The Recall Desk

State

US Virgin Islands product recalls

72,992 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
30
Most recent
2026-09-09

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 30 (17%) are Severe.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9576–9600 of 73169

  • ModerateFDA (Devices)·Z-2960-2024·2024-09-11

    Impella CP Cardiac Assist Pump Lacks Shockwave Catheter Interaction Warning

    Abiomed is updating labeling for Impella CP Smart Assist pumps to address a potential interaction with Shockwave Coronary IVL Catheters during coronary interventions. The interaction was previously undocumented in device labeling.

    Product
    Impella CP Smart Assist Set APAC; Product Code: 0048-0047;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2954-2024·2024-09-11

    Impella CP Smart Assist Set: Device interaction safety labeling update

    Abiomed is updating labeling for the Impella CP Smart Assist Set to address a potential device interaction with the Shockwave Coronary IVL Catheter during coronary procedures. No illnesses or injuries have been reported.

    Product
    Impella CP Smart Assist Set, EU; Product Code: 0048-0014;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2969-2024·2024-09-11

    Impella CP Smart Assist Set: Potential Device Interaction with Coronary Catheter

    Abiomed is updating labeling for the Impella CP Smart Assist Set to address a potential device interaction with the Shockwave Coronary IVL Catheter during coronary procedures.

    Product
    Impella CP Smart Assist Set; Product Code: 1000402;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2961-2024·2024-09-11

    Impella 5.5 with SmartAssist Set: Potential Device Interaction During Coronary Interventions

    Abiomed is updating labeling for Impella 5.5 with SmartAssist Set due to a potential device interaction with Shockwave Coronary IVL Catheter during coronary interventions. The product labeling currently lacks information about this potential interaction.

    Product
    Impella 5.5 with SmartAssist Set, EU; Product Code: 0550-0002;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2962-2024·2024-09-11

    Impella 5.5 Cardiac Pump Labeling Updated for Device Interaction Risk

    Abiomed is updating documentation for the Impella 5.5 cardiac pump to address a potential device interaction with the Shockwave Coronary IVL Catheter during coronary procedures. The notice affects 21 units distributed worldwide.

    Product
    Impella 5.5 with SmartAssist Set, CA; Product Code: 0550-0004;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2967-2024·2024-09-11

    Impella CP Smart Assist Set Recalled for Device Interaction Labeling Update

    Abiomed is updating labeling for ImpellaCP SmartAssistSetAPAC to address a potential interaction with Shockwave Coronary IVL Catheters during coronary interventions. Eight units were distributed worldwide.

    Product
    ImpellaCP SmartAssistSetAPAC, Delo1895; Product Code: 1000302;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2959-2024·2024-09-11

    Abiomed Impella Pump Recall for Potential Shockwave Catheter Interaction

    Abiomed is recalling 43,636 Impella Pumps to update instructions for use regarding a potential interaction with Shockwave Coronary IVL Catheters.

    Product
    Pump 371 14F LT CMR Set; Product Code: 0048-0045;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2963-2024·2024-09-11

    Abiomed Impella 5.5 Recall for Potential Shockwave Catheter Interaction

    Abiomed is recalling 2,916 Impella 5.5 units to update labeling regarding a potential interaction with Shockwave Coronary IVL Catheters during coronary interventions.

    Product
    Impella 5.5 with SmartAssist Set, US; Product Code: 0550-0008;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2971-2024·2024-09-11

    Impella 5.5 Cardiac Pump Recalled for Undocumented Device Interaction

    Abiomed recalled 413 units of Impella 5.5 with SmartAssist S2 pumps worldwide due to a potential undocumented interaction with Shockwave coronary catheters during cardiac procedures. The company will update product labeling to disclose this interaction.

    Product
    Impella 5.5 with SmartAssist S2 Set, EU; Product Code: 1000482;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2953-2024·2024-09-11

    Philips Azurion 7M20 Fluoroscopic X-Ray System FlexArm Movement Recall

    Philips Azurion 7M20 interventional fluoroscopic X-ray systems with FlexArm ceiling-mounted stands may experience inconsistent or unavailable longitudinal movement due to bearing grease leakage affecting device mobility. Approximately 927 systems worldwide are affected.

    Product
    Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, Interventional Fluoroscopic X-Ray System, Model Numbers 722079 and 722224
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V666000·2024-09-10

    Thor Motor Coach Recalls 2024 Motorhomes Due to Overheating Propane Tank Risk

    Thor Motor Coach is recalling 2024 Palladium and Talavera motorhomes because the liquid propane tank is located too close to the chassis exhaust, creating a fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH PALLADIUM, TALAVERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V661000·2024-09-10

    McLaren Recalls 2020-2023 GT Models Due to Hood Latch Defect

    McLaren is recalling 2020-2023 GT vehicles because the hood latch cable may have excessive tension, causing the hood to open unexpectedly and obstruct the driver's view.

    Product
    MCLAREN — MCLAREN GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V663000·2024-09-10

    Alliance RV Valor travel trailers recalled for missing electrical shock protection

    Alliance RV is recalling certain 2024-2025 Valor travel trailers where the front bathroom outlet may lack Ground Fault Interrupter (GFI) protection. This missing safety feature can result in electrical shock.

    Product
    ALLIANCE RV — ALLIANCE RV VALOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V668000·2024-09-10

    Freightliner and Western Star brake lights may fail during emergency braking

    Daimler Trucks is recalling certain Freightliner and Western Star trucks because brake lights may fail to illuminate during automatic emergency braking, increasing crash risk. Dealers will update software at no cost.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 49X, 47X, 114SD, BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V659000·2024-09-09

    Mercedes-Benz G 550 rear door latch defect poses safety risk

    Mercedes-Benz recalls 2019-2023 G 550 and 2019-2022 G63 AMG vehicles with faulty rear door latches that may fail to engage or prevent door operation, creating crash and injury risks.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G63, G 550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V658000·2024-09-09

    Mercedes-Benz Recalls 2024 GLC Models Due to Engine Carrier Weld Defect

    Mercedes-Benz is recalling 2024 GLC 300 and AMG GLC 43 vehicles because improper welds on the engine carrier may cause loss of vehicle control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300, AMG GLC43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V656000·2024-09-06

    Airstream Recalls 2024 Trade Wind Trailers Due to Fire Risk

    Airstream is recalling 2024 Trade Wind travel trailers because the air conditioner soft start device may overheat, increasing the risk of a fire.

    Product
    AIRSTREAM — AIRSTREAM TRADE WIND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V655000·2024-09-06

    Phoenix Motorcars Transit Buses Recalled for Electrical System Fire Risk

    Phoenix Motorcars is recalling certain 2019-2021 800V Catalyst and 2020-2022 ZX5 transit buses. The vehicle software may cause the radiator fan electrical circuit to overheat, increasing fire risk.

    Product
    PROTERRA — PROTERRA ZX5, CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E076000·2024-09-06

    Holley Sniper 2 EFI Throttle Body Recall for Fuel Leak Risk

    Holley is recalling 736 Sniper 2 EFI Throttle Bodies that may be missing a fuel plug, creating a risk of fuel leaks and fire.

    Product
    FUEL SYSTEM, GASOLINE:FUEL INJECTION SYSTEM:THROTTLEBODY/MANIFOLD recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V653000·2024-09-05

    RAM 1500 Models Recalled for Anti-Lock Brake Software Malfunction

    Chrysler is recalling certain 2019, 2021-2024 RAM 1500 vehicles because a software malfunction in the ABS control module may disable the electronic stability control system, increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide