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.

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.

25126–25150 of 73686

  • HighNHTSA·21V314000·2021-05-04

    Arcimoto Motorcycles Recalled for Defective Seat Belt Retractors

    Arcimoto is recalling certain 2019-2021 motorcycles because the seat belt retractor spool sleeve may crack, preventing the belt from retracting. This increases the risk of injury. Owners should contact Arcimoto for free replacement.

    Product
    ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V311000·2021-05-04

    Arcimoto Electric Vehicles Recalled: Inverter Software Error Causes Battery Shutdown Risk

    Arcimoto is recalling 2019-2021 FUV, 2020 Deliverator, 2020-2021 Roadster, and 2021 Rapid Responder vehicles due to a software error that may cause unexpected battery shutdown, increasing crash risk. Owners should contact Arcimoto or NHTSA for remedy details.

    Product
    ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER, ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V312000·2021-05-04

    Blue Bird Recalls 2018-2022 All American Buses Due to Fuel Leak Risk

    Blue Bird is recalling 2018-2022 All American buses because a fuel rail leak could cause a fire. Owners should contact customer service for updates.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V310000·2021-05-04

    2021 Jeep Cherokee Transmission Oil Cooler Hose May Leak and Cause Fire

    Chrysler is recalling certain 2021 Jeep Cherokee vehicles because the transmission oil cooler hose may have been incorrectly cured, allowing transmission fluid to leak and increasing the risk of fire. Dealers will inspect and replace the hose for free.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V308000·2021-05-03

    2021 Hyundai Santa Fe Fuel Pipe Connection Defect Recall

    Hyundai is recalling 2021 Santa Fe vehicles with 2.5-litre Turbo engines due to improperly tightened fuel pipe connections that may leak fuel and increase fire risk. The affected vehicles have already been repaired at dealerships at no cost to owners.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V307000·2021-05-03

    Arcimoto Electric Motorcycles Recalled for Steering Angle Sensor Failure

    Arcimoto is recalling multiple 2019-2021 motorcycle models due to faulty steering angle sensors that may cause oversteer and increase crash risk. The company will update firmware and replace the idler arm at no cost.

    Product
    ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER, ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E038000·2021-04-30

    Mando Recalls ABS Modules Due to Electrical Short Circuit Fire Risk

    Mando America Corporation is recalling specific Anti-lock Brake System (ABS) modules that may malfunction and short circuit, increasing the risk of an engine compartment fire.

    Product
    SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E039000·2021-04-30

    Mando Recalls ABS Modules for Brake Fluid Leak and Fire Risk

    Mando America Corporation is recalling certain Anti-lock Brake System (ABS) modules that may leak brake fluid and cause a short circuit, increasing the risk of an engine compartment fire.

    Product
    SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V304000·2021-04-30

    KTM Recalls 790 Adventure Motorcycles Due to Weak Front Brake Spring

    KTM is recalling 2019-2020 790 Adventure models because a weak front brake spring may reduce braking functionality, increasing the risk of a crash.

    Product
    KTM — KTM 790 ADVENTURE, 790 ADVENTURE R, 790 ADVENTURE R RALLY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V306000·2021-04-30

    Tiffin Bus and Phaeton motorhomes recalled for fuel rail leakage and fire risk

    Tiffin Motorhomes is recalling 2017-2021 Bus and Phaeton vehicles due to fuel rail assembly defects that may leak, posing a fire risk. Owners should contact Tiffin customer service at 1-256-356-8661 for a free inspection.

    Product
    TIFFIN — TIFFIN BUS, PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V305000·2021-04-30

    NorthStar Ambulance Recall for Display Lockup Hazard

    Braun Northwest is recalling 2013-2020 NorthStar Ambulances because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    NORTHSTAR — NORTHSTAR AMBULANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21740·2021-04-29

    Modernist Pantry Recalls Sodium Hydroxide for Packaging and Labeling Defects

    Modernist Pantry is recalling Kitchen Alchemy Sodium Hydroxide products because the packaging is not child-resistant and labels violate federal hazardous substance requirements.

    Product
    Modernist Pantry Kitchen Alchemy Sodium Hydroxide
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21E037000·2021-04-29

    Full Vision Recalls Rogers Brothers Rear Impact Guards Due to Weak Steel

    Full Vision is recalling Rogers Brothers Rear Impact Guards because the steel may not meet specifications, potentially reducing strength and increasing injury risk in crashes.

    Product
    STRUCTURE:BODY:BUMPERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0481-2021·2021-04-28

    Real Alkalized Water Recalled Due to Acute Liver Failure Reports

    Real Water, Inc. is recalling Real Alkalized Water in various bottle sizes after the FDA was notified of cases of acute liver failure following consumption.

    Product
    Real Alkalized Water, packed in 16.9 oz., 1 Liter, 1.5 Liter, 1-Gallon and 5-Gallon plastic bottles. Drinkrealwater.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0482-2021·2021-04-28

    Real Alkalized Water Concentrate Recalled Due to Liver Failure Reports

    Real Water, Inc. is recalling Real Alkalized Water concentrate after FDA was notified of cases of acute liver failure following consumption.

    Product
    Real Alkalized Water, concentrate. 4 oz. glass bottle . Drinkrealwater.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1476-2021·2021-04-28

    Smiths Medical Recalls Manifold Rotators Due to Incomplete Welds

    Smiths Medical ASD Inc. is recalling specific lots of manifold rotators and related components because they may have insufficient or incomplete welds.

    Product
    Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR, OFF HANDLE, Model Number MX1232MR b. 250 3 GANG MANIFOLD ROTATOR, OFF HANDLE, Model Number MX1233MR c. 550 2 GANG MANIFOLD ROTATOR, OPEN HANDLE, Model Number MX1322MR d. 550 3 GANG MANIFOLD ROTATOR, OFF HANDLE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1467-2021·2021-04-28

    AngioDynamics Safe Sheath Ultralite Recalled for Potential Sterility Compromise

    AngioDynamics is recalling specific Safe Sheath Ultralite kits due to potential sterility compromise. The recall affects 337 units distributed nationwide.

    Product
    AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter Introducer Catalogue #: VI10 - Product Usage: For the introduction of various types of pacing leads and catheters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1479-2021·2021-04-28

    Smiths Medical Recalls High Pressure Rotators Due to Incomplete Welds

    Smiths Medical ASD Inc. is recalling specific lots of Medex High Pressure Rotators because they may have insufficient or incomplete welds.

    Product
    HIGH PRESSURE ROTATOR (Component) a. WITH MALE LUER LOCK, Model Number MX496HP b. WITH FEMALE LUER LOCK, Model Number MX497HP. component of extravascular blood-pressure Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1426-2021·2021-04-28

    HeartWare HVAD System Manual Updates for Carrying Cases and Driveline Cover

    Heartware, Inc. is updating the Instructions for Use and Patient Manual for the HVAD System to clarify carrying case care, driveline cover orientation, and controller power-up sequences.

    Product
    Instructions for Use and Patient Manual for HeartWare HVAD System. Accompanies these system components: HVAD Sterile Implant Kit, Model Numbers: 1100, 1101, 1102, 1103, 1104, 1104JP, 1205, MCS1705PU HVAD Controller Kit, Model Numbers: 1403US, 1407AU, 1407CA, 1407CH, 1407DE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1481-2021·2021-04-28

    Smiths Medical Recalls Medex Pressure Injector Lines Due to Weld Defects

    Smiths Medical ASD Inc. is recalling specific lots of Medex pressure injector lines and related components due to insufficient or incomplete welds.

    Product
    Medex 10 IN Pressure Injector Line w/Rot (1200psi) NS. REF B1681R, component of extravascular blood-pressure Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1445-2021·2021-04-28

    BIOTRONIK Ilestro 7 VR-T DX Defibrillators Recalled for Battery Depletion

    BIOTRONIK Inc is recalling 3,664 Ilestro 7 VR-T DX implantable defibrillators due to a potential for premature battery depletion.

    Product
    BIOTRONIK Ilestro 7 VR-T DX, DF-1, REF 383594, UDI: 04035479125509 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1437-2021·2021-04-28

    Stryker Recalls Tritanium X TL Spinal Instruments Due to Failure Risk

    Stryker Spine is recalling 169 sets of Tritanium X TL instruments because non-conforming components could lead to device failure during surgery.

    Product
    Tritanium X TL Instruments - intervertebral fusion device with bone graft, lumbar. Catalogs:TL Inserter (580220100), TL Draw Rod (580220101), Tube Set/Syringe Adapter Assembly (680220100), Syringe Plunger (680220102).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1459-2021·2021-04-28

    Biotronik Inventa 7 ICDs Recalled for Premature Battery Depletion

    Biotronik is recalling Inventa 7 ICDs and CRT-Ds due to a potential for premature battery depletion. The recall covers devices distributed nationwide and worldwide.

    Product
    BIOTRONIK INVENTRA 7, VR-T DX DF-1 ProMRI, REF 399436, UDI: 04035479136314 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1375-2021·2021-04-28

    Aftermarket Alaris Infusion Pump Front Bezel Recall for Potential Infusion Errors

    Pacific Medical Group is recalling 2,452 aftermarket Alaris infusion pump front bezels installed between July 2020 and February 2021. The bezel posts may crack or separate, potentially causing infusion errors.

    Product
    Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel, installed by Pacific Medical Group (DBA Avante Health Solutions)
    Category
    Medical Device
    Distribution
    Distributed nationwide