY, V60 14.4V, 11.0 Ah, 163 Wh, REF 1076374(1058272), LOT M94663-P1 - Product Usage: The ventilator is intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1145-2021·2021-03-03

    Smiths Medical Recalls Bivona Cuffless FlexTend Tracheostomy Tubes Due to Packaging Error

    Smiths Medical is recalling specific lots of Bivona Cuffless FlexTend Tracheostomy Tubes because they may have been packaged with the wrong neck flange, posing a risk of patient injury.

    Product
    Tube Tracheostomy and Tube Cuff, Bivona¿ Cuffless Neonatal/Pediatric FlexTend" Tracheostomy Tube (model 60PFS45, lots 3991171, 3991172, and 3988103) V Neck Flange 4.5mm - Product Usage: intended to provide direct airway access for a tracheotomized patient for up to 29 days. It…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1142-2021·2021-03-03

    Recall of Parietex Hydrophilic Anatomical Mesh Due to Incorrect Side Labeling

    Covidien is recalling Parietex hydrophilic anatomical mesh where the package label indicates left-side use but contains a right-side device. This labeling error can lead to implant failure and hernia recurrence.

    Product
    Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm polyester left - Product Usage: designed for the repair of inguinal hernias via laparoscopic or posterior open procedures Item Code: TECT1510AL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V132000·2021-03-03

    2021 Volkswagen Atlas Wheels May Separate Due to Machining Defect

    Volkswagen is recalling certain 2021 Atlas and Atlas Cross Sport vehicles due to improperly machined wheel lug bolt holes that may prevent wheels from attaching properly, risking wheel separation and crashes.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1148-2021·2021-03-03

    Northgate Recalls Steris CO2MPACT Endoscopic Insufflator Systems Due to Tubing Material Error

    Northgate Technologies is recalling 45 Steris CO2MPACT Endoscopic Insufflator systems because an internal tubing component was made with incorrect, untested material.

    Product
    Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: designed to use CO2 as a distention media in the gastrointestinal tract when used in conjunction with a gastrointestinal endoscope.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1141-2021·2021-03-03

    Ecolab Recalls Slush and Warmer Disc Drapes Due to Sterile Barrier Risk

    Ecolab is recalling specific lots of ORS-320 Slush + Warmer Disc Drapes because manufacturing slits may breach the sterile barrier, posing an infection risk to patients.

    Product
    Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product Usage: single-use equipment cover intended for use during various surgeries where warm irrigation, slush and/or cold solution is required.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0287-2021·2021-03-03

    Dr. Reddy's Recalls Imatinib Mesylate Tablets for Dissolution Failures

    Dr. Reddy's Laboratories is recalling specific lots of Imatinib Mesylate 100mg tablets because they failed to meet required dissolution specifications.

    Product
    IMATINIB — IMATINIB (IMATINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0270-2021·2021-03-03

    Areva Pharmaceuticals Recalls Irinotecan Hydrochloride Injection Due to CGMP Deviations

    Areva Pharmaceuticals is recalling 3,287 vials of Irinotecan Hydrochloride Injection due to manufacturing quality deviations identified in a Warning Letter.

    Product
    Irinotecan Hydrochloride Injection, USP, 40 mg/2 mL (20 mg/mL), 2 mL Single-Dose Vial, Rx Only, Distributed by: Areva Pharmaceuticals, Inc., Gerogetown, IN 47122, Made in India, NDC 59923-714-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1144-2021·2021-03-03

    Siemens ARTIS Icono Biplane and Floor Systems Recalled for Software Errors

    Siemens is recalling 41 ARTIS Icono systems with software version VE20B due to misleading error messages and manual gaps that may cause procedure termination.

    Product
    ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700 with software version VE20B - Product Usage: Intended for single and biplane diagnostic imaging and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1135-2021·2021-03-03

    Medline Recalls STAT-Site B-HB Controls Due to Shipment Compromise

    Medline Industries is recalling specific lots of STAT-Site B-HB controls because the products were compromised during shipment. The recall affects 46 units distributed in Mississippi, Ohio, and Illinois.

    Product
    S-O303000 CONTROL, STAT-SITE B-HB, 2X3ML,1LOW,1HIGH - Product Usage: intended for the quantitative determination of the ketone body ¿-Hydroxybutyrate in serum or plasma. For laboratory use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V130000·2021-03-02

    Ferrara Recalls 2009-2020 Aerial Vehicles Due to Trolley Defect

    Ferrara is recalling 2009-2020 Aerial vehicles because a defective waterway trolley can detach and fall, posing a risk of injury or death.

    Product
    FERRARA — FERRARA AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V127000·2021-03-01

    Hyundai Recalls Kona and Ioniq Electric Vehicles for Battery Fire Risk

    Hyundai is recalling 2019-2020 Kona Electric and 2020 Ioniq Electric vehicles because the lithium-ion battery may short-circuit, increasing the risk of a fire.

    Product
    HYUNDAI — HYUNDAI KONA ELECTRIC, IONIQ ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·008-2021·2021-03-01

    Milky Way Recalls Canned Corned Beef Imported Without Inspection

    Milky Way International Trading Corp. is recalling approximately 297,715 pounds of canned corned beef products that were imported and distributed in the U.S. without FSIS import re-inspection.

    Product
    Milky Way International Trading Corp. Recalls Canned Corned Beef Products Imported Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V122000·2021-02-26

    KTM Recalls 2020 1290 Super Duke R Motorcycles for Wiring Harness Defect

    KTM is recalling 2020 1290 Super Duke R motorcycles because an incorrectly routed rear wiring harness could cause an electrical short-circuit, leading to engine stalling and increased crash risk.

    Product
    KTM — KTM 1290 SUPER DUKE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V123000·2021-02-26

    Mercedes-Benz Recalls 2018 GLE Models Due to Tire Defect

    Mercedes-Benz is recalling 2,529 2018 GLE 350, GLE 400, and AMG GLE43 vehicles because over-cured tires may fail, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 400, AMG GLE43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V115000·2021-02-25

    GM Recalls 33,838 Vehicles Due to Over-Cured Continental Tires

    General Motors is recalling 33,838 vehicles equipped with over-cured Continental tires that may develop sidewall breaks or belt separation, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC EXPRESS, SIERRA 1500, SAVANA, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V119000·2021-02-25

    Vermeer Recalls 2021 BC900XL Trailers Due to Axle Bolt Issue

    Vermeer is recalling 2021 BC900XL brush chipper trailers because axle mounting bolts may not be tightened properly, increasing crash risk.

    Product
    VERMEER — VERMEER BC900XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V120000·2021-02-25

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Engine Software Defect

    Daimler Trucks North America is recalling 2019-2021 Thomas Built Buses Saf-T-Liner C2 school buses because engine software may fail to limit speed or torque, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V118000·2021-02-25

    Jaguar Recalls 2019-2020 F-Pace for High Beam Indicator Software Defect

    Jaguar is recalling 2019-2020 F-Pace vehicles because the Auto High Beam system fails to display an indicator when high beams activate, potentially reducing visibility for oncoming traffic.

    Product
    JAGUAR — JAGUAR F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide