The Recall Desk

State

US Virgin Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33076–33100 of 73900

  • ModerateFDA (Devices)·Z-1955-2019·2019-07-17

    MAHURKAR and Argyle acute hemodialysis catheters recalled for inaccurate priming volume labels

    COVIDIEN LLC is recalling MAHURKAR and Argyle acute hemodialysis catheters because the printed priming volume values are higher than the volumes required to fill each lumen.

    Product
    MAHURKAR and Argyle acute hemodialysis catheters, Material numbers 8813793009 8813793013 8813794005 8813794009 8813816005 8813816009 8813817005 8813817009 8815668007 8815668011 8815668021 8815668027 8817142005 8817143005 8817145005 8817146001 8817146007…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1958-2019·2019-07-17

    Canon Radrex-i X-Ray System Software Malfunction Recall

    Canon Medical System is recalling 46 Radrex-i X-Ray Systems due to a software malfunction that prevents image transmission from the wireless flat panel detector.

    Product
    Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software version: v5.00ER005 Product Usage: The RADREX-I is a general purpose x-ray system that employs Solid State Imager(s), SSXI, which converts x-rays directly into electrical signals which can, after…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1957-2019·2019-07-17

    Richard Wolf Recalls E-Line Cutting Electrode Due to Incorrect Product Packaging

    Richard Wolf Medical Instruments Corp. is recalling E-Line Cutting Electrodes because some packages contain the wrong electrode type.

    Product
    E-Line Cutting Electrode 11.5Fr Mono 0 degrees, Sterile. One electrode is placed in a plastic tray and then inserted into a Tyvek pouch. Five packaged electrodes are placed in a white box. Product Usage: Resectoscopes are used for endoscopically controlled ablation of tissue.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1952-2019·2019-07-17

    Rinovum Recalls Revive Reusable Bladder Support Due to Structural Defect

    Rinovum Women's Health is recalling the Revive Reusable Bladder Support because the device may split or crack during its intended use life.

    Product
    Revive Reusable Bladder Support, Model No. 0025 - Product Usage: The Revive bladder support is intended for temporary management of urinary leakage caused by stress urinary incontinence (SUI) in women, 18 years and older. The device comes in a sealed box, and contains a reusable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19168·2019-07-16

    K2 Sports Recalls VO2 S Inline Skates Due to Fall Hazard

    K2 Sports is recalling VO2 S inline skates because the axle can loosen or break, causing wheels to separate and posing a fall hazard. No injuries have been reported.

    Product
    VO2 S inline skates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19167·2019-07-16

    VIVO Recalls Speaker Wall Mounts Due to Fall and Injury Hazards

    VIVO is recalling MOUNT-PLAY5 speaker wall mounts because the front ledge can loosen, causing speakers to fall. No injuries have been reported.

    Product
    VIVO MOUNT-PLAY5 speaker wall mounts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19762·2019-07-16

    Majestic Pure Wintergreen Oil Recalled for Non-Child-Resistant Packaging

    Epic Business Services is recalling Majestic Pure Wintergreen Oil because the packaging fails to meet child-resistant closure requirements, posing a poisoning risk to young children.

    Product
    Majestic Pure Wintergreen Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V530000·2019-07-14

    BYD Recalls 2019 C8M Buses Due to Glass Roof Hatch Shattering Risk

    BYD is recalling 2019 C8M buses because temperature and vibration stresses may cause the tempered glass roof escape hatches to shatter, potentially injuring passengers.

    Product
    BYD — BYD C8M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V526000·2019-07-12

    Blue Bird Recalls School Buses Due to Roof Hatch Handle Defect

    Blue Bird is recalling 2018-2020 Vision and All American school buses because the roof emergency exit handle may break, preventing easy opening during an emergency.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V523000·2019-07-12

    Spartan Gladiator and MetroStar Front Shock Separation Recall

    Spartan is recalling 2014-2020 Gladiator and MetroStar vehicles because front shocks may separate, potentially causing a loss of power steering assist and increasing crash risk.

    Product
    SPARTAN — SPARTAN GLADIATOR, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V529000·2019-07-12

    American Coach Motorhomes Recalled for Rear Air Deflector Detachment Risk

    REV Recreation Group is recalling 2016-2019 American Coach motorhomes because rear air deflectors may detach, creating a road hazard.

    Product
    AMERICAN COACH — AMERICAN COACH AMERICAN HERITAGE, AMERICAN EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V525000·2019-07-12

    Heartland Recalls Fifth-Wheel Trailers Due to A/C Electrical Connector Fire Risk

    Heartland is recalling specific 2016-2020 fifth-wheel trailers because an improperly installed A/C electrical connector may overheat and increase the risk of a fire.

    Product
    HEARTLAND — HEARTLAND PIONEER, NORTH PEAK, MILESTONE, ELKRIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V524000·2019-07-12

    Blue Bird Recalls 2020 School Buses for Roof Hatch Handle Defect

    Blue Bird is recalling 2020 Vision and All American school buses because the roof hatch handle may break, preventing emergency exit.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V528000·2019-07-12

    KME Fire Trucks Recalled for Cab Hydraulic Velocity Fuse Defect

    KME is recalling various 2016-2020 Predator and Predator Panther fire trucks because hydraulic velocity fuses may fail to lock the cab during a system failure, posing an injury risk to occupants.

    Product
    KME — KME PREDATOR PANTHER PUMPER, PREDATOR SS PUMPER, PREDATOR SS RESCUE, PREDATOR AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19164·2019-07-11

    Lidl Recalls Wooden Grasping Toys Due to Choking Hazard

    Lidl is recalling Playtive Junior Wooden Grasping Toys because the wheels can detach, posing a choking hazard to young children.

    Product
    Playtive Junior Wooden Grasping Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19761·2019-07-11

    Levolor Recalls Custom Cellular Shades Due to Strangulation Hazard

    Levolor is recalling about 30,000 custom cellular shades because the pull cords are joined by a non-breakaway connector, posing a strangulation hazard to small children.

    Product
    Levolor Two-Corded Custom Cellular Shades
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19165·2019-07-11

    Lifetime Brands Recalls Fitz and Floyd Can Mugs Due to Burn Hazards

    Lifetime Brands is recalling Fitz and Floyd Nevaeh White can mugs because they can crack or break when exposed to hot liquids, posing burn and laceration hazards.

    Product
    Fitz and Floyd® Nevaeh White® Can Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V520000·2019-07-11

    Micro Bird Recalls 2019 MB II Buses Due to Fire Risk

    Micro Bird is recalling 52 model-year 2019 MB II propane-powered buses because a melted grounding wire could cause an engine compartment fire.

    Product
    MICRO BIRD — MICRO BIRD MB II TRANSIT BUS, MB II SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1488-2019·2019-07-10

    PharMEDium Recalls Hydromorphone Syringes Due to Sulfite Mislabeling

    PharMEDium Services is recalling 28,140 hydromorphone syringes because the product is labeled as sulfite-free but contains sulfites.

    Product
    Hydromorphone HCl in 0.9% sodium chloride, 0.5mg per mL, 1 mL in 3mL BD Syringe, PharMEDium 913 N Davis Ave Cleveland, MS 38732, 800-523-7749, NDC 61553-352-78
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1905-2019·2019-07-10

    Siemens Fluoroscopic X-Ray Systems Recalled for Potential Screw Failure

    Siemens is recalling eight Artis fluoroscopic X-ray systems because screws on the ceiling-mounted support may loosen or snap, posing a risk of severe injury.

    Product
    Siemens Artis pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1894-2019·2019-07-10

    Siemens Artis zee X-Ray Systems Recalled for Ceiling Support Screw Failure

    Siemens is recalling 63 Artis zee X-ray systems because ceiling support screws may loosen or snap, posing a risk of severe injury to patients and staff.

    Product
    Siemens Artis zee floor -Interventional Fluoroscopic X-Ray System Model Number: 10094135
    Category
    Medical Device
    Distribution
    Distributed nationwide