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.

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.

50076–50100 of 73995

  • HighCPSC·16108·2016-02-18

    BYA Sports Recalls Skyline Backyard Zipline Kits Due to Fall Hazard

    BYA Sports is recalling Skyline backyard zipline kits because a cable crimp can fail, posing a fall hazard. Consumers should stop using the kits and contact the company for a free replacement.

    Product
    Bring Your Adventure Sports (BYA) Skyline Zipline Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16105·2016-02-18

    Boa Recalls Snowboard Boots with M3v2 Reels Due to Fall Hazard

    Boa is recalling snowboard boots with M3v2 secondary reels because the mechanism can get stuck, loosening the fit and posing a fall hazard. No injuries have been reported.

    Product
    Snowboard Boots with Boa Secondary Reels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16728·2016-02-18

    J. Crew Recalls Girls' Puffer Coats Due to Choking Hazard

    J. Crew is recalling specific girls' puffer coats because front buttons can detach, posing a choking hazard to young children. No injuries have been reported.

    Product
    Girls' Crewcuts puffer coats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V091000·2016-02-18

    Navistar Recalls 2016-2017 IC CE School Buses for Hood Strap Defect

    Navistar is recalling 2016-2017 IC CE school buses because hood straps may elongate, allowing the hood to open unexpectedly during braking and obstructing the driver's vision.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V097000·2016-02-17

    Volvo Recalls 2016-2017 Trucks for Steering Shaft Separation Risk

    Volvo is recalling 2016-2017 VNL, VNX, and VNM trucks because a missing roll pin or loose bolt may cause the steering shaft to separate, resulting in a loss of steering.

    Product
    VOLVO — VOLVO VNX, VNM, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16102·2016-02-17

    Goodman Recalls Air Conditioning Units Due to Fire and Burn Hazards

    Goodman Company is expanding a recall for specific air conditioning and heating units because their power cords can overheat, posing fire and burn risks.

    Product
    Packaged Terminal Air Conditioner/Heat Pumps (PTAC) and Room Air Conditioners (RAC)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0767-2016·2016-02-17

    Mevion S250 Radiation Therapy System Recalled for Positioning Belt Slippage

    Mevion Medical Systems is recalling four MEVION S250 Radiation Therapy Systems because the treatment table positioning belt can slip, causing patient setup deviations.

    Product
    MEVION S250 Radiation therapy system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0760-2016·2016-02-17

    C.R. Bard Recalls Arctic Sun 5000 and 2000 Temperature Monitors

    C.R. Bard is recalling Arctic Sun 5000 and 2000 devices because a simulator key could be connected to the patient cable, resulting in improper temperature therapy.

    Product
    Arctic Sun 5000 and Arctic Sun 2000; Intended for monitoring and controlling patient temperatures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0793-2016·2016-02-17

    Smith & Nephew BEAVER Blade 4.0mm Recalled for Fracture Risk

    Smith & Nephew is recalling BEAVER Blade 4.0mm orthopedic instruments because they may fracture during hip arthroscopy procedures.

    Product
    Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic surgical instrument used in hip arthroscopy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0375-2016·2016-02-17

    Kraft Singles White American Recalled for Potential Choking Hazard

    Kraft Heinz is recalling Kraft Singles White American cheese slices because packaging film may remain on the slice, posing a choking risk.

    Product
    Kraft Singles White American singles packaged in a blue box with white lettering.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0376-2016·2016-02-17

    Kraft Singles Deli Deluxe American Slices Recalled for Choking Hazard

    Kraft Heinz is recalling specific lots of Kraft Singles Deli Deluxe American Slices because packaging film may remain on the cheese, posing a choking risk.

    Product
    Kraft Singles Deli Deluxe American Slices packaged in a blue box with white lettering.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0688-2016·2016-02-17

    Moog Recalls Curlin Infusion Pumps Due to Calibration Defect

    Moog is recalling specific Curlin infusion pumps because calibration errors may cause them to deliver medication faster than programmed.

    Product
    Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-therapy and PainSmart pumps. Curlin 4000, catalog number 340; Curlin 6000, 6000 CMS, and PainSmart IOD, catalog number 360; and Curlin Pump Calibration Set…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0374-2016·2016-02-17

    Kraft Singles American Recalled for Potential Choking Hazard

    The Kraft Heinz Company is recalling Kraft Singles American cheese slices because thin strips of packaging film may remain on the slices, posing a potential choking hazard.

    Product
    Kraft Singles American packaged in a blue box with white lettering.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0787-2016·2016-02-17

    DePuy SIGMA HP MBT Non-Keel Punch Knee Instrument Recalled

    DePuy Orthopaedics is recalling 351 SIGMA HP MBT Non-Keel Punch Knee Instruments due to a design defect that may cause surgical complications.

    Product
    SIGMA HP MBT Non-Keel Punch Knee Instrument. Designed to be used as an option in stabilizing the tibial trial during trial reduction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V090000·2016-02-17

    Navistar Recalls 2016 IC CE Buses for Hood Strap Defect

    Navistar is recalling 104 model year 2016 IC CE commercial buses because hood straps may elongate, causing the hood to open unexpectedly during braking and obstructing the driver's vision.

    Product
    IC BUS — IC BUS CE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0768-2016·2016-02-17

    GE Healthcare Optima XR220amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 2,389 Optima XR220amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.

    Product
    GE Healthcare, Optima XR220amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-0565-2016·2016-02-17

    Celestial Seasonings Roastaroma Herbal Tea Recalled for Gluten Mislabeling

    Hain Celestial is recalling Roastaroma Herbal Tea because some packages are labeled 'Gluten Free' but contain barley.

    Product
    Celestial Seasonings Roastaroma Herbal Tea Lot code: Best Before 20DEC17 Pack size: 6 retail units (20 count)/ per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0769-2016·2016-02-17

    GE Brivo XR285amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 126 Brivo XR285amx mobile radiographic systems worldwide because a safety latch mechanism may fail, posing a risk of bodily harm.

    Product
    GE Healthcare, Brivo XR285amx Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighCPSC·16103·2016-02-17

    Michaels Recalls Artificial Poinsettias Due to Mold Exposure Risk

    Michaels is recalling Ashland artificial poinsettia stems and bushes because mold may be present, posing a risk of respiratory or other infections.

    Product
    Ashland Poinsettia Stems and Bushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0770-2016·2016-02-17

    GE Healthcare Optima XR200amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 895 Optima XR200amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.

    Product
    GE Healthcare, Optima XR200amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighNHTSA·16V089000·2016-02-17

    Keystone Recalls 2016 Sprinter RVs Due to Falling Television Risk

    Keystone is recalling 2016 Sprinter recreational vehicles because a wall-mounted television may break off, posing an injury risk to occupants.

    Product
    KEYSTONE — KEYSTONE SPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0655-2016·2016-02-17

    Fagron Recalls SyrSpend SF Grape Flavor Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF Grape Flavor suspending base due to the presence of yeast. The recall affects 148 bottles distributed nationwide.

    Product
    SyrSpend SF, Suspending Base, Grape Flavored, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 4 L bottle, Manufactured by Fagron Inc., St. Paul, MN 55120…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·16104·2016-02-17

    Michaels Recalls Ashland Holiday Paper Boxes Due to Mold Risk

    Michaels is recalling Ashland holiday paper boxes because mold may be present, posing a risk of respiratory or other infections for consumers with compromised immune systems or mold allergies.

    Product
    Ashland® holiday paper boxes
    Category
    Consumer Product
    Distribution
    Distributed nationwide