The Recall Desk

State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57726–57750 of 74005

  • ModerateFDA (Devices)·Z-2104-2014·2014-07-30

    Terumo Recalls Three-stage Venous Return Cannulae Due to Loose Fiber Particulate

    Terumo Cardiovascular Systems is recalling specific lots of Three-stage Venous Return Cannulae because in-process inspections found loose fiber particulate exceeding specifications.

    Product
    Terumo Three-stage Venous Return Cannulae 28 Fr with 3/8" flare, 30 Fr with 3/8" connector and 30 Fr with 3/8" flare. Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2210-2014·2014-07-30

    Kraft Recalls Knudsen, Breakstone's, and Other Cottage Cheese Brands

    Kraft Foods is voluntarily recalling multiple cottage cheese brands due to ingredients not being stored at proper temperatures.

    Product
    Cottage Doubles - cottage cheese, 2% milkfat, with peach topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2207-2014·2014-07-30

    Kraft Recalls Cottage Cheese Due to Temperature Storage Issues

    Kraft Foods is voluntarily recalling Knudsen, Breakstone's, Simply Kraft, and Daily Chef cottage cheese because ingredients were not stored at proper temperatures.

    Product
    Fat free cottage cheese sold under the Knudsen or Kraft brand and packaged in a plastic container with a net weight of 16 oz. (1 lb.) 453 g, a plastic container with a net weight of 24 oz. (1.5 lb.) 680 g, or a plastic container with a net weight of 32 oz. (2 lb.) 907 g.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2095-2014·2014-07-30

    Terumo Recalls Sarns Aortic Arch Cannulas Due to Loose Fiber Particulate

    Terumo CVS is recalling 120 units of Sarns Flexible Aortic Arch Cannulas because in-process inspections found loose fiber particulate exceeding specifications.

    Product
    Sarns Flexible Aortic Arch Cannula 8.0mm with luer, 3/8" connector Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2213-2014·2014-07-30

    Kraft Recalls Knudsen and Other Cottage Cheese Due to Storage Issues

    Kraft Foods is voluntarily recalling multiple cottage cheese brands due to ingredients not being stored at proper temperatures.

    Product
    Cottage Doubles - cottage cheese, 2% milkfat, with blueberry topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2093-2014·2014-07-30

    Salter Labs Recalls Oxygen Masks Due to Incorrect Labeling

    Salter Labs is recalling 584 units of Model No. 8120-7 oxygen masks because the insert label incorrectly identifies the device as a non-rebreather instead of a partial rebreather.

    Product
    Oxygen Mask, Model No. 8120-7 Product Usage: Oxygen Mask, High Concentration partial rebreather, with 7 foot (2.1 m) supply tube, Elastic Strap Fixation, Single patient use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2212-2014·2014-07-30

    Kraft Recalls Knudsen and Other Cottage Cheese Brands Due to Storage Issues

    Kraft Foods is voluntarily recalling multiple cottage cheese brands produced in Tulare, CA, because ingredients were not stored at proper temperatures.

    Product
    Cottage Doubles - cottage cheese, 2% milkfat, with pineapple topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2101-2014·2014-07-30

    Terumo Recalls Sarns Venoatrial Cannulae Due to Loose Fiber Particulate

    Terumo CVS is recalling 3,040 Sarns Venoatrial Cannulae units because in-process inspections found loose fiber particulate exceeding specifications.

    Product
    Sarns Venoatrial Cannulae 36/46 Fr with 1/2" flare or connector Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use. The Venous Return Cannula…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2103-2014·2014-07-30

    Terumo TenderFlow Pediatric Venous Cannulae Recalled for Loose Fiber Particulate

    Terumo CVS is recalling specific lots of TenderFlow Pediatric Venous Cannulae due to loose fiber particulate exceeding specifications found during inspection.

    Product
    Terumo TenderFlow Pediatric Venous Cannulae, 8, 10, 12, 14, 16, 18, 20, 22 & 24 Fr angled & straight tip, 1/4" & 3/8" flare, Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2209-2014·2014-07-30

    Kraft Recalls Cottage Cheese Due to Temperature Storage Violations

    Kraft Foods is voluntarily recalling multiple brands of cottage cheese because ingredients were not stored at proper temperatures, creating a potential safety risk.

    Product
    Cottage cheese, 4% milkfat, sold under the Daily Chef, Knudsen, or Kraft brand and packaged in a plastic container with a net weight of 8 oz. (227 g), a plastic container with a net weight of 16 oz. (1 lb.) 453 g, a plastic container with a net weight of 24 oz. (1.5 lb.) 680 g…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2208-2014·2014-07-30

    Kraft Recalls Cottage Cheese Due to Improper Ingredient Storage

    Kraft Foods is voluntarily recalling cottage cheese sold under Breakstone's, Daily Chef, Knudsen, and Kraft brands because ingredients were not stored at proper temperatures.

    Product
    Low fat cottage cheese, 2% milkfat, sold under the Breakstone's brand, Daily Chef brand, Knudsen brand, or Kraft brand packaged in a tray of 4 plastic containers each with a net weight of 4 oz. (113 g), a tray of 8 plastic containers each with a net weight of 4 oz. (113 g), a…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2214-2014·2014-07-30

    Kraft Recalls Knudsen and Other Cottage Cheese Due to Temperature Storage Issues

    Kraft Foods is voluntarily recalling multiple cottage cheese brands produced in Tulare, CA, because ingredients were not stored at proper temperatures.

    Product
    Cottage Doubles - cottage cheese, 2% milkfat, with raspberry topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1444-2014·2014-07-30

    X-Gen Recalls Clonidine HCl Injection Due to Labeling Error

    X-Gen Pharmaceuticals is recalling Clonidine HCl Injection vials because the side label incorrectly states the drug strength.

    Product
    CLONIDINE — CLONIDINE (CLONIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1445-2014·2014-07-30

    Sandoz Recalls Orphenadrine Citrate Tablets for Dissolution Failures

    Sandoz Inc. is recalling Orphenadrine Citrate Extended Release Tablets because they failed dissolution specifications during stability testing.

    Product
    ORPHENADRINE CITRATE — ORPHENADRINE CITRATE (ORPHENADRINE CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1452-2014·2014-07-30

    Estee Lauder Recalls DENBLAN Toothpaste Due to Stability Data Issues

    Estee Lauder Inc is recalling 3,791 tubes of DENBLAN Anticavity Fluoride Toothpaste because stability data does not support the product's expiry date.

    Product
    DENBLAN Anticavity Fluoride Toothpaste, Whitening formula, sodium monofluorophosphate 0.76%, 2.6 oz/75 mL tube, Laboratories Darphin, Dist, Paris France
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E051000·2014-07-29

    Cummins Fleetguard Fuel Filter Recall for Engine Stalling Risk

    Cummins is recalling specific Fleetguard UFF-XT fuel filters installed on ISB and ISL engines because the filter shell may separate, causing the engine to stall without warning and increasing crash risk.

    Product
    FUEL SYSTEM, DIESEL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V460000·2014-07-29

    GM Recalls 2009-2010 Chevrolet Aveo and Pontiac G3 for Brake Defect

    General Motors is recalling 2009-2010 Chevrolet Aveo and 2009 Pontiac G3 vehicles because brake fluid may corrode ABS valves, potentially reducing braking performance.

    Product
    CHEVROLET — CHEVROLET, PONTIAC AVEO, G3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E050000·2014-07-29

    Dana Commercial Vehicle Driveshaft Recall for Welded Bond Failure

    Dana is recalling commercial vehicle lightweight driveshafts where the welded bond may fail, potentially causing loss of torque to the rear wheels.

    Product
    POWER TRAIN:DRIVELINE:DRIVESHAFT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14242·2014-07-29

    Philips Recalls Lightolier Glass Lenses Due to Laceration Hazard

    Philips Lighting is recalling Lightolier AF4SY decorative glass lenses because they can shatter and cause cuts. Consumers should remove the lenses and contact Philips for a free replacement.

    Product
    Philips "Lightolier" brand AF4SY Decorative Glass Lens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V457000·2014-07-28

    Porsche Recalls 2015 918 Spyder for Rear Axle Control Arm Defect

    Porsche is recalling 2015 918 Spyder vehicles because rear-axle control arms may break, potentially causing loss of vehicle control and increasing crash risk.

    Product
    PORSCHE — PORSCHE 918 SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V459000·2014-07-28

    Gillig Recalls 2013-2014 Low Floor Buses for Brake Valve Defect

    Gillig is recalling 252 Low Floor transit buses from 2013-2014 because they may lack a rear brake quick release valve, potentially causing rear wheel lockup.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E049000·2014-07-28

    Delphi Recalls Fuel Pump Modules for 2005-2010 Honda Odyssey Vehicles

    Delphi is recalling replacement fuel pump modules for 2005-2010 Honda Odysseys that may display incorrect fuel levels, increasing the risk of stalling and crashes.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·049-2014·2014-07-26

    Puritan Foods Recalls Raw Turkey Breasts for Undeclared Milk Allergen

    Puritan Foods Co. is recalling raw boneless turkey breasts because the product contains milk, a known allergen, that is not declared on the label.

    Product
    Puritan Foods Co., Inc. — Massachusetts Firm Recalls Raw Boneless Turkey Breasts Due To Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide