State

US Virgin Islands product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28976–29000 of 73774

ModerateFDA (Devices)·Z-1930-2020·2020-05-20
Ortho-Clinical Diagnostics Recalls VITROS CKMB Slides Due to Incorrect Instructions
Ortho-Clinical Diagnostics is recalling VITROS CKMB Slides because Spanish and Swedish instructions incorrectly state the assay can be tested with plasma, which could result in biased results.
Product
VITROS Chemistry Products CKMB Slides, Creatine Kinase MB, Product Code 805 8232-300 slides, UDI Number 10758750004294 - Product Usage: The VITROS Chemistry Product Slides are used to measure creatine kinase MB (CK-MB) activity in serum which used to be ordered to detect…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2005-2020·2020-05-20
Genicon EZee Specimen Retrieval Bag Recall for Labeling Clarity
Genicon is recalling 1,550 units of the EZee Single Use Specimen Retrieval Bag to provide updated labeling instructions for multiple specimen retrieval.
Product
Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: This device is disposable and is packaged and sterilized for single use only. The bag may be used for multiple specimen retraction.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1949-2020·2020-05-20
Cardiac Assist Recalls TandemHeart Kits Due to Assembly Error
Cardiac Assist, Inc. is recalling five TandemHeart pump kits because an assembly error may prevent the device from priming.
Product
TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A15, Product: 5710-6215 - Product Usage: provides temporary extracorporeal circulatory system support with the unique ability to locally deliver an anticoagulant through the infusion system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1931-2020·2020-05-20
Ortho-Clinical Diagnostics Recalls VITROS CKMB Slides Due to Incorrect Instructions
Ortho-Clinical Diagnostics is recalling VITROS CKMB Slides because Spanish and Swedish instructions incorrectly state the assay can be tested with plasma, which could result in biased results.
Product
VITROS Chemistry Products CKMB Slides, Creatine Kinase MB, Product Code 8001133-90 slides, UDI Number 10758750004201 - Product Usage: The VITROS Chemistry Product Slides are used to measure creatine kinase MB (CK-MB) activity in serum which used to be ordered to detect…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1941-2020·2020-05-20
Medtronic Recalls Vertex Select Multi Axial Screws Due to Length Discrepancy
Medtronic is recalling 83 Vertex Select Multi Axial Screws because the product length is shorter than labeled. The recall covers units distributed in California and Michigan.
Product
VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1267-2020·2020-05-20
ChapStick Total Hydration Moisture Tint Recalled for Packaging Separation
Glaxosmithkline is recalling ChapStick Total Hydration Moisture Tint Very Berry due to observed separation in the secondary packaging.
Product
CHAPSTICK TOTAL HYDRATION MOISTURE TINT VERY BERRY — CHAPSTICK TOTAL HYDRATION MOISTURE TINT VERY BERRY (ZINC OXIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1268-2020·2020-05-20
ChapStick Total Hydration Moisture Tint Recalled for Packaging Separation
Glaxosmithkline is recalling ChapStick Total Hydration Moisture Tint Pretty in Pink due to observed separation in the secondary packaging.
Product
CHAPSTICK TOTAL HYDRATION MOISTURE TINT PRETTY IN PINK — CHAPSTICK TOTAL HYDRATION MOISTURE TINT PRETTY IN PINK (ZINC OXIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1266-2020·2020-05-20
ChapStick Lip Balm Recalled for Packaging Separation
Glaxosmithkline is recalling 288 packages of ChapStick Total Hydration Moisture Tint Peachy Keen due to observed separation in the secondary packaging.
Product
CHAPSTICK TOTAL HYDRATION MOISTURE TINT PEACHY KEEN — CHAPSTICK TOTAL HYDRATION MOISTURE TINT PEACHY KEEN (ZINC OXIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V282000·2020-05-19
Altec Recalls Aerial Devices and Digger Derricks Due to Bolt Failure Risk
Altec is recalling 2018-2020 aerial devices and digger derricks because bolts securing the pedestal to the turntable may fail, increasing the risk of injury or death.
Product
ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V279000·2020-05-18
Mitsubishi Recalls Lancer and Outlander Models for Corroded Front Cross Members
Mitsubishi is recalling specific Lancer, Outlander, and Outlander Sport vehicles because front cross members may corrode and detach, increasing crash risk.
Product
MITSUBISHI — MITSUBISHI LANCER, OUTLANDER, OUTLANDER SPORT, LANCER SPORTBACK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V281000·2020-05-18
Western Star 4700 and 5700 trucks recalled for ground harness wiring defect
DTNA is recalling certain 2019-2021 Western Star 4700 and 5700 trucks. An undersized wire in the ground harness may cause a melted connector, leading to engine stall and increasing crash risk.
Product
WESTERN STAR — WESTERN STAR 4700, 5700
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V280000·2020-05-18
Mitsubishi Recalls Outlander Models Due to Second-Row Seat Belt Assembly Defect
Mitsubishi is recalling 2019-2020 Outlander and 2019 Outlander PHEV vehicles because the right-side second-row seat belt may be assembled incorrectly, potentially failing to restrain occupants in a crash.
Product
MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER PHEV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V276000·2020-05-15
Forest River Recalls 2019-2020 XLR Micro Boost Trailers for Ramp Door Fastener Issue
Forest River is recalling 2019-2020 XLR Micro Boost trailers because ramp door fasteners may loosen, causing the door to detach and potentially leading to injury or a crash.
Product
FOREST RIVER — FOREST RIVER XLR MICRO BOOST
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V278000·2020-05-15
Vantage Recalls Modified Dodge Grand Caravans Due to Fuel Pump Gasket Leak
Vantage Mobility International is recalling 2016-2019 modified Dodge Grand Caravans because a deteriorating fuel pump gasket may cause fuel leaks, increasing fire risk.
Product
DODGE — DODGE GRAND CARAVAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V277000·2020-05-15
Yamaha Recalls 2015-2018 XC155 Scooters Due to Cylinder Head Nut Issue
Yamaha is recalling 2015-2018 XC155 scooters because cylinder head nuts may loosen, causing coolant to foul the spark plug and potentially leading to engine stalling.
Product
YAMAHA — YAMAHA SMAX, XC155F
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·20122·2020-05-14
Garia Recalls Electric Golf and Courtesy Vehicles Due to Fire Hazard
Garia is recalling about 1,000 battery-powered golf and courtesy vehicles because a fuse can overheat and melt while charging, posing a fire hazard.
Product
Garia Golf & Courtesy battery-powered electric vehicles
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·20744·2020-05-14
John Deere Recalls Broom Attachment Kits Due to Missing Manual
John Deere is recalling 60-inch broom attachment kits for compact utility tractors because they lack the required Operator's Manual, posing an injury hazard.
Product
Attachment Kits for John Deere 60-inch Brooms
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20742·2020-05-14
Aromatics International Recalls Wintergreen Essential Oil for Packaging Defect
Aromatics International is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
Product
Aromatics International Wintergreen Essential Oil
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20743·2020-05-14
Jade Bloom Essential Oils Recalled for Non-Child-Resistant Packaging
W8 Distributing is recalling Jade Bloom Wintergreen and Birch Sweet Essential Oils because the packaging is not child-resistant, posing a poisoning risk to young children.
Product
Jade Bloom Wintergreen and Birch Sweet Essential Oils
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20121·2020-05-14
Flybar Recalls Swurfer Kiwi Baby and Toddler Swings Due to Fall Hazard
Flybar is recalling Swurfer Kiwi Baby and Toddler Swings because a plastic stopper can detach, posing a fall hazard to the occupant.
Product
Swurfer Kiwi Baby and Toddler Swings
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·20V275000·2020-05-14
Heartland Recalls 2020 Trailers Due to Spare Tire Carrier Defect
Heartland is recalling 2020 Trail Runner, Wilderness, Mallard, and Prowler trailers because a U-bolt on the spare tire carrier may break, causing the tire to detach.
Product
HEARTLAND — HEARTLAND MALLARD, TRAIL RUNNER, WILDERNESS, PROWLER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·20745·2020-05-14
Organic Pure Oil Recalls Wintergreen Essential Oil for Packaging Defect
Organic Pure Oil is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
Product
Organic Pure Oil Wintergreen Essential Oil
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20123·2020-05-14
Sterno Home Recalls Path Light Kits Due to Electric Shock Hazard
Sterno Home is recalling Hampton Bay, Patriot, and Paradise path light kits because a defective power supply poses an electric shock risk.
Product
Hampton Bay, Patriot Lighting and Paradise light kits with Sterno Home LED power supplies
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1847-2020·2020-05-13
Applied Medical Recalls Bard Embolectomy Catheters Due to Tip Separation
Applied Medical Resources Corp is recalling Bard Embolectomy Catheters because the tips may separate during use, posing a risk of dislodgement in patients.
Product
Bard Embolectomy Catheter & 1 ml SYRINGE, REF numbers/UDI: CE0340DR/(01)H699CE0340DR10R; CE0380DR/(01)H699CE0380DR10V; CE0440DR/(01)H699CE0440DR10S; CE0480DR/(01)H699CE0480DR10W; CE0540DR/(01)H699CE0540DR10T; CE0580DR/(01)H699CE0580DR10X…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1846-2020·2020-05-13
Applied Medical Recalls Python Embolectomy Catheters Due to Tip Separation
Applied Medical Resources Corp is recalling Python Embolectomy Catheters because the tips may separate during use, posing a risk of unintended dislodgement in patients.
Product
Python Embolectomy Catheters, Sterile EO, CE, Ref numbers/UDI: A4E01/(01)00607915113407; A4E02/(01)00607915113414; A4E03/(01)00607915113421; A4E04/(01)00607915113438; A4E05/(01)00607915113445; A4E06/(01)00607915113452; A4E08/(01)00607915113476; A4E09/(01)00607915113483
Category
Medical Device
Distribution
Distributed nationwide