The Recall Desk

State

US Virgin Islands product recalls

73,388 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
2026-09-23

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.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21601–21625 of 73565

  • HighNHTSA·22V127000·2022-03-04

    2022 Kia Sorento Vehicles Recalled for Seatbelt Pretensioner Defect

    Kia is recalling 2022 Sorento Hybrid and Sorento PHEV vehicles because the front seatbelt pretensioner(s) may explode during a crash, potentially projecting metal fragments at occupants. Dealers will replace the pretensioners at no cost.

    Product
    KIA — KIA SORENTO PHEV, SORENTO HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V128000·2022-03-04

    Hino Recalls 2022 NJ7A Trucks Due to Air Brake Fastener Issue

    Hino is recalling 2022 NJ7A vehicles because an improperly tightened air compressor nut may cause low air pressure, potentially triggering the parking brake and increasing crash risk.

    Product
    HINO — HINO NJ7A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V123000·2022-03-03

    2022 Hyundai Elantra and Elantra HEV Seat Belt Pretensioner Explosion Hazard

    Hyundai is recalling 2022 Elantra and Elantra HEV vehicles because the front passenger-side seat belt pretensioner may explode during a crash, projecting metal fragments that could strike and injure vehicle occupants.

    Product
    HYUNDAI — HYUNDAI ELANTRA, ELANTRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V121000·2022-03-03

    Motorhome tire valve stem may lose pressure, increasing crash risk

    Jayco and Entegra motorhomes from 2018–2023 may have defective tire valve stem extensions that contact the wheel rim, causing damage and potential tire pressure loss that increases crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO ACCOLADE, ACCOLADE XL, SENECA PRESTIGE, SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E016000·2022-03-03

    Pony.ai Recalls Automated Driving Systems Due to Software Shutdown Risk

    Pony.ai is recalling specific Automated Driving Systems (ADS) because a software error may cause the system to shut down unexpectedly while the vehicle is moving.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V122000·2022-03-03

    Kawasaki Recalls W800 Motorcycles Due to Horn Harness Defect

    Kawasaki is recalling 2019-2022 W800 motorcycles because the horn harness may break, rendering the horn inoperable and increasing crash risk.

    Product
    KAWASAKI — KAWASAKI W800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22732·2022-03-03

    Ski-Doo Snowmobiles Recalled Due to Fire Hazard

    About 700 Ski-Doo snowmobiles from 2020–2022 are recalled because fuel can leak from the tank vent onto hot components when tilted or flipped, posing a fire hazard. BRP has received five reports of fires but no injuries.

    Product
    Ski-Doo Snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22089·2022-03-02

    Fitbit Recalls Ionic Smartwatches Due to Burn Hazard

    Fitbit is recalling about 1 million Ionic smartwatches sold in the U.S. because the lithium-ion battery can overheat and cause burns. At least 115 reports of battery overheating have been received, including 78 burn injuries.

    Product
    Fitbit Ionic smartwatches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V119000·2022-03-02

    BMW Recalls Multiple Models Due to PCV Valve Fire Risk

    BMW is recalling specific 2006-2013 models because a short circuit in the PCV valve heater could cause a fire while driving or when parked.

    Product
    BMW — BMW Z4, 3 SERIES, 5 SERIES, X5 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V118000·2022-03-02

    Freightliner M2 Brake Drum Defect May Cause Loss of Brake Function

    Daimler Trucks is recalling certain 2020-2022 Freightliner M2 trucks due to brake drum cracking that can cause brake failure and increase crash risk. All vehicles have been remedied.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0645-2022·2022-03-02

    RISE UP RED EDITION Capsules recalled for undeclared tadalafil

    RISE UP RED EDITION Capsules, 650 mg, have been recalled because they contain undeclared tadalafil, an ingredient found in FDA-approved male sexual enhancement products. The product is an unapproved drug and was distributed nationwide via Amazon Marketplace.

    Product
    RISE UP RED EDITION Capsules, 650 mg, 10-count blisters packaged in a carton, ASIN B08JCWG84D, barcode X002NI8PE1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0672-2022·2022-03-02

    Biomet Shoulder Implant Stem Recalled for Inadequate Coating Adhesion

    Biomet is recalling a Comprehensive Shoulder System implant component due to a defect in the porous plasma coating. The coating may not have sufficient adhesion strength, compromising the implant's structural integrity.

    Product
    Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 14 MM, 55 MM Long Item Number: 113614
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0665-2022·2022-03-02

    BD Vacutainer Luer Lok Access Device may shed particles causing false test results

    BD's Vacutainer Luer Lok Access Device may release contaminant particles that can be misidentified as red blood cells in laboratory analysis, potentially leading to false elevated RBC counts.

    Product
    BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port equipped with a threaded female luer during blood or urine sample collection using evacuated BD Vacutainer Blood or Urine Collection Tubes Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0670-2022·2022-03-02

    Hip implant revision system recalled due to inadequate coating adhesion

    Biomet is recalling 19 units of the Arcos Modular Revision Hip System because an incorrect rework process may have weakened the coating's adhesion strength, posing a potential implant failure risk.

    Product
    Arcos Modular Revision Hip System, Standard Cone Prox Body, Porous Plasma,Size A, 60 MM Item Number: 11-301301
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0658-2022·2022-03-02

    NobelReplace dental implant components recalled for driver engagement defect

    Nobel Biocare is recalling 702 NobelReplace dental implant components due to a manufacturing defect that prevents proper driver engagement. The defect could result in aborted or delayed surgical procedures.

    Product
    NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22091·2022-03-02

    Petzl PIRANA Descender Canyoneering Devices Recalled for Drowning Risk

    Petzl is recalling about 3,450 PIRANA descender canyoneering devices because the rope can get caught in the blocking slot, stopping or suspending the climber and creating a drowning risk under waterfalls or pools.

    Product
    PIRANA descender canyoneering devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0669-2022·2022-03-02

    RESODURA Matrix Onlay Recalled Due to Unsealed Packaging

    Collagen Matrix is recalling RESODURA matrix onlay dural substitutes due to outer packaging that is not properly sealed, potentially compromising sterility and creating a risk of infection.

    Product
    RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated as dural substitutes for the repair of dura matter. REF: DUMO10125
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0676-2022·2022-03-02

    Biomet Shoulder Implant Stem Recalled for Coating Adhesion Defect

    Biomet recalls 9 Comprehensive Shoulder System Mini Humeral Stems due to potential coating adhesion defects. An incorrect rework process may have compromised the porous plasma coating adhesion strength.

    Product
    Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 13 MM, 83 MM Long Item Number: 113633
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0671-2022·2022-03-02

    Shoulder Implant Stem Coating Defect Due to Invalid Rework Process

    Biomet is recalling a shoulder implant stem due to a manufacturing defect in the porous plasma coating. Internal testing indicated the coating may not have sufficient adhesion strength after an unvalidated waterjet rework process.

    Product
    Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 11 MM, 55 MM Long Item Number: 113611
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0661-2022·2022-03-02

    Video Camera Ceiling Tile Kits May Fall in Some Installations

    Natus Neurology is recalling IPELA FHD PTZ tile kits that may not fit properly in thinner ceiling tile grids and could suddenly fall, creating a safety hazard.

    Product
    IPELA FHD PTZ TILE KITS with Axis cameras used in combination with Natus Neuroworks/Sleepworks software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0677-2022·2022-03-02

    Shoulder Implant Stem Recalled for Defective Coating Adhesion

    Biomet is recalling Comprehensive Shoulder System Mini Humeral Stems due to defective porous plasma coating adhesion. Internal testing indicated affected parts may lack sufficient coating strength.

    Product
    Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 15 MM, 83 MM Long Item Number: 113635
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0668-2022·2022-03-02

    Collagen Dura Substitute Membrane Recalled for Compromised Sterility

    Collagen Matrix is recalling 68 units of DuraMatrix-Onlay Collagen Dura Substitute Membrane due to unsealed outer packaging that may compromise product sterility and increase infection risk.

    Product
    DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CDSLM45
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0673-2022·2022-03-02

    Biomet Shoulder Stem Implants Recalled for Coating Adhesion Defect

    Biomet is recalling certain shoulder stem implants due to potential insufficient adhesion strength in the porous plasma coating. An improper rework process may have compromised the coating's integrity.

    Product
    Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 18 MM, 55 MM Long Item Number: 113618
    Category
    Medical Device
    Distribution
    Distributed nationwide