The Recall Desk

State

US Virgin Islands product recalls

73,106 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
2026-09-23

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 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12451–12475 of 73283

  • HighFDA (Devices)·Z-1073-2024·2024-02-21

    Philips Recalls ProxiDiagnost Radiography Systems for Patient Data Display and Security Issues

    Philips is recalling 20 ProxiDiagnost radiography/fluoroscopy systems due to two issues: potential display of previous patient images when scanning new patients, and a security vulnerability allowing unauthorized data access. No injuries have been reported.

    Product
    ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V126000·2024-02-21

    Spencer Recalls 2020 Pumper Fire Trucks Due to Electrical Fire Risk

    Spencer is recalling 2020 Pumper fire trucks because a firmware defect in Weldon nodes may cause overloaded electrical circuits, increasing the risk of fire.

    Product
    SPENCER — SPENCER PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1072-2024·2024-02-21

    Philips ProxiDiagnost N90 X-ray System Recall for Patient Data and Security Issues

    Philips is recalling 138 U.S. units of its ProxiDiagnost N90 radiography system due to two identified issues. The system may display incorrect patient images during scan transitions, and a security vulnerability could allow unauthorized data access with physical device access.

    Product
    ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1139-2024·2024-02-21

    BIOFIRE BCID2 Blood Culture Panel Recalled for False Positive Candida tropicalis Results

    BioFire Diagnostics recalls BIOFIRE BCID2 panels due to false positive Candida tropicalis detection when used with certain BD BACTEC culture vials. The vials contain non-viable organism DNA that triggers incorrect positive results.

    Product
    BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds Plus medium BD BACTEC Plus Aerobic medium BD BACTEC Plus Anaerobic medium BD BACTEC Standard Aerobic medium BD BACTEC Standard Anaerobic medium The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1056-2024·2024-02-21

    Samsung GM85 Mobile X-ray System Welding Frame Defect Arm Fall Risk

    NeuroLogica is recalling 261 Samsung GM85 mobile x-ray systems due to a welding defect in the moving arm frame that could cause the arm to fall, risking bodily injury.

    Product
    Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1088-2024·2024-02-21

    Philips CombiDiagnost R90 Fluoroscopy Display May Show Previous Patient Images

    Philips CombiDiagnost R90 fluoroscopy systems may display a previous patient's images during radiography examination, potentially showing different image content, format, and size that could affect imaging accuracy.

    Product
    CombiDiagnost R90 1.1 (709031)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1077-2024·2024-02-21

    Medical Device Recall: Heart-Lung Machine Component Sterile Barrier Defect

    The BEQ-HLS 7050 USA HLS Set Advanced 7.0 is recalled due to a compromised sterile barrier on its Emergency Priming Line component. This defect may cause inflammation, sepsis, or infection.

    Product
    BEQ-HLS 7050 USA, HLS Set Advanced 7.0, Product Code/Part Number 70106.9078. Used with the CARDIOHELP heart-lung machine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0324-2024·2024-02-21

    HydrALAZINE Hydrochloride Tablets Recalled for Out-of-Specification Impurities

    HydrALAZINE Hydrochloride Tablets Lot T04680 are recalled for out-of-specification impurities found during routine testing. No illnesses have been reported, but the product poses a remote risk of reversible effects.

    Product
    HydrALAZINE Hydrochloride Tablets, USP 10mg, packaged in 100-count (10x10 blister cards), Lot T04680, Rx only, Manufactured for Heritage Pharmaceuticals, Inc. Eatontown, NJ, Distributed by Major Pharmaceuticals Livonia MI. NDC 0904-6440-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0322-2024·2024-02-21

    Nortrel 7/7/7 Oral Contraceptive Recalled for Discolored Tablets

    Teva Pharmaceuticals is recalling Nortrel 7/7/7 oral contraceptive tablets due to a manufacturing defect: discolored blue tablets mixed with white inert tablets. This could cause confusion about which tablets to take in the triphasic regimen.

    Product
    NORTREL 7/7/7 — NORTREL 7/7/7 (NORETHINDRONE AND ETHINYL ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1086-2024·2024-02-21

    Quidel Sofia 2 Flu + SARS Test Kits Recalled for Incorrect Expiration Dates

    Quidel Corporation is recalling one lot of Sofia 2 Flu + SARS Antigen FIA diagnostic test kits due to incorrect expiration dates on packaging. Kits labeled to expire April 30 and May 31, 2025 actually expire September 12, 2024.

