The Recall Desk

State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

61026–61050 of 74011

  • SevereCPSC·14023·2013-11-19

    Viking Recalls Built-In Refrigerator Freezers Due to Fire Hazard

    Viking is recalling about 750 built-in side-by-side refrigerator freezers because electrical connectors can overheat, posing a fire hazard. Consumers should unplug the units and contact Viking for a free repair.

    Product
    Viking built-in side-by-side refrigerator freezers with in-door dispensers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V649000·2013-11-19

    Cruiser RV Recalls Trailers Due to Door Lock Jamming Hazard

    Cruiser RV is recalling 2006-2013 recreational trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside the vehicle.

    Product
    CRUISER RV — CRUISER RV RADIANCE, VIEWFINDER, SIGNATURE, ENTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V574000·2013-11-19

    Spartan Recalls 2013-2014 Utilimaster P80X Vehicles for Defrost Hose Issue

    Spartan Motors is recalling 586 Utilimaster P80X vehicles sold to UPS because a kinked coolant hose may prevent the windshield defrost system from working, reducing visibility.

    Product
    UTILIMASTER — UTILIMASTER P80X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V575000·2013-11-19

    Space Craft Recalls Fifth Wheel Trailers Due to Door Lock Defect

    Space Craft is recalling 2006-2013 fifth wheel and travel trailers equipped with Fastec door locks that may jam, potentially trapping occupants inside.

    Product
    SPACE CRAFT — SPACE CRAFT FIFTH WHEEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V572000·2013-11-18

    Suzuki Recalls 2013 SX4 Vehicles Due to Torque Converter Bolt Defect

    Suzuki is recalling 2013 SX4 vehicles with continuously variable transmissions because torque converter bolts may loosen, potentially causing the engine to stall and increasing crash risk.

    Product
    SUZUKI — SUZUKI SX4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V573000·2013-11-18

    Kenworth T800 and W900 Trucks Recalled for Brake System Defect

    PACCAR is recalling 2007-2014 Kenworth T800 and W900 trucks because brake chambers may take too long to apply or release, increasing crash risk.

    Product
    KENWORTH — KENWORTH W900, T800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V570000·2013-11-15

    BMW Recalls 2013 X3 xDrive Models for Instrument Panel Defect

    BMW is recalling 2013 X3 xDrive 28i/35i vehicles because a production error in the instrument panel could cause the airbag to deploy improperly during a crash.

    Product
    BMW — BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14020·2013-11-15

    Step2 Recalls Ride-On Wagon Toys Due to Fall Hazard

    Step2 is recalling about 14,000 Whisper Ride Touring Wagons because removable seat backs can detach, allowing children to fall out.

    Product
    Step2® Whisper Ride Touring Wagon™
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V571000·2013-11-14

    Honda Recalls 2014 Acura MDX AWD for Drive Shaft Bolt Issue

    Honda is recalling 2014 Acura MDX AWD vehicles because drive shaft bolts may not be properly tightened, which could allow the shaft to detach and increase crash risk.

    Product
    ACURA — ACURA MDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V568000·2013-11-14

    Volkswagen Recalls 2013-2014 Jetta Hybrid Vehicles for Gearbox Corrosion

    Volkswagen is recalling 2013-2014 Jetta Hybrid vehicles because gearbox corrosion may cause an electrical short and sudden loss of power, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0115-2014·2013-11-13

    Yoders Country Market Recalls Honey Roasted Peanuts for Undeclared Allergens

    Yoders Country Market is recalling 24 units of Honey Roasted Peanuts in custom gift boxes because the product contains undeclared milk and wheat.

    Product
    Custom made gift boxes containing: HONEY ROASTED PEANUTS, Net Wt. 11 oz. (311G), Dist.By: Dutch Valley Food Distributors, Inc. Myerstown, PA 10787, UPC 8 77245 00143 3
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-66403-002·2013-11-13

    Mylan Recalls Amlodipine and Benazepril Capsules Due to CGMP Deviations

    Mylan Pharmaceuticals is recalling specific lots of Amlodipine Besylate and Benazepril HCl capsules because they were not manufactured according to Good Manufacturing Practices.

    Product
    Amlodipine Besylate and Benazepril HCl Capsules, 2.5 mg/10 mg, 100-count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A, NDC 0378-6895-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0085-2014·2013-11-13

    Baylis Medical Recalls TorFlex Transseptal Guiding Sheath Kits

    Baylis Medical is recalling TorFlex Transseptal Guiding Sheath Kits because the sheath may remove particulate from the dilator, which could migrate into a patient's bloodstream.

    Product
    Baylis Medical TorFlex Transseptal Guiding Sheath, Rx Only, non-pyrogenic, sterile. Product Usage: The TorFlex Transseptal Guiding Sheath kit (K102948) is a single use device consisting of three components: a sheath, a dilator, and a J-tipped guidewire. The kit is designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0118-2014·2013-11-13

    Irwin Naturals Recalls Dual Action Cleanse Due to Chloramphenicol Contamination

    Irwin Naturals is recalling Dual Action Cleanse and Daily Digestive Enzymes because they may be contaminated with chloramphenicol.

    Product
    Dual Action Cleanse by Cellular Research Formulas, 60 ct, Item AN027370, UPC 7 10363 27370 5, Item AN056592HFS, UPC 7 10363 56592 3; Item DR056439, UPC 7 10363 57369 0.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-66403-004·2013-11-13

    Mylan Recalls Ciprofloxacin Tablets Due to Manufacturing Deviations

    Mylan Pharmaceuticals is recalling 521 bottles of Ciprofloxacin 250 mg tablets because they were not manufactured according to Good Manufacturing Practices.

    Product
    Ciprofloxacin Tablets, USP, 250 mg, 100-count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-7097-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0116-2014·2013-11-13

    GE Pharma Recalls Creafuse Grape Due to DMAA Contamination

    GE Pharma LLC is recalling 480 units of Creafuse Grape, 600 Grams, because the product contains 1,3 dimethylamylamine (DMAA).

    Product
    Creafuse Grape, 600 Grams
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-66403-008·2013-11-13

    Mylan Recalls Amlodipine and Benazepril Capsules Due to Manufacturing Deviations

    Mylan Pharmaceuticals is recalling specific lots of Amlodipine Besylate and Benazepril HCl capsules because they were not manufactured according to Good Manufacturing Practices.

    Product
    Amlodipine Besylate and Benazepril HCl Capsules, 5 mg/40 mg, 100-count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-6899-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-66403-012·2013-11-13

    Mylan Recalls Amlodipine Besylate Tablets Due to Manufacturing Deviations

    Mylan Pharmaceuticals is recalling Amlodipine Besylate Tablets 10 mg because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.

    Product
    Amlodipine Besylate Tablets, USP 10 mg, packaged in a) 90-count bottles (NDC 0378-5210-77) and b) 500-count bottles (NDC 0378-5210-05), Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0117-2014·2013-11-13

    GE Pharma Recalls Creafuse Fruit Punch for DMAA Content

    GE Pharma LLC is recalling Creafuse Fruit Punch, 600 Grams, because the product contains 1,3 dimethylamylamine (DMAA).

    Product
    Creafuse Fruit Punch, 600 Grams
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-66403-005·2013-11-13

    Mylan Recalls Amlodipine Besylate Tablets Due to CGMP Deviations

    Mylan Pharmaceuticals is recalling Amlodipine Besylate Tablets, 5 mg, because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.

    Product
    Amlodipine Besylate Tablets, USP, 5 mg, packaged in a) 90-count bottles (NDC 0378-5209-77) and b) 500-count bottles (NDC 0378-5209-05), Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide