The Recall Desk

State

US Virgin Islands product recalls

73,219 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 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18026–18050 of 73396

  • ModerateFDA (Devices)·Z-0362-2023·2022-12-14

    IgA and IgM Immunoturbidimetric Assay Testing Order Carryover Avoidance Update

    Randox Laboratories updated its carryover avoidance protocol for IgA and IgM immunoturbidimetric assays. Running these assays immediately after Fructosamine tests on RX instruments can cause falsely elevated results (up to +13% for IgA, +51% for IgM).

    Product
    IgA Immunoturbidimetric Assay- In vitro determination of IgA and IgM in serum and plasma Catalog Number: IA3832
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0406-2023·2022-12-14

    Bipolar Forceps Recall: Missing Instructions for Power Supply and Maintenance

    CareFusion bipolar forceps are being recalled due to missing Instructions for Use content about power supply interface, cleaning, and maintenance. Users should obtain the complete manufacturer instructions immediately.

    Product
    CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5069
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0388-2023·2022-12-14

    Bipolar Irrigating Forceps Recall: Missing Power Supply and Maintenance Instructions

    Carefusion is recalling 132 units of V. Mueller bipolar irrigation forceps due to incomplete instruction manuals missing power supply interface and maintenance guidance.

    Product
    Carefusion V. Mueller SCOVILLE-GREENWOOD BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED, 1.5MM TIP OVERALL LENGTH 7-3/4" (195MM), REF F-1305
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0424-2023·2022-12-14

    HF Resection Electrodes Recalled for Incompatible Packaged Cable

    Olympus Corporation is recalling HF Resection Electrodes because an incompatible cable may be included in packaging. The cable cannot connect to the electrosurgical generator, potentially delaying or canceling surgery.

    Product
    HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0414-2023·2022-12-14

    CareFusion Bipolar Surgical Forceps Recalled for Incomplete Instructions

    CareFusion bipolar surgical forceps are being recalled because their instruction manual is missing critical information about power supply interface and cleaning procedures. BD is providing corrected instructions to healthcare facilities.

    Product
    CareFusion V. Mueller TITANIUM BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED STRAIGHT FINE, 0.5MM TIP OVERALL LENGTH 8-3/4" (225MM), REF F-5302
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0404-2023·2022-12-14

    Bipolar Forceps Device Incomplete Instructions for Use Recalled

    CareFusion bipolar forceps (REF F-5061) recalled due to incomplete Instructions for Use missing device power supply interface and cleaning instruction content.

    Product
    CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH 9-1/2" (240MM), REF F-5061
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0386-2023·2022-12-14

    Bipolar Surgical Forceps Recalled for Incomplete Instructions for Use

    Carefusion bipolar surgical forceps recalled nationwide due to incomplete Instructions for Use. The distributed IFU is missing guidance on power supply interface and cleaning and maintenance procedures.

    Product
    Carefusion V. Mueller GERALD BAYONET BIPOLAR FORCEPS 1.0MM TIP, INSULATED IRRIGATING OVERALL LENGTH 7-1/2" (190MM), REF F-1303
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0402-2023·2022-12-14

    Medical Device Recall: Missing Instructions for Bipolar Surgical Forceps

    CareFusion bipolar forceps recalled because the provided instructions are missing critical information about power supply interface and cleaning procedures. No injuries reported.

    Product
    CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS,1.0MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5018
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V921000·2022-12-13

    2021 Porsche Taycan Suspension Strut Defect May Cause Loss of Vehicle Control

    A retaining ring on the 2021 Porsche Taycan's suspension strut may come loose, causing loss of vehicle control and increasing crash risk. Repairs will be provided free by Porsche dealers.

    Product
    PORSCHE — PORSCHE TAYCAN, TAYCAN 4S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V922000·2022-12-13

    2023 Jayco Solstice defrost controls may fail, increasing crash risk

    Jayco is recalling 2023 Solstice and Entegra Expanse recreational vehicles because the HVAC system's defrost and defog controls may stop working. This loss of visibility control increases the risk of crashes under certain driving conditions.

    Product
    ENTEGRA — ENTEGRA, JAYCO EXPANSE, SOLSTICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V920000·2022-12-13

    2023 Forest River Travel Trailers Recalled for Refrigerator Wiring Fire Risk

    Forest River is recalling certain 2023 Wildwood, Salem, and Stealth EVO travel trailers. The 8-gauge refrigerator wire lacks over-current protection, creating a fire risk from melted wiring.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, STEALTH EVO, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V917000·2022-12-12

    Volvo Bus 9700 Recalled for GPS Installation Defect

    Volvo Bus is recalling 2022 9700 buses because incorrectly installed GPS devices may cause accelerator sensor malfunction and loss of drive power.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23066·2022-12-12

    Art of Green Laundry Detergent Recalled for Bacterial Contamination

    AlEn USA is recalling Art of Green laundry detergent products because they may contain Pseudomonas aeruginosa bacteria, which can cause serious infection in people with weakened immune systems or external medical devices.

    Product
    Art of Green laundry detergent products
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V919000·2022-12-12

    Freightliner and Western Star trucks recalled for tire incompatibility

    Daimler Trucks is recalling certain Freightliner and Western Star commercial trucks with tires incompatible with their 8.25-inch rims. Incompatible tires can reduce performance and increase crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 122SD, 114SD, BUSINESS CLASS M2, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V912000·2022-12-09

    Kawasaki Recalls Motorcycles Due to Camshaft Chain Tensioner Defect

    Kawasaki is recalling specific 2015-2023 motorcycles because a defective camshaft chain tensioner may lock, causing the engine to stall while riding.

    Product
    KAWASAKI — KAWASAKI NINJA H2, NINJA 1000, ZR1002L, ZR1000K
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V911000·2022-12-09

    Braun Ambulances Recall 2014-2022 Models Due to HVAC Fire Risk

    Braun Ambulances is recalling 1,321 vehicles from 2014-2022 because a faulty relay may cause the HVAC system to overheat, increasing the risk of a fire.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES PATRIOT, EXPRESS, CHIEF XL, SIGNATURE SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V905000·2022-12-08

    Hyundai Translead Recalls 2020-2021 Trailers Due to Brake Pad Retaining Clip Defect

    Hyundai Translead is recalling 2020-2021 Dry Van and Reefer Trailers because a loose brake pad retaining clip may detach, reducing brake performance or causing a flat tire.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD REEFER TRAILER, DRY VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V908000·2022-12-08

    2023 McLaren Artura recalled for fuel pipe defect increasing fire risk

    McLaren is recalling 164 2023 Artura vehicles because high-pressure fuel pipe nuts may loosen, causing fuel leaks that could lead to fires. Dealers will replace the fuel pipes at no cost.

    Product
    MCLAREN — MCLAREN ARTURA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23065·2022-12-08

    Ortal Gas Fireplaces Recalled Due to Fire Hazard Risk

    Ortal USA is recalling about 400 Traditional 90 and Traditional 110 gas fireplaces due to improper installation that can cause fire hazards. The firm has received four reports of installation errors resulting in fires with property damage.

    Product
    Traditional 90 and Traditional 110 Gas Fireplaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide