The Recall Desk

State

US Virgin Islands product recalls

73,738 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37951–37975 of 73916

  • LowFDA (Drugs)·D-0907-2018·2018-07-11

    Equate ClearLAX Recalled for Unfiled NDC Numbers on Labeling

    Lupin Somerset is recalling Equate ClearLAX laxative bottles due to unfiled NDC numbers on the labels. This is a Class III recall with no reported health risks.

    Product
    Equate ClearLAX, Polyethylene Glycol 3350 Powder for Solution, OS Osmotic Laxative, OTC, packaged in a) 119 g bottle (NDC 49035-312-07), b) 238 g bottle (NDC 49035-312-08), Distributed by: Wal-mart Stores, Inc., Bentonville, AR 72716
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V458000·2018-07-10

    MV Agusta Recalls 2018 Motorcycles Due to Fork Axle Thread Damage

    MV Agusta is recalling 2018 Brutale 800 Dragster RC, F3 800, and F3 800 RC motorcycles because damaged fork axle threads may cause wheel clamping screw play and loss of control.

    Product
    MV AGUSTA — MV AGUSTA BRUTALE 800 DRAGSTER RC, F3 800, F3 800 RC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V457000·2018-07-10

    Mercedes-Benz Recalls 2017 AMG G65 for Reverse Speed Software Defect

    Mercedes-Benz is recalling 2017 AMG G65 vehicles because incorrect reverse speed limitation software may cause instability and rollover risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G65
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18185·2018-07-10

    Ortovox Recalls Avalanche Transceivers Due to Software Error

    Ortovox is recalling about 20,000 avalanche transceivers because a software error may prevent them from transmitting survivor location data, delaying rescue efforts.

    Product
    Avalanche transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V452000·2018-07-06

    Nissan Recalls 2007-2008 Versa Models Due to Air Bag Inflator Defect

    Nissan is recalling 2007-2008 Versa sedans and hatchbacks because the passenger air bag inflators may explode. This defect could cause metal fragments to strike occupants, resulting in serious injury or death.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V453000·2018-07-06

    BMW Recalls 2018-2019 X3 and X4 Models for Brake Caliper Defect

    BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because insufficient coating on rear brake caliper pistons may reduce braking performance.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V446000·2018-07-05

    Entegra Recalls 2019 Motorhomes for Windshield Wiper Defect

    Entegra is recalling 2019 Emblem and Vision motorhomes because windshield wiper arms may lift at highway speeds, reducing visibility and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA EMBLEM, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V449000·2018-07-05

    Jayco Recalls 2019 White Hawk Trailers Due to Ladder Screw Defect

    Jayco is recalling 2019 White Hawk recreational trailers because screws securing ladder steps may break, posing a fall risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V451000·2018-07-05

    Jayco Recalls 2018-2019 Motorhomes Due to Incorrect Cargo Capacity Label

    Jayco is recalling 2018-2019 Alante, Precept, Seneca, Redhawk, and Melbourne motorhomes because the cargo capacity label overstates limits, increasing crash risk.

    Product
    JAYCO — JAYCO PRECEPT, REDHAWK, ALANTE, SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V445000·2018-07-05

    Jayco Recalls 2019 Alante and Precept Motorhomes for Wiper Defect

    Jayco is recalling 2019 Alante and Precept motorhomes because windshield wiper arms may lift at highway speeds, reducing visibility and increasing crash risk.

    Product
    JAYCO — JAYCO PRECEPT, ALANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·18V448000·2018-07-05

    Keystone Recalls 2018-2019 Dutchmen Aerolite Trailers for Incorrect Rim Label

    Keystone RV Company is recalling 2018-2019 Dutchmen Aerolite recreational trailers because the Federal Certification Label lists the wrong rim size, which could lead to unsafe rim replacements.

    Product
    DUTCHMEN — DUTCHMEN AEROLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2301-2018·2018-07-04

    Philips OmniDiagnost X-ray System Recalled for Tilt Actuator Failure Risk

    Philips is recalling 477 OmniDiagnost Classic X-ray systems because a broken tilt actuator could cause the table to rotate uncontrollably, posing a risk of injury.

    Product
    OmniDiagnost Classic X-ray system Angiographic and Diagnostic, Product Nos. 70859, 708023, 708024, 708025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2281-2018·2018-07-04

    Konica Minolta CS-7 Medical Device Recall Due to Laptop Fire Risk

    Konica Minolta is recalling CS-7 medical devices because the Panasonic Toughbook laptops used in some configurations have a potential battery ignition risk.

    Product
    CS-7, Model No. A4C1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2300-2018·2018-07-04

    Philips OmniDiagnost-Eleva X-ray System Recalled Due to Table Rotation Hazard

    Philips is recalling 508 OmniDiagnost-Eleva X-ray systems because a broken actuator fixation can cause the table to rotate uncontrollably, posing a risk of injury.

    Product
    OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic, Product Nos. 708026, 708027, 708028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2323-2018·2018-07-04

    St Jude Medical Recalls Promote Quadra ICDs for Security Firmware Update

    St Jude Medical is recalling Promote Quadra implantable cardiac devices to release new firmware that strengthens security against unauthorized access.

    Product
    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2320-2018·2018-07-04

    St Jude Medical Recalls Fortify ICDs and CRT-Ds for Security Firmware Update

    St Jude Medical is recalling Fortify ICDs and CRT-Ds to release new firmware that strengthens security against unauthorized access. Older devices may require permanent disabling of RF communication.

    Product
    Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2287-2018·2018-07-04

    Teleflex Universal Shears Recalled Due to Handle Melting During Sterilization

    Teleflex Medical Europe Ltd is recalling 573 units of Pilling Universal Shears because incorrect plastic was used for the handles, causing them to melt during sterilization.

    Product
    Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general surgical scissors
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2313-2018·2018-07-04

    Siemens Artis zee MP Recall for Display Failure After Power Save

    Siemens is recalling Artis zee MP systems because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.

    Product
    Artis zee MP, Material no. 10094139, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide