The Recall Desk

State

US Virgin Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35451–35475 of 73915

  • LowFDA (Drugs)·D-0429-2019·2019-02-13

    Lupin Recalls Bimatoprost Ophthalmic Solution Due to Impurity Failures

    Lupin Pharmaceuticals is recalling Bimatoprost Ophthalmic Solution 0.03% because out-of-specification results were observed for individual and total impurities.

    Product
    Bimatoprost Ophthalmic Solution 0.03%, packaged in a) 5 mL (NDC 68180-429-02) and b) 7.5 mL (NDC 68180-429-03) bottles, Rx only, Manufactured by: Lupin Limited Pithampur (M.P.) 454 775, INDIA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V093000·2019-02-12

    Freightliner Cascadia Recall for Tie-Rod Failure Risk

    Daimler Trucks North America is recalling 2013-2016 Freightliner Cascadia trucks because brake vibrations may cause tie-rod failure, leading to loss of steering.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19062·2019-02-12

    Target Recalls Toddler Unicorn Boots Due to Choking Hazard

    Target is recalling Cat & Jack toddler boots because the unicorn horn can detach, posing a choking hazard to children.

    Product
    Cat & Jack Unicorn "Chiara" Boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V078000·2019-02-11

    Forest River Recalls 2019 Columbus Trailers Due to Hitch Bolt Issue

    Forest River is recalling 2019 Columbus recreational trailers because insufficiently tightened pin box mounting bolts could cause the trailer to separate from the tow vehicle.

    Product
    FOREST RIVER — FOREST RIVER COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V081000·2019-02-11

    Blue Bird Recalls One 2019 Vision Bus for Wheelchair Lift Defect

    Blue Bird is recalling one 2019 Vision bus because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V080000·2019-02-11

    Lakota Recalls 2018-2019 Trailers Due to Incorrect Tire Placard Data

    Lakota is recalling 2018-2019 Bighorn, Charger, Colt, and Livestock Edition trailers because incorrect tire data on the Federal Placard could lead to tire overload and failure.

    Product
    LAKOTA — LAKOTA BIGHORN, CHARGER, COLT, LIVESTOCK EDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V082000·2019-02-11

    Blue Bird Recalls School Buses with Defective Wheelchair Lifts

    Blue Bird is recalling 2015-2019 Vision and All American school buses because a wheelchair lift component may fail, causing the platform to rise too high and increasing the risk of injury.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V085000·2019-02-08

    Forest River Cherokee Recalled for Incorrect Federal Tire Placard Information

    Forest River is recalling 2019 Cherokee recreational trailers because the Federal Placards list incorrect tire size information, which may lead to the installation of insufficient tires.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V064000·2019-02-08

    Isuzu and Chevrolet Trucks Recalled for Odometer Unit Display Error

    Isuzu is recalling 2019 NPR and Chevrolet 4500/5500 trucks because the odometer may display kilometers instead of miles, potentially delaying critical maintenance.

    Product
    CHEVROLET — CHEVROLET, ISUZU LOW CAB FORWARD 4500, NRR, LOW CAB FORWARD 5500, NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V088000·2019-02-07

    GM Recalls 2016-2018 Silverado and Sierra 3500 Trucks for Fuel Tank Fire Risk

    General Motors is recalling 2016-2018 Chevrolet Silverado 3500 and GMC Sierra 3500 trucks because a fuel sensor defect may cause the front tank to overfill, potentially leading to a fuel leak and fire.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 3500, SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V066000·2019-02-07

    Freightliner Recalls Cascadia Trucks Due to Air Bag Deployment Risk

    Daimler Trucks is recalling 2018-2020 Freightliner Cascadia trucks because the driver's frontal air bag may deploy unexpectedly, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V086000·2019-02-07

    GM Recalls 2016-2018 Cadillac and Chevrolet Vehicles for Steering Defect

    General Motors is recalling specific 2016-2018 Cadillac and Chevrolet vehicles because the electric power steering system may fail, increasing crash risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET CTS, CAMARO, CORVETTE, ATS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0412-2019·2019-02-06

    Prinston Recalls Irbesartan and Hydrochlorothiazide Tablets Due to NDEA Impurity

    Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because FDA testing found the impurity NDEA above acceptable limits.

    Product
    IRBESARTAN AND HYDROCHLOROTHIAZIDE — IRBESARTAN AND HYDROCHLOROTHIAZIDE (IRBESARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0410-2019·2019-02-06

    Prinston Recalls Irbesartan and Hydrochlorothiazide Tablets Due to NDEA Impurity

    Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    IRBESARTAN AND HYDROCHLOROTHIAZIDE — IRBESARTAN AND HYDROCHLOROTHIAZIDE (IRBESARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide