State

US Virgin Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48126–48150 of 73987

ModerateFDA (Devices)·Z-2021-2016·2016-06-29
Siemens Biograph PET/CT Scanners Recalled for Calibration Error Risk
Siemens is recalling 28 Biograph mCT Flow 20-4R PET/CT scanners because using non-Siemens phantoms for calibration may result in unexpected SUV values.
Product
BIOGRAPH mCT Flow 20-4R, MATERIAL NUMBER 10528958 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2008-2016·2016-06-29
Siemens Biograph 40 TruePoint PET/CT Scanner Recall for Calibration Error
Siemens is recalling 48 Biograph 40 TruePoint PET/CT scanners because using non-Siemens phantoms for calibration may result in unexpected SUV values.
Product
BIOGRAPH 40 TruePoint, Material Number 10097303 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2007-2016·2016-06-29
Siemens Biograph 40 PET/CT Scanners Recalled for Calibration Error Risk
Siemens is recalling five Biograph 40 PET/CT scanners due to a potential for unexpected Standardized Uptake Value (SUV) readings when non-Siemens phantoms are used for calibration.
Product
BIOGRAPH 40 - 3 Ring, Material Number 10097233 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1039-2016·2016-06-29
Profarma Recalls tabcin ACTIVE M.R. Capsules Due to Manufacturing Deviations
Profarma Distributors LLC is voluntarily recalling 42 boxes of tabcin ACTIVE M.R. Capsules nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Product
tabcin ACTIVE M.R. Capsules, 12-count box , UPC 7501008485057
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1043-2016·2016-06-29
Profarma Recalls 1% Clotrimazole Cream Due to Manufacturing Deviations
Profarma Distributors LLC is recalling 79 tubes of 1% Clotrimazole cream due to CGMP deviations. The recall is voluntary and nationwide.
Product
1% Clotrimazol cream, 30 mg tube, UPC 501318644335
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2048-2016·2016-06-29
Medtronic Recalls Two EverFiex Stents Due to Outer Box Mislabeling
Medtronic is recalling two Protege EverFiex Self-expanding Peripheral Stent Systems from lot A164580 because the outer box size label may not match the device inside.
Product
EV3 EverFiex" Self-expanding Peripheral Stent System, Sterilized using Ethylene Oxide, Rx Only, PRB35-08-040-080. The Protege EverFiex" Self-expanding Peripheral Stent System is a self-expanding Nitinol stent system intended for permanent implantation. The self-expanding stent…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2025-2016·2016-06-29
Siemens Biograph PET/CT Scanners Recalled for Calibration Error Risk
Siemens is recalling 25 Biograph mCT Flow 64-4R scanners because using non-Siemens phantoms for calibration may result in unexpected SUV values.
Product
BIOGRAPH mCT Flow 64-4R, MATERIAL NUMBER 10529161 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2022-2016·2016-06-29
Siemens Biograph TruePoint PET/CT Scanners Recalled for Calibration Error
Siemens is recalling three Biograph TruePoint PET/CT scanners because using non-Siemens phantoms for calibration may result in unexpected SUV values.
Product
BIOGRAPH mCT Flow 40-3R, MATERIAL NUMBER 10529158 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2014-2016·2016-06-29
Siemens Biograph TruePoint PET/CT Scanners Recalled for Calibration Error
Siemens is recalling 16 Biograph TruePoint PET/CT scanners because using non-Siemens phantoms for calibration may result in unexpected SUV values.
Product
BIOGRAPH 64-3R TruePoint, MATERIAL NUMBER 10097301 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2027-2016·2016-06-29
Siemens Biograph PET/CT Scanners Recalled for Calibration Error Risk
Siemens is recalling 13 Biograph mCT Flow Edge-4R scanners because using non-Siemens phantoms for calibration may result in unexpected SUV values.
Product
BIOGRAPH mCT Flow Edge-4R, MATERIAL NUMBER 10528955 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1044-2016·2016-06-29
Virtus Recalls Hyoscyamine Sulfate Tablets Due to Broken Dessicants
Virtus Pharmaceuticals is recalling Hyoscyamine Sulfate Sublingual Tablets because bottles may contain broken dessicants.
Product
Hyoscyamine Sulfate Sublingual Tablets, 0.125 mg, packaged in 100-count bottles, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC. Nashville, TN 37217. NDC 76439-0309-10
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1048-2016·2016-06-29
Virtus Pharmaceuticals Recalls Leaking Prenatal/Postnatal Capsules
Virtus Pharmaceuticals is recalling 1,586 bottles of VP-CH-PNV Prenatal/Postnatal capsules because the softgel capsules are leaking.
Product
VP-CH-PNV Prenatal/Postnatal capsules, prenatal supplement, 30-count bottle, Rx only, Manufactured for: Virtus Pharmaceuticals, LLC, Tampa, FL 33619, NDC 69543-224-30
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1045-2016·2016-06-29
Sandoz Recalls Dicloxacillin Sodium Capsules Due to Impurity Testing Failures
Sandoz, Inc. is recalling Dicloxacillin Sodium Capsules because testing revealed out-of-specification results for a known impurity.
Product
Dicloxacillin Sodium Capsules, USP 250mg, Rx Only, 100 Capsule Bottle, Manufactured in Austria by Sandoz Gmbh, Distributed by Sandoz Inc., Princeton, NJ 08540, Product of Spain, NDC 0781-2248-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1049-2016·2016-06-29
Prinston Recalls Irbesartan and Hydrochlorothiazide Tablets Due to Labeling Error
Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because an incorrect lot number appears on the case label.
Product
IRBESARTAN AND HYDROCHLOROTHIAZIDE — IRBESARTAN AND HYDROCHLOROTHIAZIDE (IRBESARTAN AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2039-2016·2016-06-29
Leica Biosystems Recalls CytoVision Systems Due to Windows 7 Activation Issues
Leica Biosystems Richmond Inc. is recalling 283 CytoVision Image Analysis and Capture Systems because the Windows 7 operating system is improperly activated, appearing unlicensed.
Product
CytoVision Image Analysis and Capture System, an automated cell-locating device. The Cytovision is a rapid metaphase finder, image acquisition and computer aided chromosome analysis system which assists the operator in viewing chromosomes and looking for cellular anomalies.…
Category
Medical Device
Distribution
Distributed nationwide
CriticalCPSC·16204·2016-06-28
IKEA Recalls 29 Million Chests and Dressers Due to Tip-Over Hazard
IKEA is recalling 29 million chests and dressers in the U.S. due to a serious tip-over hazard that has caused three child deaths and 17 injuries.
Product
Children's and adult chests and dressers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·16755·2016-06-28
Polaris Recalls Ranger 570 ROVs Due to Fire Hazard
Polaris is recalling approximately 43,000 Ranger 570 recreational off-road vehicles because they can overheat and catch fire. Consumers should stop using these vehicles and contact Polaris for a free repair.
Product
Polaris Ranger 570 ROVs
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·16V473000·2016-06-28
Strick Recalls 2015 and 2017 Tandem Axle Van Trailers for Brake Defect
Strick Trailers is recalling specific 2015 and 2017 tandem axle van trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Product
STRICK — STRICK TANDEM AXLE VAN TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V476000·2016-06-28
Great Dane Trailers Recall 2015-2017 Models Due to Brake Valve Defect
Great Dane is recalling 2015-2017 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Product
GREAT DANE — GREAT DANE DRY FREIGHT VAN, REFRIGERATED TRAILER, FLATBED TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V479000·2016-06-28
Ford Recalls 2015-2016 Focus Electric Vehicles for Transmission Defect
Ford is recalling 865 model year 2015-2016 Focus Electric vehicles because the transmission's differential pinion gear shaft may overheat and fracture, potentially causing a loss of motive power and park function.
Product
FORD — FORD FOCUS ELECTRIC
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V474000·2016-06-28
Cheetah Chassis Recalls Trailers Due to Spring Brake Valve Defect
Cheetah Chassis is recalling specific 2014-2016 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Product
CHEETAH — CHEETAH FLATBED TRAILER, EXTENDABLE CHASSIS, BRIDGEMASTER CHASSIS, CURTAINSIDE FLATBED
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V472000·2016-06-28
Forest River Charleston Motorhomes Recalled for Throttle Sensor Defect
Forest River is recalling 2014-2016 Charleston motorhomes because a throttle sensor defect may prevent the engine brake from activating, increasing crash risk.
Product
FOREST RIVER — FOREST RIVER CHARLESTON
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V475000·2016-06-28
Ford Recalls 2016 Explorer and F-150 for Seat Back Weld Defect
Ford is recalling 2016 Explorer and F-150 vehicles with manual recline driver's seats because insufficient welds may compromise occupant restraint during a crash.
Product
FORD — FORD EXPLORER, F-150
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V477000·2016-06-28
Terex Recalls 2015-2016 Aerial Devices Due to Platform Tilt Risk
Terex is recalling 2015-2016 HR, HRX, TC, and TCX aerial devices because poor welds on the platform leveling cylinder may cause the platform to tilt, risking occupant falls.
Product
TEREX — TEREX HRX, HR, TC, TCX
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V478000·2016-06-28
Newmar Recalls 2014-2016 Motorhomes Due to Throttle Pedal Sensor Defect
Newmar is recalling 1,243 motorhomes because a throttle pedal sensor may fail, preventing the engine brake from activating and reducing braking ability.
Product
NEWMAR — NEWMAR DUTCH STAR, MOUNTAIN AIRE, LONDON AIRE, ESSEX
Category
Vehicle
Distribution
Distributed nationwide