The Recall Desk

State

US Virgin Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47301–47325 of 73987

  • ModerateFDA (Devices)·Z-2340-2016·2016-08-10

    Zimmer Air Dermatome II Width Plate Recalled for Surface Coating Defects

    Zimmer Surgical Inc is recalling 110 units of the Air Dermatome II Width Plate because the surface coating is blistering, peeling, and discoloring after use.

    Product
    Zimmer¿ Air Dermatome II Width Plate, 4 inch. Part #00-8851-204-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2314-2016·2016-08-10

    Medtronic Navigation Recalls StealthStation Software Applications

    Medtronic Navigation is conducting a voluntary field action for StealthStation software applications affected by Neurologica BodyTom/CereTom floor-based scanners.

    Product
    FrameLink. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or percutaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2315-2016·2016-08-10

    Medtronic Navigation Recalls S7 MACH FrameLink Software Applications

    Medtronic Navigation is conducting a voluntary field action for S7 MACH FrameLink software applications affected by Neurologica BodyTom/CereTom floor-based scanners.

    Product
    S7 MACH FrameLink. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or percutaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2309-2016·2016-08-10

    Beckman Coulter AU680 Chemistry Analyzers Recalled for Leaking C Cups

    Beckman Coulter is recalling AU680 Chemistry Analyzers because leaking and cracked C cups can cause coolant to leak onto circuit boards, resulting in short-circuits and instrument stop mode.

    Product
    AU680 Chemistry Analyzers, Reference No. B04779 The AU series are automated, clinical chemistry analyzers that measure analytes in patient samples (serum, plasma, urine, CSF) in combination with appropriate reagents, calibrators, quality, control (QC) materials, and other…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1453-2016·2016-08-10

    Teva Recalls Children's Qnasl Nasal Aerosol for Content Uniformity Failure

    Teva North America is recalling Children's Qnasl nasal aerosol canisters due to failed spray content uniformity tests. The FDA classified this as a Class III recall.

    Product
    Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol, 40 mcg per spray, 60 Metered Sprays per canister, 4.9g Net Contents, Rx only; Professional Sample; Manufactured for Teva Respiratory, LLC, Horsham, PA 19044; By: 3M Drug Delivery Systems, Northridge, CA…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2333-2016·2016-08-10

    C.R. Bard Recalls SureStep Urine Collection System for Labeling Issues

    C.R. Bard is recalling 530 SureStep urine collection systems due to a labeling problem. The recall is voluntary and nationwide.

    Product
    SureStep Tray, with Add-a-Foley, COMPLETE CARE, Drainage Bag, and STATLOCK Stabilization The product is a urine collection system that includes a STATLOCK Foley Stabilization Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2311-2016·2016-08-10

    Branan Medical Recalls AmediCheck Instant Test Cups Due to Packaging Error

    Branan Medical is recalling AmediCheck Instant Test Cups because they may erroneously contain 12-panel cups due to a packaging error.

    Product
    AmediCheck Instant Test Cup, Part No. C-C0501A-3A Product Usage: The AmediCheck Instant Test Cup is an in vitro diagnostic test for the rapid detection of the following drugs in human urine. Drug Analyte Cut off Device Code Marijuana THC 50 ng/mL THC Cocaine Benzoylecgonine…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16239·2016-08-09

    Kohler Recalls Portable Generators Due to Electrical Shock Hazard

    Kohler Power Systems is recalling specific portable generator models due to a wiring error that creates an electrical shock risk. Consumers should stop using these units and contact Kohler for a free repair.

    Product
    Kohler portable generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16240·2016-08-09

    Brown Jordan Recalls Swivel Patio Chairs Due to Fall Hazard

    Brown Jordan Services is recalling Hampton Bay swivel patio chairs because the base can break, posing a fall hazard. Consumers should stop using the chairs and contact the company for a free repair kit.

    Product
    Swivel Dining and Lounge Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V586000·2016-08-08

    KME Predator Fire Apparatus Recalled for Touchscreen Malfunctions

    KME is recalling specific Predator fire apparatus vehicles because touchscreen malfunctions may cause accessories to turn on or off unexpectedly, increasing crash risk.

    Product
    KME — KME PREDATOR TRACTOR AERIAL, 7600 TANKER, PREDATOR PANTHER RESCUE, PREDATOR PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V584000·2016-08-05

    Eldorado E-Z Rider II Transit Bus Recall for Tire Clearance Issue

    Eldorado is recalling 2016 E-Z Rider II transit buses because front steel rims may allow tires to contact tie-rods, risking sudden air loss and crashes.

