The Recall Desk

State

US Virgin Islands product recalls

73,824 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
178
Critical
12
Severe
39
Most recent
2026-10-21

Of the 178 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 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53501–53525 of 74002

  • HighNHTSA·15V400000·2015-06-23

    Starcraft RV Recalls 2014-2016 Trailers for Incorrect Tire Certification Labels

    Starcraft RV is recalling 50 model year 2014-2016 AR-ONE and Comet trailers because certification labels list the wrong tire size, which could lead to improper tire installation and increased crash risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT, STARCRAFT COMET, AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V397000·2015-06-23

    Forest River Recalls 2015 Dynamax Rev for Head Restraint Defect

    Forest River is recalling 2015 Dynamax Rev vehicles because front head restraints may exceed safety limits, increasing injury risk in rear-end collisions.

    Product
    DYNAMAX — DYNAMAX REV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V396000·2015-06-22

    Turtle Top Transit Buses Recalled for Electrical Fire Risk

    Turtle Top is recalling certain 2006-2014 transit buses and specialty vehicles because a loose electrical connection may cause a fire.

    Product
    TURTLE TOP — TURTLE TOP ODYSSEY LT, ODYSSEY, TERRA TRANSPORT, VANTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V393000·2015-06-22

    Jeep Cherokee Recall: Power Liftgate Module Fire Risk

    Chrysler is recalling 2014-2015 Jeep Cherokee vehicles with power liftgates because water intrusion may cause a short circuit and fire.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V389000·2015-06-19

    MCI Motorcoaches Recalled for Hub Carrier Cracking and Oil Leaks

    Motor Coach Industries is recalling certain 2013-2015 D4500, D4505, and J4500 motorcoaches because hub carriers may crack or leak oil, potentially causing loss of vehicle control.

    Product
    MCI — MCI D4505, J4500, D4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15167·2015-06-19

    PetSmart Recalls Top Fin Plastic Aquarium Heaters Due to Electrical Shock Hazard

    PetSmart is recalling Top Fin plastic aquarium heaters due to an electrical problem that poses a risk of fire or electrical shock. Consumers should stop using the heaters and return them for a full refund.

    Product
    Top Fin Plastic Aquarium Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V390000·2015-06-19

    Forest River Recalls Trailers Due to Wheel Stud Breakage Risk

    Forest River is recalling specific model years of Auto Plus, Sandpiper, Vengeance, Cargo Mate, Hydra-Lift, and XLR trailers because wheel studs may break, potentially causing the wheel to detach.

    Product
    FOREST RIVER — FOREST RIVER HYDRA-LIFT, VENGEANCE, CARGO MATE, XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V391000·2015-06-19

    Champion Transit Bus Recall for Fraying Seat Belts

    Champion is recalling 2013-2015 transit buses because seat belts may rub against metal frames and fray, failing federal safety standards.

    Product
    CHAMPION — CHAMPION AMERICAN COACH, SPIRIT, AMERICAN CRUSADER, LF TRANSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V386000·2015-06-17

    Land Rover Recalls LR4 Vehicles Due to Sunroof Adhesive Defect

    Jaguar Land Rover is recalling 2012-2013 LR4 vehicles because the panoramic roof adhesive may not secure the assembly, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER LR4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V385000·2015-06-17

    Land Rover Recalls Range Rover Models for Door Latch Defect

    Jaguar Land Rover is recalling 2013-2016 Range Rover and 2014-2016 Range Rover Sport vehicles because doors may unlatch unexpectedly, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1767-2015·2015-06-17

    Philips Medical Systems Recalls Extended Brilliance Workstation UPS Accessories

    Philips Medical Systems is recalling Extended Brilliance Workstation UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.

    Product
    Extended Brilliance Workstation (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1131-2015·2015-06-17

    Baxter Recalls Subpotent Heparin Sodium Injection Due to Raw Material Issues

    Baxter Healthcare is recalling specific lots of Heparin Sodium in Sodium Chloride Injection because the raw material was found to be subpotent and out of specification.

    Product
    HEPARIN SODIUM IN SODIUM CHLORIDE — HEPARIN SODIUM IN SODIUM CHLORIDE (HEPARIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1750-2015·2015-06-17

    ResMed Astral Ventilator Recall Due to Alarm Disabling Hazard

    ResMed is recalling Astral 100 and 150 ventilators because clinicians can disable all alarms, including circuit disconnection alerts, posing a risk of insufficient ventilation.

    Product
    Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1130-2015·2015-06-17

    Akorn Recalls Hydroxyzine Hydrochloride Oral Solution Due to Impurities

    Akorn, Inc. is recalling Hydroxyzine Hydrochloride oral solution because it failed impurities and degradation specifications. The product was distributed nationwide, including Puerto Rico.

    Product
    Hydroxyzine Hydrochloride, oral solution, 10 mg per 5 mL, 16 fl oz (473 ml) bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co., Inc., Amityville, NY, NDC 50383-0796-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1738-2015·2015-06-17

    Smith & Nephew R3 Constrained Liner Recalled for Locking Groove Defect

    Smith & Nephew is recalling 40 units of R3 Constrained Liners because the locking groove is oversized, preventing the locking ring from engaging properly.

    Product
    R3(TM) 28 MM I.D., 60 MM O.D. CONSTRAINED LINER, REF 71339160, QTY: (1), STERILE EO, Product Usage: The R3 Constrained liner Acetabular System is a cemented or uncemented prosthesis intended to replace a hip joint. The Constrained liner is intended for primary or revision…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1716-2015·2015-06-17

    Fresenius CRIT-LINE Blood Chamber Recalled for Connection Leaks

    Fresenius Medical Care is recalling CRIT-LINE Blood Chambers because the connection may leak during use.

    Product
    CRIT-LINE Blood Chamber- an accessory to the Crit line III- Monitors in real time blood parameters Model: CL10021021
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1770-2015·2015-06-17

    Philips Ingenuity Flex UPS Accessory Devices Recalled for Battery Acid Leakage

    Philips Medical Systems is recalling 23 Ingenuity Flex UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.

    Product
    Ingenuity Flex (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1779-2015·2015-06-17

    Philips Precedence 6 UPS Accessory Devices Recalled for Battery Acid Leakage

    Philips Medical Systems is recalling Precedence 6 UPS accessory devices for CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.

    Product
    Precedence 6 (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1699-2015·2015-06-17

    Zimmer Recalls M/L Taper Hip Stems Due to Cytotoxicity Levels

    Zimmer is voluntarily recalling 752 M/L Taper hip implants because they contain higher than allowed cytotoxicity levels, posing a risk of adverse biological response.

    Product
    M/L Taper with Kinectiv¿ Technology. prosthesis, hip, semi-constrained (metal uncemented acetabular component) Product Usage: Usage: Total hip replacement for the following: severe hip pain and disability due to rheumatoid arthritis, osteoarthritis, traumatic arthritis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1781-2015·2015-06-17

    Philips Gemini GXL 16 Slice CT Systems Recalled for UPS Battery Hazards

    Philips is recalling 15 Gemini GXL 16 Slice CT systems worldwide because their UPS accessory devices may leak battery acid, overheat, or emit fumes.

    Product
    Gemini GXL 16 Slice (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide