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.

54951–54975 of 74002

  • ModerateFDA (Food)·F-1768-2015·2015-04-08

    Health One Pharmaceuticals Recalls Ultra Lecithin Dietary Supplements

    Health One Pharmaceuticals is recalling Ultra Lecithin dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Ultra Lecithin
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1365-2015·2015-04-08

    Medtronic Recalls Trellis 6 and 8 Peripheral Infusion Systems for Sterility Breach

    Medtronic is voluntarily recalling Trellis 6 and 8 Peripheral Infusion Systems due to potential sterility breaches in the outer packaging.

    Product
    Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V01, BVT608030V01, BVT612010V01, BVT612030V01, CVT808015, CVT808025, CVT812015, CVT812025, EVT808015, EVT808025, EVT812015, EVT812025, BVT808015, BVT808030, BVT812015, BVT812030…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1706-2015·2015-04-08

    Health One Pharmaceuticals Recalls Cardiospecs Dietary Supplements

    Health One Pharmaceuticals is recalling Cardiospecs dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    Cardiospecs
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1688-2015·2015-04-08

    Health One Pharmaceuticals Recalls Gamma Zyme Dietary Supplements

    Health One Pharmaceuticals is recalling Gamma Zyme dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Gamma Zyme, 100 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1753-2015·2015-04-08

    Health One Recalls Reishi Mushroom Capsules for cGMP Violations

    Health One Pharmaceuticals is recalling Reishi Mushroom capsules due to significant violations of dietary supplement manufacturing regulations.

    Product
    Reishi Mushroom, 90 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1633-2015·2015-04-08

    Health One Pharmaceuticals Recalls Shu Chang Bao Dietary Supplements

    Health One Pharmaceuticals is recalling Shu Chang Bao dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Shu Chang Bao, 150 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1738-2015·2015-04-08

    Health One Pharmaceuticals Recalls Motichi Dietary Supplements

    Health One Pharmaceuticals is recalling Motichi dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Motichi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E029000·2015-04-07

    Lippert Trailer Axle Hubs Recalled for Wheel Stud Failure Risk

    Lippert Components is recalling specific trailer axle hubs because wheel mounting studs may fail, potentially causing wheel separation and a crash.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V208000·2015-04-07

    Hino Recalls 2015-2016 Trucks Due to Front Axle U-Bolt Defect

    Hino is recalling 2015-2016 238, 258, 268, and 338 trucks because overtightened front axle U-bolts may fail, causing loss of steering.

    Product
    HINO — HINO 238, 268, 258, 338
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V207000·2015-04-07

    Keystone and Dutchmen Trailers Recalled for Wheel Stud Defect

    Keystone RV Company is recalling 2015-2016 Keystone and Dutchmen trailers because wheel studs may break, potentially causing the wheel to detach.

    Product
    DUTCHMEN — DUTCHMEN, KEYSTONE ASPEN TRAIL, DENALI, SPRINTER, SPRINGDALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V209000·2015-04-07

    Highland Ridge RV Recalls 2015-2016 Trailers Due to Slide Room Defect

    Highland Ridge RV is recalling 238 model year 2015-2016 travel and fifth wheel trailers because slide room screws may fail, allowing the room to extend while driving and increasing crash risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW JOURNEYER, LIGHT, MESA RIDGE, ROAMER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V205000·2015-04-06

    BMW Recalls 2005-2008 MINI Cooper Models Due to Air Bag Defect

    BMW is recalling 91,800 MINI Cooper vehicles because the front passenger air bag may not deploy in a crash due to a faulty seat mat.

    Product
    MINI — MINI COOPER S CONVERTIBLE, COOPER CONVERTIBLE, COOPER, COOPER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V204000·2015-04-06

    Autocar Recalls ACX Garbage Trucks Due to Cross Member Bracket Failure

    Autocar is recalling 2013-2015 ACX front-end loader garbage trucks because mounting brackets may fail, causing the cross member to detach and creating road hazards.

    Product
    AUTOCAR — AUTOCAR ACX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V201000·2015-04-06

    GM Recalls 2004 Buick, Chevrolet, and Pontiac Vehicles for Engine Oil Leak

    General Motors is recalling specific 2004 Buick, Chevrolet, and Pontiac vehicles because a leaking valve cover gasket may cause engine oil to drip onto the exhaust manifold, increasing the risk of a fire.

    Product
    CHEVROLET — CHEVROLET, BUICK, PONTIAC IMPALA, REGAL, MONTE CARLO, GRAND PRIX
    Category
    Vehicle
    Distribution
    Distributed nationwide