    Product
    ELDORADO — ELDORADO E-Z RIDER II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E068000·2016-08-05

    WSB Recalls WSB777 Half Helmets for Insufficient Crash Protection

    WSB Inc is recalling WSB777 half helmets manufactured in May 2015 because they may lack required labeling and fail to provide adequate head protection in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V585000·2016-08-05

    Pierce Fire Trucks Recalled for Transmission Shift Unit Defect

    Pierce Manufacturing is recalling 2015-2016 fire trucks because a damaged transmission component may prevent operators from switching power output to the water pump.

    Product
    PIERCE — PIERCE SABER, VELOCITY, DASH CF, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16766·2016-08-04

    Cinmar Recalls Magnetic Travel Maps Due to Magnet Ingestion Risk

    Cinmar is recalling World Magnetic Travel Maps sold at Frontgate because the included magnets pose a serious ingestion hazard to children.

    Product
    Magnetic travel maps with magnets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V583000·2016-08-04

    Smeal Fire Trucks Recalled for Transmission Shift Unit Defect

    Smeal is recalling 88 model year 2015-2016 Aerial and Pumper fire trucks because a damaged transmission component may prevent operators from switching power output, potentially hindering fire suppression.

    Product
    SMEAL — SMEAL AERIAL FIRE APPARATUS, AERIAL, PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V581000·2016-08-04

    Ferrara Fire Trucks Recalled for Transmission Shift Unit Defect

    Ferrara is recalling 2015-2016 fire trucks because a damaged transmission component may prevent operators from switching power output, potentially disabling water pumps.

    Product
    FERRARA — FERRARA INFERNO, IGNITER, CINDER, INTRUDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16765·2016-08-04

    John Deere Recalls Lawn Tractors Due to Laceration Hazard

    John Deere is recalling specific lawn and garden tractors because a safety system failure can cause laceration injuries to bystanders.

    Product
    Lawn and garden tractors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V582000·2016-08-04

    GM Recalls 2013 Chevrolet Equinox and GMC Terrain for Wiper Defect

    General Motors is recalling 2013 Chevrolet Equinox and GMC Terrain vehicles because windshield wiper ball joints may corrode, potentially rendering wipers inoperative and reducing visibility.

    Product
    GMC — GMC, CHEVROLET TERRAIN, EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1815-2016·2016-08-03

    CRF Frozen Foods Recalls Multiple Brands of Frozen Onions for Listeria Risk

    CRF Frozen Foods is recalling various brands of frozen chopped and diced onions due to potential Listeria monocytogenes contamination. The recall covers products distributed in the US, Canada, and Japan.

    Product
    Organic Chopped Onions, Brand Bybee Foods, Net Wt 45 lb, UPC R02303 Organic Diced Onions, Brand Columbia River Organics, Net Wt 10 oz, UPC 5711000116 Diced Onions, Brand Northwest Grower's Select, Net Wt 45 lb, UPC 19190 Pearl Onions, Brand Northwest Growers Select, Net…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1799-2016·2016-08-03

    CRF Frozen Foods Recalls Organic Sweet Cherries for Listeria Risk

    CRF Frozen Foods is recalling Columbia River Organics Organic Sweet Cherries due to potential Listeria monocytogenes contamination.

    Product
    Organic Sweet Cherries, brand Columbia River Organics, Net Wt 10 oz, UPC 5711000127
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1816-2016·2016-08-03

    CRF Frozen Foods Recalls Frozen Peas Due to Listeria Risk

    CRF Frozen Foods is recalling various brands of frozen peas nationwide and in Canada and Japan due to potential Listeria monocytogenes contamination.

    Product
    Green Peas, Brand Bybee's Best, Net Wt 20 lb, UPC 4635800011 Green Peas, Brand Byee Foods, Net Wt 50 lb, UPC 155000007785CR Organic Sweet Baby Peas, Brand Bybee Foods, Net Wt 5 lb, UPC 5711000145 Organic Petite Peas, Brand Columbia River Organics, Net Wt 10 oz, UPC…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1783-2016·2016-08-03

    CRF Frozen Foods Recalls Mixed Vegetables for Listeria Risk

    CRF Frozen Foods is recalling multiple brands of frozen mixed vegetables due to potential Listeria monocytogenes contamination. The products were distributed in the US, Canada, and Japan.

    Product
    Big House Blend, brand Bybee's, frozen, net wt. 30lb. UPC AZ#85 Best Mixed Vegetables, brand Bybee's, frozen, net wt. 20lb. UPC 4635800014 California Blend, brand Chef Maxwell, frozen, net wt. 20lb. UPC 063027 Raw Mixed Vegetables, brand Chef Maxwell, frozen, net wt.…
    Category
    Food
    Distribution
    Distributed nationwide