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.

46851–46875 of 73987

CriticalFDA (Food)·F-2001-2016·2016-09-07
General Mills Recalls Nature Valley Bars Due to Listeria Risk
General Mills is voluntarily recalling Nature Valley Protein Chewy Bars and Simple Nut Bars due to potential Listeria monocytogenes contamination from sunflower kernels.
Product
Nature Valley Protein Chewy Bars, Honey, Peanut & Almond with Pumpkin Seeds, Carton UPC 000-16000-47196, Case UPC 100-16000-47196, 5 bars/carton, 5-1.42 OZ (40 g)BARS, NET WT 7.1 OZ (201 g).
Category
Food
Distribution
5 states
CriticalFDA (Food)·F-2006-2016·2016-09-07
International Foodsource Recalls Raw Pistachios Due to Salmonella Risk
International Foodsource, LLC is recalling raw pistachios because FDA testing found Salmonella contamination.
Product
Sam International Bulk Raw Whole Pistachio 80% VP Net Wt. 30 lb Packaged in Boxes
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2675-2016·2016-09-07
Intuitive Surgical da Vinci EndoWrist Stapler 45 Recall for Field Failures
Intuitive Surgical is recalling da Vinci EndoWrist Stapler 45 instruments due to reported field failures involving shaft rotation interruptions and jaw opening issues.
Product
STAPLER,IS4000; Model number 470298; General and Plastic Surgery: The Intuitive Surgical da Vinci EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci Xi Surgical System (Model IS4000) for resection, transection…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-2034-2016·2016-09-07
Hampton Creek White Cake Mix Recalled for Salmonella Risk
Hampton Creek Foods is recalling JUST White Cake Mix because a positive test for Salmonella was found in the coconut milk powder used in its manufacturing.
Product
JUST White Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567 g); UPC 8 54829 00688 6. Ingredients: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin, reduced Iron…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2007-2016·2016-09-07
Raw Pistachio Kernels Recalled Due to Salmonella Contamination
International Foodsource LLC is recalling 9,756 bags of Valued Natural Raw Pistachio Kernels due to potential Salmonella contamination.
Product
Valued Natural Raw Pistachio Kernels Net Wt 5 oz. (141 g) International Foodsource LLC 52 Richboynton, Rd. Dover, NJ 07801 UPC 790429241428
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·16V646000·2016-09-07
Audi Recalls 2012-2013 A6 and A7 for Fuel Hose Leak Risk
Volkswagen Group of America is recalling 28,249 Audi A6 and A7 vehicles because a fuel hose may degrade and leak, increasing fire risk.
Product
AUDI — AUDI A7, A6
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-2013-2016·2016-09-07
Big Pig Bacon Seasoning Salt Recalled for E. coli O121 Contamination Risk
J&D's Down Home Enterprises is recalling Big Pig Original Bacon Flavored Seasoning Salt due to potential E. coli O121 contamination.
Product
Original Bacon Flavored Seasoning Salt, Big Pig brand, 16oz plastic jars, 3 jars per case. UPC 98300 00110
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2676-2016·2016-09-07
Intuitive Surgical Recalls da Vinci EndoWrist Stapler 30 Instruments
Intuitive Surgical is recalling 875 da Vinci EndoWrist Stapler 30 instruments due to reported field failures involving shaft rotation interruption or jaws not opening.
Product
STAPLER 30,IS4000; Model number 470430; General and Plastic Surgery: The Intuitive Surgical da Vinci EndoWrist Stapler 30 Instrument and Stapler 30 Reloads are intended to be used with the da Vinci Xi Surgical System (Model IS4000) for resection, transection and/or creation…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2677-2016·2016-09-07
Intuitive Surgical Recalls da Vinci EndoWrist Stapler 30 Instruments
Intuitive Surgical is recalling 875 da Vinci EndoWrist Stapler 30 instruments due to reported shaft rotation interruptions and jaw opening failures.
Product
CURVED-TIP STAPLER 30,IS4000; Model number 470530; General and Plastic Surgery: The Intuitive Surgical da Vinci EndoWrist Stapler 30 Instrument and Stapler 30 Reloads are intended to be used with the da Vinci Xi Surgical System (Model IS4000) for resection, transection…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V647000·2016-09-07
Volkswagen and Audi Recall 2015-2016 Models for Fuel Leak Fire Risk
Volkswagen is recalling 2015-2016 Golf, GTI, and Audi A3 vehicles because a faulty fuel pump may cause leaks that increase fire risk.
Product
VOLKSWAGEN — VOLKSWAGEN, AUDI GOLF, GTI, A3 CABRIOLET
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-2016-2016·2016-09-07
Hampton Creek Muffin Mix Recalled for Salmonella in Coconut Milk Powder
Hampton Creek Foods is recalling JUST Chocolate Chunk Muffin Mix because a positive test result for Salmonella was found in the coconut milk powder used in manufacturing.
Product
JUST Chocolate Chunk Muffin Mix; NET WT 20.8 oz. (1 lb 4.8 oz) 590 g); UPC 8 54829 00656 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2018-2016·2016-09-07
Hampton Creek Blueberry Muffin Mix Recalled for Salmonella Risk
Hampton Creek Foods is recalling JUST Blueberry Muffin Mix because a positive test for Salmonella was found in the coconut milk powder used to make it.
Product
JUST Blueberry Muffin Mix; NET WT 23.3 oz. (1 lb 7.3 oz) 660 g); UPC 8 54829 00685 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2035-2016·2016-09-07
Hampton Creek Cinnamon Roll Coffee Cake Mix Recalled for Salmonella
Hampton Creek Foods is recalling JUST Cinnamon Roll Coffee Cake Mix because a positive test for Salmonella was found in the coconut milk powder used in its manufacturing.
Product
JUST Cinnamon Roll Coffee Cake Mix; NET WT 26.9 oz. (1 lb 10.9 oz) 762 g); UPC 8 54829 00644 2. Ingredients: Cake Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2019-2016·2016-09-07
Hampton Creek Devil's Food Cake Mix Recalled for Salmonella
Hampton Creek Foods is recalling Devil's Food Cake Mix because a positive test found Salmonella in the coconut milk powder used in manufacturing.
Product
JUST Devil's Food Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567 g); UPC 8 54829 00643 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2017-2016·2016-09-07
Hampton Creek Recalls JUST Yellow Cake Mix Due to Salmonella Risk
Hampton Creek Foods is recalling JUST Yellow Cake Mix because a positive test for Salmonella was found in the coconut milk powder used to make it.
Product
JUST Yellow Cake Mix; NET WT 20 z. (1 lb 4oz) 567 g); UPC 8 54829 00642 8. Ingredients: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin, reduced Iron…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2692-2016·2016-09-07
Beckman Coulter Recalls UniCel DxH Slidemaker Stainer Due to Fire Risk
Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer because flammable liquids may contact electrical components, posing a fire hazard.
Product
UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Catalog No. 775222 UniCel DxH Slidemaker Stainer (DxH SMS) Instructions for Use (IFU) Part Number B26647AC The DxH Slidemaker Stainer is a fully automated slide preparation and staining device that aspirates a…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-2008-2016·2016-09-07
IFS Raw Shelled Pistachios Recalled for Potential Salmonella Contamination
International Foodsource LLC is recalling raw shelled pistachios due to potential Salmonella contamination found in FDA testing.
Product
IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. 3 lb. (1 kg) International Foodsource LLC 52 Richboynton Rd. Dover NJ 07801 UPC 790429243026
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2673-2016·2016-09-07
Nakanishi Diamond Coated Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 2,574 diamond coated tips and burs because the labeling failed to indicate they are single-use only, posing a cross-contamination risk.
Product
Diamond Coated Tips and Burs are accessories to the air powered Bone drill (VARIOSURG with and without light) The intended use of the tips is based on the parent device. For the VarioSurg, in addition to the scaling functions, diamond coated tips are used for socket lift, sinus…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2713-2016·2016-09-07
Cardinal Health Recalls Arterial Blood Gas Kits Missing Safety Clasp
Cardinal Health is recalling specific lots of 9025TRU Arterial Blood Gas Kits because they are missing a locking clasp component, posing a potential safety risk.
Product
The 9025TRU Arterial Blood Gas (ABG) Kit is used to obtain arterial blood sampling for pH, Blood Gas, Electrolyte and Metabolite Analysis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2709-2016·2016-09-07
Merge Cardio software recall due to incorrect patient data saving
Merge Healthcare is recalling Merge Cardio software versions 10.1 and 10.1.1 because reports may be saved to incorrect patient records.
Product
Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI. Image processing system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V645000·2016-09-07
Forest River Recalls 2017 Coachmen Viking Trailers Due to Roof Strut Defect
Forest River is recalling 2017 Coachmen Viking recreational trailers because a missing wire clip may allow the roof strut to detach, causing the roof to drop and increasing injury risk.
Product
COACHMEN — COACHMEN VIKING
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16T014000·2016-09-07
Tireco Recalls Milestar Tires with Incorrect Sidewall Markings
Tireco is recalling specific Milestar BS623 tires with incorrect sidewall markings that may lead to overloading and tire failure.
Product
TIRES:MARKINGS recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2691-2016·2016-09-07
Elekta Recalls HexaPOD evo RT Systems for Positioning Errors
Elekta is recalling 13 HexaPOD evo RT Systems because the treatment couch may not move fully to the correct 3D position, potentially leading to unrecognized positioning errors during radiotherapy.
Product
HexaPOD evo RT System Product Usage: The intended use of the device is the control of accurate patient positioning with assistance of a 3D Tracking System in a radiotherapy environment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2689-2016·2016-09-07
Mindray A7 Anesthesia Delivery System Recalled for Potential Oxygen Leak
Mindray is recalling 167 A7 Anesthesia Delivery Systems due to a potential leak on the back-up oxygen and air cylinder yokes.
Product
A7 Anesthesia Delivery System, a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. Part numbers 0632F-PA0000X (US domestic) and 0632B-00014 (international)
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16C007000·2016-09-07
Evenflo Recalls Evolve 3-in-1 Booster Seats Due to Harness Loosening Risk
Evenflo is recalling specific Evolve 3-in-1 Combination Booster Seats because children can access a button to loosen the harness, increasing injury risk in a crash.
Product
CHILD SEAT:HARNESS:STRAP/WEBBING recall
Category
Consumer Product
Distribution
Distributed nationwide