The Recall Desk

State

US Virgin Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50051–50075 of 73995

  • HighFDA (Devices)·Z-0817-2016·2016-02-24

    Nihon Kohden MEE-1000A Neuromaster Accessories Recalled for Defective Circuit Boards

    Nihon Kohden America Inc is recalling MEE-1000A Neuromaster accessories due to defective printed circuit boards that failed to prevent unintentional current flow.

    Product
    MEE-1000A Neuromaster, Model No. Accessories: MS-110B (Electric Stimulation), MS-120BK (Current Stimulator Box) JB-116B, JB-132B (Amplifiers) Electromyography. (EMG)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0814-2016·2016-02-24

    CareFusion Recalls Jadak Barcode Scanners for Pyxis Anesthesia Systems

    CareFusion 303, Inc. is recalling 9,345 Jadak Barcode Scanners used with Pyxis Anesthesia systems because they may transmit incorrect medication information to the dispensing system.

    Product
    Jadak Barcode Scanner, Part No. 350587-32, 350587-41, 351377-32. Product Usage: An accessory for the Pyxis Anesthesia ES system and Pyxis Anesthesia system 4000 stations. The Jadak Barcode Scanner is used to scan medication labels during refill of the Pyxis Anesthesia ES…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V105000·2016-02-24

    Isuzu Recalls 2016 Trucks Due to Certification Label Errors

    Isuzu is recalling certain 2016 NPR-HD, NPR-XD, NQR, and NRR trucks because typographical errors on the certification label may prevent accurate vehicle loading and maintenance.

    Product
    ISUZU — ISUZU NPR HD, NPR XD, NQR, NRR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0808-2016·2016-02-24

    Leica Bond Polymer Refine Red Detection Kits Recalled for Staining Errors

    Leica Microsystems is recalling Bond Polymer Refine Red Detection kits due to a manufacturing error that may cause inadequate staining.

    Product
    Bond Polymer Refine Red Detection DS9390 kits. The common name of the device is detection system for in vitro diagnostic use. The Intended Use states that Bond Polymer Refine Red Detection is a biotin-free, polymeric alkaline phosphatase (AP)-linker antibody conjugate system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0665-2016·2016-02-24

    Bonita Pharmaceuticals Recalls Menthocin Patch with Lidocaine-Strong

    Bonita Pharmaceuticals is recalling Menthocin Patch with Lidocaine-Strong because it was marketed without an approved NDA or ANDA.

    Product
    Menthocin Patch with Lidocaine-Strong (Menthol 5%, Capsaicin 0.0375%, Methyl Salicylate 20%, Lidocaine 0.5%), packaged in a box 15 patches, RX Only, Manufactured for Bonita Pharmaceuticals LLC 6380 Commerce Drive Westland, MI 48185-9120, USA NDC 53598-0012-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0720-2016·2016-02-24

    Dr. Reddy's Recalls Paricalcitol Capsules Due to Breakage and Leakage

    Dr. Reddy's Laboratories is recalling Paricalcitol capsules due to reports of breakage and leakage. The recall covers 4,383 bottles distributed nationwide.

    Product
    PARICALCITOL — PARICALCITOL (PARICALCITOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0812-2016·2016-02-24

    C.R. Bard Recalls Toomey Syringes Due to Open Package Seal

    C.R. Bard is recalling 15,400 units of 70cc Toomey Syringes because a customer reported an open package seal.

    Product
    REF 0038460 Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters, Single Use, Rx Only, Latex Free, 50 units. Product Usage: Product is intended for Resectoscope irrigation, catheter irrigation and Foley catheter inflation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V102000·2016-02-23

    Kawasaki Recalls 2016 Ninja ZX-10R Motorcycles for Steering Bolt Defect

    Kawasaki is recalling 544 model year 2016 Ninja ZX-10R motorcycles because steering damper bracket mounting bolts may break, potentially interfering with steering and increasing crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA ZX-10R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V100000·2016-02-23

    Blue Bird Recalls 2008-2009 Vision School Buses for Fire Risk

    Blue Bird is recalling 733 model year 2008-2009 Vision school buses because a wiring defect may cause the battery cable to overheat, melt, and create a fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V101000·2016-02-23

    Blue Bird Recalls 2009 Vision Transit Buses for Electrical Fire Risk

    Blue Bird is recalling 2009 Vision transit buses with Caterpillar C707 engines because a wiring defect may cause the battery cable to overheat, melt, and create a fire hazard.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V103000·2016-02-23

    Thomas Built Buses Recalls Minotour School Buses for Lighting Defect

    Daimler Trucks North America is recalling 2012-2017 Thomas Built Buses Minotour school buses because a body control module failure may cause loss of exterior lighting or windshield wipers.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·020-2016·2016-02-23

    Ajinomoto Recalls Pork Dumplings Misbranded as Beef

    Ajinomoto Windsor Inc. is recalling approximately 6,000 pounds of Shirakiku Gyoza Dumplings labeled as beef but containing undeclared pork.

    Product
    Ajinomoto Windsor Inc. — Recall Notification Report 020-2016 (Pork Products )
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V099000·2016-02-19

    Mack Trucks Recalls 2012-2016 Models for Driveshaft Cap Nut Defect

    Mack Trucks is recalling 33,981 model year 2012-2016 trucks because a cap nut may loosen, causing the driveshaft to disconnect and increasing crash risk.

    Product
    MACK — MACK TITAN (TD), PINNACLE (CHU), TERRAPRO (LEU), PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V096000·2016-02-19

    Toyota Recalls RAV4 Models Due to Rear Seat Belt Cut Risk

    Toyota is recalling 2006-2012 RAV4 and 2012-2014 RAV4 EV vehicles because rear seat belts may be cut by the seat cushion frame in a frontal collision, increasing injury risk.

    Product
    TOYOTA — TOYOTA RAV4 EV, RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V098000·2016-02-19

    Mack Trucks Recalls 2016-2017 Granite and TerraPro for Steering Defect

    Mack Trucks is recalling 1,187 model year 2016-2017 Granite and TerraPro trucks because a missing roll pin may cause the steering shaft to disconnect, resulting in a complete loss of steering.

    Product
    MACK — MACK TERRAPRO (MRU), GRANITE (GU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V095000·2016-02-19

    Volvo Trucks Recall 2009-2016 Models for Steering Component Failure Risk

    Volvo Trucks North America is recalling certain 2009-2010 VT and 2016 VNL/VNM trucks because front suspension drag links may corrode, potentially causing loss of steering.

    Product
    VOLVO — VOLVO VT, VNM, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V092000·2016-02-18

    Highland Ridge RV Recalls Trailers Due to Incorrect Weight Rating Labels

    Highland Ridge RV is recalling 2015-2016 travel and fifth wheel trailers because incorrect Gross Vehicle Weight Rating labels may allow overloading, increasing the risk of tire failure and crashes.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW ROAMER, HIGHLANDER, LIGHT, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V093000·2016-02-18

    Mercedes-Benz and Freightliner Sprinter Vans Recalled for Incorrect Tire Labels

    Daimler Vans USA is recalling 2015-2016 Sprinter vans because tire pressure labels list incorrect maximum load capacities, which could lead to axle or tire failure.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16106·2016-02-18

    Apple Recalls Travel Adapter Kits Due to Electric Shock Risk

    Apple is recalling approximately 814,000 travel adapter kits and plug adapters because the two-prong adapters can break and expose metal, posing an electric shock risk.

    Product
    AC adapter kits and plug adapters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16727·2016-02-18

    ENVE Recalls Bicycle Forks Due to Fall Hazard

    ENVE is recalling about 600 carbon fiber bicycle forks because the left leg can crack, posing a fall hazard. No injuries have been reported.

    Product
    Bicycle Forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16C003000·2016-02-18

    Evenflo Recalls Transitions 3-in-1 Booster Seats Due to Harness Defect

    Evenflo is recalling specific Transitions 3-in-1 Combination Booster Seats because the harness adjuster button may be within a child's reach, allowing them to loosen the harness and increasing injury risk in a crash.

    Product
    CHILD SEAT:HARNESS:STRAP/WEBBING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16107·2016-02-18

    Raynor Recalls Eurotech Lume Office Chairs Due to Fall Hazard

    Raynor Marketing is recalling about 1,200 Eurotech Lume office chairs because the seat can detach, posing a fall hazard. No injuries have been reported.

    Product
    Eurotech Lume office chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide