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.

57976–58000 of 74005

SevereFDA (Devices)·Z-1823-2014·2014-07-02
FDA Recalls HydroFinity Hydrophilic Guidewires Due to Jacket Damage
Nitinol Devices and Components is recalling HydroFinity Hydrophilic Guidewires because the outer polymer jacket may be damaged during use.
Product
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Straight Tip, 260 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA; Manufactured in Costa Rica The HydroFinity…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1815-2014·2014-07-02
Nitinol Devices Recalls HydroFinity Hydrophilic Guidewires Due to Jacket Damage
Nitinol Devices and Components, Inc. is recalling HydroFinity Hydrophilic Guidewires because the outer polymer jacket may be damaged during use.
Product
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Straight Tip, 150 CM Length Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1819-2014·2014-07-02
Nitinol HydroFinity Hydrophilic Guidewire Recalled for Polymer Jacket Damage
Nitinol Devices and Components, Inc. is recalling HydroFinity Hydrophilic guidewires because reports indicate the outer polymer jacket may be damaged during use.
Product
HydroFinity Hydrophilic guidewire;Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA Manufactured in Costa Rica. The HydroFinity…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·14V398000·2014-07-02
Fontaine Recalls 2015 Magnitude 100 Trailers Due to Weld Defects
Fontaine is recalling 2015 Magnitude 100 lowbed trailers because inadequate welds may cause structural components to separate, increasing crash risk.
Product
FONTAINE — FONTAINE MAGNITUDE 100
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1812-2014·2014-07-02
FDA Recalls HydroFinity Hydrophilic Guidewires Due to Polymer Jacket Damage
Nitinol Devices and Components is recalling HydroFinity Hydrophilic Guidewires because the outer polymer jacket may be damaged during use.
Product
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Angled Tip, 150 CM Length Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·14V407000·2014-07-02
GM Recalls 2007-2011 Silverado and Sierra Trucks for Fire Risk
General Motors is recalling 2007-2011 Chevrolet Silverado and GMC Sierra HD trucks equipped with auxiliary batteries due to a risk of electrical fire.
Product
GMC — GMC, CHEVROLET SIERRA 3500, SIERRA 2500, SILVERADO 2500, SILVERADO 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1818-2014·2014-07-02
Nitinol Recalls HydroFinity Hydrophilic Guidewires Due to Jacket Damage
Nitinol Devices and Components is recalling HydroFinity Hydrophilic Guidewires because reports indicate the outer polymer jacket can be damaged during use.
Product
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled Tip, 150 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA Manufactured in Costa Rica The HydroFinity…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1813-2014·2014-07-02
Nitinol HydroFinity Hydrophilic Guidewire Recalled for Outer Polymer Jacket Damage
Nitinol Devices and Components is recalling HydroFinity Hydrophilic Guidewires because the outer polymer jacket may be damaged during use.
Product
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Angled Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1408-2014·2014-07-02
Teva Recalls Dextroamphetamine Sulfate Tablets Due to Impurity Test Failures
Teva Pharmaceuticals is recalling 9,882 bottles of Dextroamphetamine Sulfate 10 mg tablets because stability testing revealed out-of-specification impurities.
Product
DEXTROAMPHETAMINE SULFATE — DEXTROAMPHETAMINE SULFATE (DEXTROAMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1821-2014·2014-07-02
Nitinol HydroFinity Hydrophilic Guidewire Recalled for Outer Polymer Jacket Damage
Nitinol Devices and Components, Inc. is recalling HydroFinity Hydrophilic guidewires because the outer polymer jacket may be damaged during use.
Product
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Straight Tip, 150 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1814-2014·2014-07-02
Nitinol HydroFinity Hydrophilic Guidewire Recalled for Outer Polymer Jacket Damage
Nitinol Devices and Components is recalling HydroFinity Hydrophilic guidewires because reports indicate the outer polymer jacket may be damaged during use.
Product
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Angled Tip, 260 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·14V402000·2014-07-02
Ford Recalls 2014 Fiesta Vehicles Due to Fuel Tank Leak Risk
Ford is recalling certain 2014 Fiesta vehicles because a manufacturing error may cause the fuel tank to leak, increasing the risk of fire.
Product
FORD — FORD FIESTA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V397000·2014-07-02
Autocar Recalls 2012-2015 Xpert Trucks Due to Bounce Hazard
Autocar is recalling 287 model year 2012-2015 Xpert trucks because a gap between the cab and body may cause unexpected bouncing at speeds above 25 mph, increasing crash risk.
Product
AUTOCAR — AUTOCAR XPERT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V403000·2014-07-02
Ford Recalls 2014 Escape Vehicles for Panorama Roof Glass Bonding Defect
Ford is recalling 2014 Escape vehicles because the panorama roof glass may not be properly bonded, which could cause the glass to separate and increase the risk of a crash or injury.
Product
FORD — FORD ESCAPE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14E034000·2014-07-02
LiquidSpring Recalls Aftermarket Suspensions for Ford and Chevrolet Chassis
LiquidSpring is recalling specific aftermarket suspension units for Ford and Chevrolet chassis because a mounting bracket may fail, allowing the fluid tank to separate and become a road hazard.
Product
SUSPENSION recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V393000·2014-07-02
Ford and Lincoln Recall Vehicles for Halfshaft Retention Defect
Ford is recalling 2012-2014 Edge, MKX, Taurus, MKS, Flex, and MKT vehicles because a halfshaft may disengage, causing loss of power or vehicle roll-away.
Product
LINCOLN — LINCOLN, FORD MKS, FLEX, EDGE, TAURUS
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1854-2014·2014-07-02
NxStage Dialysate Sacks Recalled for Excess Aluminum Levels
NxStage Medical is recalling dialysate sacks used with the PureFlow SL system because they contain aluminum levels exceeding internal specifications.
Product
NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-301 Lactate 45, Potassium 1, Sodium 140, Calcium 3, Magnesium 1, Chloride 100, Glucose (mg/dL) 100 Batch Size (liters) 60 The SAK is one of the disposables used with NxStage PureFlow SL…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1925-2014·2014-07-02
Biomet Recalls Discovery Elbow Prosthesis Due to Surface Finish Defect
Biomet, Inc. is recalling one unit of a Discovery Elbow prosthesis because the surface finish differs from specifications, potentially causing pain requiring surgery.
Product
DISCOVERY ELBOW prosthesis, 4 MM X 100 MM RIGHT HUMERAL FLANGED I BOND COAT Tl 6AL 4V ALLOY. Elbow joint replacement prostheses are intended for primary and revision joint arthroplasty for use in cemented applications.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·14V409000·2014-07-02
GM Recalls 2014 Vehicles for Steering Component Separation Risk
General Motors is recalling 2014 Buick Regal, Cadillac XTS, Chevrolet Camaro, and Chevrolet Impala vehicles because improperly torqued fasteners may cause steering components to separate, increasing crash risk.
Product
CHEVROLET — CHEVROLET, BUICK, CADILLAC IMPALA, CAMARO, REGAL, XTS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V401000·2014-07-02
Ford Recalls F-59 Commercial Chassis Vehicles for Fire Risk
Ford is recalling 2011-2014 F-59 commercial chassis vehicles because a short circuit in the electrical system may cause a fire.
Product
FORD — FORD F-59
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V392000·2014-07-02
Chrysler Recalls 2014-2015 Vehicles for Rear Shock Absorber Weld Defect
Chrysler is recalling 2014 Jeep Cherokee, Ram 1500, and 2015 Chrysler 200 vehicles because an insufficient weld may cause rear shocks to detach, potentially damaging tires or reducing braking.
Product
CHRYSLER — CHRYSLER, RAM, JEEP 200, 1500, CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V456000·2014-07-02
Sutphen Minitower Fire Truck Seat Belt Buckle Recall
Sutphen is recalling one 2013 Minitower fire truck because seat belt buckles may fail to release, potentially hindering emergency egress.
Product
SUTPHEN — SUTPHEN MINITOWER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1874-2014·2014-07-02
Zynex IF 8000 Interferential Electrical Stimulation Device Recalled for Overheating
Zynex Medical is recalling 1,461 IF 8000 devices because a malfunction can cause them to stop working or overheat, posing a burn risk.
Product
IF 8000; 1/F Interferential Electrical Stimulation Device; NMES (neuromuscular electrical stimulation) mode. Designed for use in physical therapy, rehabilitation, and pain relief applications.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1859-2014·2014-07-02
NxStage Dialysate Sacks Recalled for Excess Aluminum Levels
NxStage Medical is recalling 2,711 cases of dialysate sacks because aluminum levels exceeded internal specifications.
Product
NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-306 Lactate 45, Potassium 2, Sodium 140, Calcium 3, Magnesium 1, Chloride 101, Glucose (mg/dL) 100 Batch Size (liters) 50 The SAK is one of the disposables used with NxStage PureFlow SL…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1409-2014·2014-07-02
Pfizer Recalls Pristiq 50 mg Tablets Due to Foreign 100 mg Tablet
Pfizer is recalling Pristiq 50 mg extended-release tablets because a 100 mg tablet was found in a bottle labeled for 50 mg.
Product
PRISTIQ — PRISTIQ (DESVENLAFAXINE SUCCINATE)
Category
Drug
Distribution
Distributed nationwide