State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

61276–61300 of 74011

SevereFDA (Food)·F-0039-2014·2013-10-30
Chobani Greek Yogurt Recalled Due to Illness Reports and Swollen Packaging
Chobani is recalling specific Pineapple Greek Yogurt products due to reported illnesses and bloated packaging. Consumers should check Best By dates and stop using affected items.
Product
12/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Pineapple Fruit on the Bottom, 8-94700-01010-6; 6/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Pineapple on the Bottom-6 Value Pack, 8-94700-01038-0; 6/4/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Pineapple on the Bottom-4…
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·13V538000·2013-10-30
Freightliner Recalls 2013 Cascadia Trucks for Missing Axle Snap Rings
Daimler Trucks North America is recalling 2013 Freightliner Cascadia trucks because a missing axle snap ring could cause rear wheels to separate, increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0014-2014·2013-10-30
Chobani Greek Yogurt Recalled Due to Illness Reports and Swollen Packaging
Chobani is recalling specific lots of 0% Non-Fat Greek Yogurt Vanilla Blended because of reported illnesses and bloated packaging.
Product
12/6 oz. Chobani 0% Non-Fat Greek Yogurt Vanilla Blended, UPC 8-94700-01002-1; 6/16 oz. Chobani 0% Non-Fat Greek Yogurt Vanilla Blended, UPC 8-94700-01008-3; 6/32 oz. Chobani 0% Non-Fat Greek Yogurt Vanilla Blended, UPC 8-94700-01014-4; 6/4/6 oz. Chobani 0% Non-Fat Greek…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0023-2014·2013-10-30
Chobani Greek Yogurt Recalled Due to Illness Reports and Swollen Packaging
Chobani is recalling 74,295 cases of Strawberry Banana Blended Greek Yogurt nationwide due to reported illnesses and bloated packaging.
Product
12/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Strawberry Banana Blended, UPC 8-94700-01032-8; 6/4/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Strawberry Banana Blended, UPC 8-18290-01280-7
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0008-2014·2013-10-30
Vinco's Fem-Vite Recalled Due to Potential Salmonella Contamination
Vinco Inc. is recalling specific lots of Fem-Vite Women's Anti-Oxidant Formula because the soy ingredient may be contaminated with Salmonella.
Product
Vinco's Fem-Vite Women's Anti-Oxidant Formula, Dietary Supplement, 60 Tablets, distributed by Vinco, Inc., Evans City, PA
Category
Food
Distribution
Distributed nationwide
HighNHTSA·13V541000·2013-10-30
McLaren Recalls MP4-12C Vehicles for Wiper Motor Defect
McLaren is recalling 2012-2014 MP4-12C vehicles in six states because wiper motors may stop working in hot, humid weather, increasing crash risk.
Product
MCLAREN — MCLAREN MP4-12C SPIDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·13V536000·2013-10-30
Thomas Built Minotour School Bus Seat Barrier Recall
Daimler Trucks North America is recalling 2013 Thomas Built Minotour school buses due to incorrect seat barrier installation that may increase injury risk in a crash.
Product
THOMAS BUILT — THOMAS BUILT MINOTOUR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0048-2014·2013-10-30
Abbott Medical Optics Recalls STAR Excimer Laser Systems Due to Component Failure
Abbott Medical Optics is recalling STAR Excimer Laser Systems due to a thyristor component failure that affects the lamp and illumination system.
Product
STAR Excimer Laser System with Variable Spot Scanning, Model: STAR S4, Catalog Number: 0030-4077, Product is manufactured and distributed by AMO Manufacturing USA, LLC, Milpitas, CA The STAR Excimer Laser Systems are indicated for laser assisted in situ keratomileusis…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·13V537000·2013-10-30
Thomas Built Buses Recall 2012-2014 Models for Missing Seat U-Bolts
Daimler Trucks North America is recalling 328 Thomas Built Saf-T-Liner school buses because a U-bolt may be missing, which could cause seats to detach in a crash.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER EFX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0058-2014·2013-10-30
Integra Licox Brain Tissue Oxygen Monitoring Kits Recalled for Defective Hex Wrench
Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring Kits because some contain a hex wrench that may not loosen the set screw on the drill bit.
Product
Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Probe Kit REF IM3.SR Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive Plainsboro…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0049-2014·2013-10-30
Abbott STAR Excimer Laser Systems Recalled for Thyristor Component Failure
Abbott Medical Optics is recalling STAR Excimer Laser Systems due to a thyristor failure on the AC Power Distribution PCB that affects the lamp and illumination system.
Product
STAR Excimer Laser System, Model STAR S4 IR, Catalog Number: 0030-4864, Product is manufactured and distributed by AMO Manufacturing USA, LLC Milpitas, CA The STAR Excimer Laser Systems are indicated for laser assisted in situ keratomileusis (LASIK), photorefractive…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0055-2014·2013-10-30
Integra Licox Brain Tissue Oxygen Monitoring Kits Recalled for Defective Hex Wrench
Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring kits because a hex wrench may fail to loosen the set screw on the drill bit.
Product
Integra Licox Brain Tissue Oxygen Monitoring; 1 x Dual Lumen Introducer Kit REF IP2; Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive Plainsboro, NJ…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·13V539000·2013-10-30
Thomas Built Buses Recalls 2014 Saf-T-Liner C2 School Buses for Seat Rivets
Daimler Trucks North America is recalling 73 model year 2014 Saf-T-Liner C2 school buses because improperly seated seat track rivets may prevent seat belts from working correctly in a crash.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·14009·2013-10-30
HeathCo Recalls Motion-Activated Outdoor Lights Due to Electrical Shock Hazard
HeathCo is recalling about 223,000 motion-activated outdoor lights in the U.S. and Canada because the internal wiring can energize the fixture surface, posing an electrical shock hazard.
Product
Motion-Activated Outdoor Lights
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0006-2014·2013-10-30
Vinco's OsteoSheath Calcium Supplement Recalled for Potential Salmonella Contamination
Vinco Inc. is recalling certain lots of OsteoSheath Enhanced Bone Support calcium supplements because the soy ingredient used in manufacturing was potentially contaminated with Salmonella.
Product
Vinco's OsteoSheath Enhanced Bone Support, Calcium Supplement, 90 Tablets, distributed by Vinco, Inc., Evans City, PA;
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0028-2014·2013-10-30
Becton Dickinson Recalls BBL MGIT Mycobacteria Tubes Due to Barcode Error
Becton Dickinson is recalling 187,000 BBL MGIT Mycobacteria Growth Indicator Tubes because incorrect barcodes may cause false negative test results.
Product
BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube, part # 245122, packaged in 100 ct cartons and labeled in part Product Usage: The Mycobacteria Growth Indicator Tube supplemented with Bactec MGIT Growth Supplement and BBL MGIT PANTA antibiotic mixture is intended for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0007-2014·2013-10-30
Vinco's OsteoSheath 4 Calcium Supplement Recalled for Salmonella Risk
Vinco Inc. is recalling certain lots of OsteoSheath 4 calcium supplements because the soy ingredient used was potentially contaminated with Salmonella.
Product
Vinco's OsteoSheath 4 Enhanced Bone Support, Calcium Supplement, 120 Tablets, distributed by Vinco, Inc., Evans City, PA
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0047-2014·2013-10-30
Abbott Recalls STAR Excimer Laser Systems Due to Power Component Failure
Abbott Medical Optics is recalling STAR Excimer Laser Systems because a power component failure can cause the lamp and illumination system to malfunction.
Product
STAR ActiveTrak Excimer Laser System, Model: STAR S3, Catalog Number: 0030-2450, Product is manufactured and distributed by AMO Manufacturing USA, LLC, Milpitas, CA The STAR Excimer Laser Systems are indicated for laser assisted in situ keratomileusis (LASIK), photorefractive…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0060-2014·2013-10-30
Integra Licox Brain Tissue Oxygen Monitoring Kit Recall for Hex Wrench Defect
Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring Kits because a hex wrench may fail to loosen the set screw on the drill bit.
Product
Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Introducer Kit REF IM2_EU Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive Plainsboro…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0076-2014·2013-10-30
Dannon Oikos Blueberry Yogurt Recalled for Incorrect Blackberry Labeling
Dannon is recalling Oikos Blueberry Greek Yogurt because the cups are incorrectly labeled as blackberry flavor, failing to declare the allergen carmine.
Product
DANNON OIKOS Fruit on the Bottom GREEK NONFAT YOGURT BLUEBERRY 0% FAT
Category
Food
Distribution
Distributed nationwide
HighNHTSA·13V523000·2013-10-30
Ford Recalls 2012-2014 Focus Electric Vehicles for Software Defect
Ford is recalling 2012-2014 Focus Electric vehicles because a software problem may cause a stall-like condition, increasing crash risk.
Product
FORD — FORD FOCUS ELECTRIC
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·14008·2013-10-30
Southern Telecom Recalls A/C Adaptors for Polaroid Internet Tablets
Southern Telecom is recalling A/C adaptors for Polaroid PMID 709 Internet Tablets due to a fire hazard. The adaptors can overheat, posing a risk of fire.
Product
A/C Adaptor (charger) included with Polaroid PMID 709 Internet Tablets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0051-2014·2013-10-30
Synergetics 25 Gauge Soft Tip Cannula Recall Due to Gauge Mislabeling
Synergetics Inc is recalling 25 gauge Soft Tip Cannulas because some units are co-mingled with 23 gauge cannulas but labeled as 25 gauge.
Product
Synergetics 25 gauge Soft Tip Cannula, packaged in 6 units per box. Catalog number: 30.08.25. Single-use 25 gauge cannula used in vitreoretinal surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0034-2014·2013-10-30
GE Healthcare Recalls Centricity Cardio Imaging 5.0 Software
GE Healthcare is recalling Centricity Cardio Imaging 5.0 software due to a potential image labeling error in the Image Viewer that may affect diagnostic interpretation.
Product
Centricity Cardio Imaging 5.0 is a software only Picture Archiving and Communication System (PACS). Product Usage: It will be sold as a software only device to operate on general purpose computing hardware. Centricity Cardio Imaging receives medical images and other…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0044-2014·2013-10-30
Advanced Sterilization Products Recalls STERRAD 100NX Cassettes Due to Leak Indicator Issue
Advanced Sterilization Products is recalling STERRAD 100NX Cassettes because the leak indicator is effective for only 12 months, not the labeled 15 months.
Product
STERRAD 100NX Cassettes The STERRAD Sterilization System is a low temperature general purpose sterilizer used to sterilize heat and moisture sensitive reusable medical devices.
Category
Medical Device
Distribution
Distributed nationwide