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.

58951–58975 of 74011

ModerateFDA (Drugs)·D-1181-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Ear Drops
Hill Dermaceuticals is recalling 13,591 bottles of Fluocinolone Acetonide 0.01% Oil Ear Drops because routine testing found the active ingredient to be subpotent.
Product
SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Oil EAR DROPS, 20 ml, Rx only Manufactured by: Hill Dermaceuticals, Inc. For: Seton Pharmaceuticals NDC 13925-508-20
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1300-2014·2014-04-02
Bard Access Systems Recalls PowerPort Slim Implantable Ports Due to Labeling Error
Bard Access Systems is recalling 777 PowerPort Slim Implantable Ports because the labels incorrectly state they contain silicone suture plugs, when some units do not.
Product
PowerPort Slim Implantable Port, indicated for patient therapies requiring repeated access to the vascular system. Product Codes: 1716000, 1716070
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1273-2014·2014-04-02
Spacelabs Recalls G2 Clinical Access Software CDs Due to Incorrect Programs
Spacelabs Healthcare is voluntarily recalling G2 Clinical Access Software CDs because they contain incorrect programs, preventing customers from installing the software.
Product
Spacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11 Rev A and Update Kit, PN: 040-1565-10. Used for installing ICS G2 Clinical Access software onto hospital personal computers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1268-2014·2014-04-02
AMS Uric Acid Test Kits Recalled for Regulatory Violations
AMS Diagnostics is recalling 13 Uric Acid test kits because they were marketed outside FDA 510(k) requirements.
Product
AMS URIC ACID For the In vitro quantitative determination of Uric Acid in serum Quantitative determination of Uric Acid in serum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1269-2014·2014-04-02
AMS AST Diagnostic Kits Recalled for Marketing Outside 510(k) Requirements
AMS Diagnostics is recalling 116 AMS AST kits because they were marketed outside FDA 510(k) requirements. The recall covers nationwide distribution.
Product
AMS AST For the In vitro quantitative determination of AST in serum Quantitative determination of AST in serum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1178-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Dermotic Ear Drops
Hill Dermaceuticals is recalling Dermotic ear drops because the active ingredient was found to be subpotent during routine testing.
Product
DERMOTIC — DERMOTIC (FLUOCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1180-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil
Hill Dermaceuticals is recalling 7,676 bottles of Fluocinolone Acetonide 0.01% Topical Oil because the active ingredient was found to be subpotent during routine testing.
Product
SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Topical Oil (Body Oil), 4 fl.oz., Rx only Manufactured by: Hill Dermaceuticals, Inc. For: Seton Pharmaceuticals NDC 13925-506-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1176-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil
Hill Dermaceuticals is recalling 8,734 bottles of Derma-Smoothe/FS topical oil because the active ingredient was found to be subpotent during routine testing.
Product
DERMA-SMOOTHE/FS — DERMA-SMOOTHE/FS (FLUOCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1267-2014·2014-04-02
AMS BUN Urea Nitrogen Kits Recalled for Marketing Violations
AMS Diagnostics is recalling 167 BUN Urea Nitrogen kits because they were marketed outside FDA 510(k) requirements.
Product
AMS BUN UREA NITROGEN For the In vitro quantitative determination of Urea Nitrogen in serum Quantitative determination of Bun in serum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1175-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil
Hill Dermaceuticals is recalling 8,734 bottles of Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil because the active ingredient was found to be subpotent during routine testing.
Product
Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Body Oil) 4 fl. oz., Rx only Manufactured and Distributed by: Hill Dermaceuticals, Inc. Sanford, Florida 32773 NDC 28105-150-04
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1173-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent DermOtic Oil Ear Drops
Hill Dermaceuticals is recalling DermOtic Oil ear drops because the active ingredient was found to be subpotent during routine testing.
Product
DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops, 20 mL bottle, Rx only Manufactured and Distributed by: Hill Dermaceuticals, Inc. Sanford, Florida 32773 NDC 28105-160-20
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1174-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil
Hill Dermaceuticals is recalling 14,226 bottles of Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil because the active ingredient was found to be subpotent during routine testing.
Product
Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Scalp Oil), 4 fl. oz., Rx only. Manufactured and Distributed by: Hill Dermaceuticals, Inc. Sanford, Florida 32773 NDC 28105-149-04
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1177-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Scalp Oil
Hill Dermaceuticals is recalling 7,292 bottles of Derma-Smoothe/FS scalp oil because the active ingredient was found to be subpotent during routine testing.
Product
DERMA-SMOOTHE/FS — DERMA-SMOOTHE/FS (FLUOCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·14V161000·2014-04-01
Chrysler Recalls 2014 Ram 1500 4x4 Trucks for Transmission Defect
Chrysler is recalling 125 model year 2014 Ram 1500 4x4 vehicles because the transmission case may be improperly machined, preventing the park pawl from engaging and increasing the risk of a crash.
Product
RAM — RAM 1500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14E012000·2014-04-01
Ohlins Recalls Steering Damper Kits for Cracking Bracket Risk
Ohlins Racing AB is recalling steering damper kits for various motorcycles because an incorrectly machined bracket may crack, potentially causing steering to lock at low speeds.
Product
DUCATI — DUCATI, SUZUKI, YAMAHA 996, 998, GSX1300R, 848
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V154000·2014-04-01
Chrysler Recalls 2011-2014 Jeep Grand Cherokee and Dodge Durango for Brake Booster Defect
Chrysler is recalling 2011-2014 Jeep Grand Cherokee and Dodge Durango vehicles because a corroding brake booster may allow water to enter, potentially freezing and limiting braking ability.
Product
JEEP — JEEP, DODGE GRAND CHEROKEE, DURANGO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14C002000·2014-04-01
Baby Trend Recalls 2011-2012 TrendZ Fastback Child Restraints for Buckle Defect
Baby Trend is recalling 2011 and 2012 TrendZ Fastback 3-in-1 child restraints because the harness buckle may become stuck, making it difficult to remove a child in an emergency.
Product
CHILD SEAT:HARNESS/CROTCH BUCKLE recall
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·14143·2014-04-01
Dyson Recalls Bladeless Portable Electric Heaters Due to Fire Hazard
Dyson is recalling about 338,000 portable electric heaters in the U.S. because they can short-circuit and overheat, posing a fire hazard.
Product
Portable electric heaters
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·14V152000·2014-03-31
GM Recalls 2014-2015 Trucks and SUVs for Transmission Oil Fire Risk
General Motors is recalling specific 2014-2015 Chevrolet and GMC vehicles because a transmission oil cooler line may not be securely seated, creating a potential fire hazard.
Product
CHEVROLET — CHEVROLET, GMC SILVERADO, YUKON, TAHOE, SUBURBAN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V156000·2014-03-31
Crossroads Recalls 2015 Trailers Due to Brittle Spring Hangers
Crossroads RV is recalling 2015 Zinger, Rezerve, and Sunset Trail trailers because brittle frame spring hangers may fracture, increasing crash risk.
Product
CROSSROADS — CROSSROADS SUNSET TRAIL, ZINGER, REZERVE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V181000·2014-03-31
Jaguar Recalls 2013-2014 XF Models Due to Loose Charge Air Cooler Hose Clamp
Jaguar is recalling 2013-2014 XF 2.0L GTDi vehicles because a loose hose clamp may allow the Charge Air Cooler hose to detach, potentially causing the engine to stall and loss of steering and brake assistance.
Product
JAGUAR — JAGUAR XF
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V157000·2014-03-31
Jaguar Recalls 2013-2014 XJ, XF, and XK for Rear Suspension Defect
Jaguar is recalling 2013-2014 XJ, XF, and XK vehicles because rear toe links can separate, potentially causing loss of vehicle control and increasing crash risk.
Product
JAGUAR — JAGUAR XF, XJ, XK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V151000·2014-03-31
GM Recalls 2013-2014 Chevrolet Cruze for Right Front Half Shaft Fracture Risk
General Motors is recalling 2013-2014 Chevrolet Cruze vehicles with 1.4L turbo engines because the right front half shaft may fracture, potentially causing loss of power or unexpected vehicle movement.
Product
CHEVROLET — CHEVROLET CRUZE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V155000·2014-03-31
Land Rover Recalls 2014 Range Rover Evoque for Rear Suspension Bolt Defect
Land Rover is recalling 2014 Range Rover Evoque vehicles because damaged rear suspension bolts may fail, causing the link arm to separate and increasing crash risk.
Product
LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14E011000·2014-03-31
Speedway Motors Recalls Brake Light Switches Due to Fluid Leak Risk
Speedway Motors is recalling specific brake light switches used in hot rods that may crack, causing brake fluid leaks and increased stopping distances.
Product
EXTERIOR LIGHTING:BRAKE LIGHTS:SWITCH recall
Category
Vehicle
Distribution
Distributed nationwide