    Product
    The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence technology in a sandwich design that is used with Sofia 2 to detect nucleocapsid protein from influenza A, influenza B, and SARS-CoV-2. This test allows for the detection of SARS-CoV and SARS-CoV-2, but does not…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1084-2024·2024-02-21

    Stryker Neurovascular Trevo Pro Microcatheter Recalled for Unevaluated Use Statement

    Stryker is recalling the Trevo Pro 18 Microcatheter because its instruction manual contains an intended use that the FDA has not evaluated. The recall affects 11 units distributed across the United States.

    Product
    Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0321-2024·2024-02-21

    Nortrel Oral Contraceptive Tablets Recalled for Discolored Inert Remainder Tablets

    Teva Pharmaceuticals is recalling 12,916 cartons of Nortrel oral contraceptive tablets nationwide due to discolored inert remainder tablets that may cause confusion. Affected lot: #100042978, expiration 7/31/2024.

    Product
    NORTREL — NORTREL (NORETHINDRONE AND ETHINYL ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V123000·2024-02-20

    Porsche 911 rear seat belts may not secure a child restraint

    Porsche is recalling certain 2023 911 vehicles over the rear three-point seat belts, where an unsecured child restraint system can increase the risk of injury in a crash.

    Product
    PORSCHE — PORSCHE 911 CARRERA, 911 CARRERA S, 911 TARGA 4S, 911 TURBO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V121000·2024-02-19

    Volvo Recalls 2024-2025 VNL and VNR Trucks for Steering Defect

    Volvo Trucks is recalling 2024-2025 VNL and VNR models because improperly heat-treated steering gear shafts may crack, risking loss of steering control.

    Product
    VOLVO — VOLVO VNL, VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V120000·2024-02-19

    2023–2024 Horton Ford Emergency Vehicles Brake Line Recall

    Halcore Group, Inc. is recalling certain 2023–2024 Horton emergency vehicles built on Ford F-450, F-550, and F-600 chassis because the left rear brake line can contact and be damaged by the strut mount when the rear suspension is lowered, risking brake fluid leakage and loss of brakes.

    Product
    HORTON — HORTON FORD F-450, FORD F-600, FORD F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V122000·2024-02-19

    2024 Mack Granite trucks recalled for insufficient air brake tank volume

    Mack Trucks is recalling certain 2022–2024 Granite vehicles because the air tanks do not have sufficient volume for the brake system, reducing braking performance and increasing crash risk.

    Product
    MACK — MACK GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V115000·2024-02-16

    Mercedes-Benz Recalls 31,848 Vehicles for Defective 80-Amp Fuses

    Mercedes-Benz is recalling 31,848 vehicles because defective 80-Amp fuses may fail, causing loss of drive power, safety functions, or fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S 580, S 580 E 4MATIC, AMG EQS, S 680
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V117000·2024-02-16

    Mercedes-Benz Recalls 2024 GLE Models Due to Accelerator Pedal Bracket Defect

    Mercedes-Benz is recalling 2024 GLE 350, GLE 450, and AMG GLE53 vehicles because an improperly welded accelerator pedal bracket may break or detach, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLE53 4MATIC+, GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24118·2024-02-15

    Bell Soquel Youth Bicycle Helmets Recalled for Head Injury Risk

    Bell Sports is recalling about 2,425 Bell Soquel Youth Helmets because the strap anchor can become dislodged during a crash, reducing protection and posing a risk of head injury.

    Product
    Bell Soquel Youth Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V111000·2024-02-15

    Jeep Wrangler Defrosting System Software Error May Impair Visibility

    Chrysler is recalling affected Jeep Wrangler and Grand Cherokee models due to a software defect in the windshield defroster system that may reduce visibility. Affected owners should contact Chrysler for a free software update.

    Product
    JEEP — JEEP GRAND CHEROKEE, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V114000·2024-02-15

    2023-2024 Honda Odyssey and 2024 Acura RDX steering defect

    Honda is recalling certain 2023-2024 Odyssey and 2024 Acura RDX vehicles due to improper steering gear box assembly tightening. Water can enter the assembly, causing corrosion and loss of steering control.

    Product
    HONDA — HONDA, ACURA ODYSSEY, RDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24117·2024-02-15

    Frigidaire Rear-Controlled Ranges Recalled for Electrical Shock and Electrocution Hazards

    Electrolux Group is recalling about 1,800 Frigidaire rear-controlled ranges because the control panel can detach from the unit, creating electrical shock and electrocution hazards. Consumers should stop using the ranges immediately and contact Electrolux for a free repair.

    Product
    Frigidaire rear-controlled ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide