State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41926–41950 of 73919

ModerateFDA (Devices)·Z-2765-2017·2017-08-02
Medtronic DLP Antegrade/Retrograde Adapter Recalled for Packaging Pinholes
Medtronic is recalling DLP Antegrade/Retrograde Adapters because small pinholes were found in a single packaging configuration of sterile pouches.
Product
DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia alternately in either an antegrade or retrograde fashion. It is fitted with flexible lines and standard luer sites to facilitate direct connections to the cannulae
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2768-2017·2017-08-02
Medtronic Recalls DLP Pressure Display Sets Due to Packaging Pinholes
Medtronic Perfusion Systems is recalling DLP Pressure Disposable Pressure Display Sets because small pinholes were found in the sterile packaging.
Product
DLP Pressure Disposable Pressure Display Sets Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2761-2017·2017-08-02
Atrium iCAST and Advanta V12 Stents Recalled for Incorrect Hub Labeling
Atrium Medical Corporation is recalling specific iCAST and Advanta V12 covered stents because the catheter hub was printed with incorrect dimensional information.
Product
Atrium iCAST Balloon Expandable Covered Stent; 7mm x 22mm x 120cm; Model/Part Number 85455 (Marketed in U.S. only) Atrium Advanta V12 Balloon Expandable Covered Stent; 7mm x 22mm x 120cm; Model/Part Number 85355 (Marketed OUTSIDE U.S. only) The iCAST Covered Stent is…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2766-2017·2017-08-02
Medtronic Recalls DLP Cardioplegia Adapters Due to Packaging Pinholes
Medtronic Perfusion Systems is recalling DLP Cardioplegia Adapters with Pressure Port because small pinholes were identified in a single packaging configuration of sterile pouches.
Product
DLP Cardioplegia Adapter with Pressure Port Provides access for a pressure monitoring needle near the connection to the cardioplegia cannula. These adapters are intended for use in conjunction with the delivery of cardioplegia solution and to provide access for pressure…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2757-2017·2017-08-02
Cardinal Health Recalls Mislabeled Sterile Surgical Drapes
Cardinal Health is recalling specific lots of sterile surgical drapes because the outer labels do not match the packaged product inside.
Product
Converters(R) Under Buttocks Drape with Fluid Control Pouch II, REF 8482, STERILE R, Qty. 1, Cardinal Health, Waukegan, IL A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2758-2017·2017-08-02
Cardinal Health Recalls Tiburon Arthroscopy Drapes Due to Labeling Mismatch
Cardinal Health is recalling specific lots of Tiburon Arthroscopy Drapes because the outer labels do not match the packaged product.
Product
Converters(R) Tiburon(R) Arthroscopy Drape, REF 9414, STERILE EO, Qty. 1, Cardinal Health, Waukegan, IL A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as to isolate a site of…
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·17196·2017-08-01
MixBin Recalls Liquid Glitter iPhone Cases Due to Skin Irritation Risk
MixBin Electronics is recalling liquid glitter iPhone cases because the contents can leak and cause skin irritation or chemical burns.
Product
Liquid glitter iPhone cases
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17E042000·2017-08-01
Timken Recalls Rear Hub Unit Bearings for Ford Explorers
Timken is recalling specific rear hub unit bearings for 2011-2017 Ford Explorer 4X2 vehicles because they lack a self-retention feature, which could cause the wheel to separate.
Product
SUSPENSION:REAR recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V483000·2017-08-01
Utility VS2RA Trailer Recall for Detaching Mud Flap Bracket
Utility Trailer is recalling 2017 VS2RA trailers because a weld defect may allow the mud flap bracket to detach, creating a road hazard.
Product
UTILITY — UTILITY VS2RA
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17192·2017-08-01
Panelcraft Recalls Children's Magnetic Building Sets Due to Choking Hazard
Panelcraft is recalling Rainbow Dream Builder and Solid Builder sets because corner welds can break, releasing magnets that pose a choking hazard to children.
Product
Children's magnetic building sets
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17E040000·2017-07-28
Carli Suspension Recalls Adjustable Track Bars for Ram Trucks
Carli Suspension is recalling adjustable track bars for specific Ram trucks because a joint may break, causing loss of steering and increasing crash risk.
Product
SUSPENSION recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V482000·2017-07-28
Chrysler Pacifica Recall: Rear Pinion Bracket Cracking Risk
Vantage Mobility International is recalling 2017 Chrysler Pacifica lowered floor vehicles because rear pinion brackets may crack, causing wheel wobble and potential loss of control.
Product
CHRYSLER — CHRYSLER PACIFICA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V479000·2017-07-28
Daimler Recalls 2010-2011 Sprinter Vehicles for Air Bag Inflator Rupture Risk
Daimler Vans USA is recalling 2010-2011 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because passenger air bag inflators may rupture during deployment.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17E041000·2017-07-28
Dana Spicer Steer Axles Recalled for Potential Steering Loss
Dana is recalling Spicer D-Series and E-Series steer axles because the castellated nut may not be properly torqued, allowing the tie rod to loosen and potentially disconnect.
Product
STEERING:LINKAGES:TIE ROD ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V480000·2017-07-28
Daimler Recalls 2012 Freightliner and Mercedes-Benz Sprinter Vehicles for Air Bag Defect
Daimler Vans USA is recalling 2012 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because the passenger air bag inflators may rupture during deployment, posing a risk of serious injury or death.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·17760·2017-07-28
Nestlé Waters Recalls AccuPure Dispensers Due to Fire and Burn Hazards
Nestlé Waters is recalling about 12,300 AccuPure floor-standing filtration dispensers because they can overheat, smoke, or catch fire. No injuries have been reported.
Product
AccuPure floor-standing filtration dispensers
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17V478000·2017-07-28
Daimler Recalls 2007-2009 Sprinter Vehicles for Air Bag Inflator Defect
Daimler Vans USA is recalling 2007-2009 Dodge and Freightliner Sprinter 2500 and 3500 vehicles because passenger air bag inflators may rupture in a crash.
Product
DODGE — DODGE, FREIGHTLINER SPRINTER 2500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V481000·2017-07-28
BMW Recalls Motorcycles with Blocked Rear Reflex Reflectors
BMW is recalling specific motorcycles because optional aluminum luggage cases may block rear reflex reflectors, increasing crash risk.
Product
BMW — BMW F800 GS, F650 GS, F800 GS ADVENTURE, F800 R
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V476000·2017-07-27
Nissan Recalls Infiniti Q50 and Q60 for Fuel Pump Software Defect
Nissan is recalling 2016-2018 Infiniti Q50 and 2017 Q60 vehicles with 2.0L engines because faulty fuel pump software may cause the engine to stall while driving.
Product
INFINITI — INFINITI Q50, Q60
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17757·2017-07-27
Really Good Stuff Recalls Magnetic Dry Erase Boards Due to Laceration Hazard
Really Good Stuff is recalling Write Again magnetic dry erase boards because the metal surface can separate, posing a laceration hazard.
Product
Write Again® magnetic dry erase white boards
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·17V477000·2017-07-27
REV Recalls 2017-2018 Motorhomes With Non-Tempered Headlight Lenses
REV Recreation Group is recalling 219 motorhomes because headlights may lack tempered glass lenses, which could crack and reduce visibility.
Product
HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD, MONACO VACATIONER XE, ADMIRAL XE, STORM, FLAIR
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2740-2017·2017-07-26
Flowonix Recalls Prometra II Pump After Reported Fatal Overdose During MRI
Flowonix Medical is recalling Prometra II implantable infusion pumps after a report of a fatal drug overdose during an MRI procedure.
Product
PROMETRA II Programmable Infusion Pump, Implantable Infusion Pump, Catalog Number/REF 13827, Part Number PL-31790-02. Manufactured by: Flowonix Medical Inc., --- The correction involves the labeling of the device plus the following Prometra II pump labeling is also being…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2702-2017·2017-07-26
Penumbra 3D Revascularization Device Recalled Due to Delivery Wire Breakage Risk
Penumbra Inc. is recalling 155 units of the 3D Revascularization Device because a raw material issue could cause the delivery wire to break, potentially leading to serious injury or death.
Product
Penumbra 3D Revascularization Device It is indicated for used in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral-M1 and M2 segments) within 8 hours of symptom…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2819-2017·2017-07-26
Aldi Millville Granola Recalled for Listeria Contamination Risk
New England Natural Bakers is recalling Aldi Millville Fruit & Nut Whole Grain Granola due to potential Listeria monocytogenes contamination.
Product
Millville Fruit & Nut Whole Grain Granola - 16 oz .carton Distributed by Aldi Inc. Batavia, IL 60510 UPC:041498205232
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2817-2017·2017-07-26
Evoke Organic Muesli Recalled Due to Listeria Contamination Risk
New England Natural Bakers is recalling Evoke Organic Muesli Classic Swiss 12 oz. pouches due to potential Listeria monocytogenes contamination.
Product
Evoke Organic Muesli Classic Swiss 12 oz. pouch UPC: 853305003081
Category
Food
Distribution
Distributed nationwide