The Recall Desk

State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57951–57975 of 74005

  • ModerateFDA (Devices)·Z-1937-2014·2014-07-09

    Zimmer Recalls NexGen Knee Components Due to Thread Specification Issues

    Zimmer is voluntarily recalling specific lots of NexGen Complete Knee Solution stemmed tibial components because the threads may be out of specification.

    Product
    NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 6. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1943-2014·2014-07-09

    Blue Belt Technologies Recalls Mislabeled Stride Femoral Knee Components

    Blue Belt Technologies is recalling two lots of Stride Femoral Knee Components due to packaging mislabeling that could lead to the implantation of the wrong side or size.

    Product
    Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1949-2014·2014-07-09

    DeVilbiss DV5x Series CPAP Units Recalled for Missing Serial Numbers

    DeVilbiss Healthcare LLC is recalling 1,809 DV5x Series CPAP units because they were shipped without programmed serial numbers, displaying 'RUN-TEST' on the screen.

    Product
    DeVilbiss Model DV5x Series CPAP units. For use in treating Obstructive Sleep Apnea (OSA) by means of application of positive air pressure. Used in home and clinical environments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V411000·2014-07-08

    J.C. Madigan Recalls Two Ford Dump Trucks for Fire Risk

    J.C. Madigan is recalling two specific Ford dump trucks because a leaking pressure switch may cause a fire near the exhaust system.

    Product
    FORD — FORD F-550, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V408000·2014-07-07

    Genuine Scooter Recalls 2014 Stella 125 Automatic for Engine Stalling Risk

    Genuine Scooters is recalling 2014 Stella 125 Automatic scooters because a faulty engine control unit may cause the engine to stall without warning, increasing crash risk.

    Product
    GENUINE SCOOTER — GENUINE SCOOTER STELLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V412000·2014-07-07

    Volkswagen Recalls 2015 Golf and GTI for Steering Interference Risk

    Volkswagen is recalling 2015 Golf and GTI vehicles because loose stabilizer link fasteners may interfere with steering, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF, GTI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V400000·2014-07-03

    GM Recalls 5.8 Million Vehicles for Ignition Switch Airbag Risk

    General Motors is recalling 5,877,718 vehicles from 1997-2008 because the ignition switch may move out of the run position, preventing airbags from deploying in a crash.

    Product
    CHEVROLET — CHEVROLET, PONTIAC, OLDSMOBILE IMPALA, GRAND AM, GRAND PRIX, MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E036000·2014-07-03

    Brake Parts Inc. Recalls Rear Wheel Brake Shoes Due to Detachment Risk

    Brake Parts Inc. is recalling specific ACDelco, Carquest, Federated, and Raybestos rear wheel brake shoes because the lining may detach from the steel shoe, potentially reducing braking force or causing wheel lockup.

    Product
    SERVICE BRAKES, AIR:DRUM:SHOES/LININGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2045-2014·2014-07-02

    Navitas Naturals Organic Sprouted Chia Powder Recalled Due to Salmonella

    Navitas Naturals is recalling Organic Sprouted Chia Powder because it is linked to a multistate outbreak of Salmonella Newport.

    Product
    Navitas Naturals Organic Sprouted Chia Powder, 8 oz (227g) package; Omega Fatty Acids, Protein, dietary Fiber. UPC 858847000369; Navitas Naturals, Novato, CA 94949
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2046-2014·2014-07-02

    Navitas Naturals Omega Blend Sprouted Smoothie Mix Recalled for Salmonella

    Navitas Naturals is recalling Omega Blend Sprouted Smoothie Mix because chia products were linked to a multistate Salmonella Newport outbreak.

    Product
    Navitas Naturals Omega Blend Sprouted Smoothie Mix, 8 oz. (227g) package; Dietary Fiber, Raw, Sprouted. UPC 858847000314; Also packaged for Williams Sonoma Omega Smoothie Mixer; SKU 506436 Navitas Naturals, Novato, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2047-2014·2014-07-02

    Navitas Naturals Omega 3 Smoothie Mixer Recalled Due to Salmonella Outbreak

    Navitas Naturals is recalling Omega 3 Smoothie Mixers because chia products were linked to a multistate Salmonella Newport outbreak.

    Product
    William & Sonoma Navitas Naturals brand Omega 3 Smoothie Mixer, 8 oz. (227g) package; Dietary Fiber, Raw, Sprouted.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2050-2014·2014-07-02

    Green Smoothie Girl Recalls TriOmega Superfood Due to Salmonella Risk

    Green Smoothie Girl is recalling TriOmega Superfood products because they contain Organic Sprouted Chia Powder that may be contaminated with Salmonella.

    Product
    GreenSmoothieGirl TriOmega Superfood, GreenSmoothieGirl Sprouted Ground TriIOmega Superfood, Packaged in metalized resealable standup pouches in 1-pound units
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V394000·2014-07-02

    GM Recalls Cadillac CTS and SRX for Ignition Switch Defect

    General Motors is recalling 554,328 Cadillac CTS and SRX vehicles because the ignition switch may move out of the run position, potentially preventing airbags from deploying.

    Product
    CADILLAC — CADILLAC CTS, SRX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1822-2014·2014-07-02

    Nitinol Recalls HydroFinity Hydrophilic Guidewires Due to Jacket Damage

    Nitinol Devices and Components is recalling HydroFinity Hydrophilic Guidewires because reports indicate the outer polymer jacket may be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire; 0.035 OD, Stiff Shaft, Straight Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1820-2014·2014-07-02

    Nitinol HydroFinity Hydrophilic Guidewire Recalled for Outer Polymer Jacket Damage

    Nitinol Devices and Components, Inc. is recalling HydroFinity Hydrophilic guidewires due to reports of the outer polymer jacket being damaged during use.

    Product
    HydroFinity Hydrophilic guidewire;Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled Tip, 260 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1816-2014·2014-07-02

    Nitinol HydroFinity Hydrophilic Guidewire Recalled for Polymer Jacket Damage

    Nitinol Devices and Components, Inc. is recalling HydroFinity Hydrophilic guidewires because the outer polymer jacket may be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile.Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Straight Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V404000·2014-07-02

    GM Recalls 2005-2007 SUVs for Power Window Fire Risk

    General Motors is recalling 2005-2007 Buick, SAAB, Isuzu, Chevrolet, and GMC SUVs because fluid in the power window switch may cause a fire.

    Product
    BUICK — BUICK, SAAB, ISUZU RAINIER, 9-7X, ASCENDER, TRAILBLAZER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1817-2014·2014-07-02

    FDA Recalls HydroFinity Hydrophilic Guidewires Due to Jacket Damage

    Nitinol Devices and Components is recalling HydroFinity Hydrophilic Guidewires because the outer polymer jacket may be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Straight Tip, 260 CM Length Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V405000·2014-07-02

    Ford Recalls 2014 F-53 and F-59 Chassis for Brake Caliper Defect

    Ford is recalling 2014 F-53 and F-59 chassis because incorrectly machined brake calipers may leak fluid, increasing stopping distances and crash risk.

    Product
    FORD — FORD F-53, F-59
    Category
    Vehicle
    Distribution
    Distributed nationwide