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.

60301–60325 of 74011

ModerateFDA (Drugs)·D-327-2014·2013-12-18
Novartis Recalls Diovan and Other Tablets Due to Chemical Contamination
Novartis is recalling physician sample bottles of Diovan and other tablets because they were contaminated with Darocur 1173, a photocuring agent used in inks.
Product
Diovan (valsartan) 320 mg per tablet, 7 Tablets per bottle, Rx only Physician Sample Not For Sale, Manufactured by: Novartis Pharmaceuticals Corporation Suffern, NY 10901 for Novartis Pharmaceuticals Corporation East Hanover, NJ 07936, NDC # 0078-9360-07
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-328-2014·2013-12-18
Novartis Recalls Exforge Physician Samples Due to Chemical Contamination
Novartis is recalling Exforge physician sample bottles due to contamination with Darocur 1173, a photocuring agent found in ink.
Product
Exforge (amlodipine and valsartan Tablets) 5/160 mg, Rx only 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936 - NDC # 0078-9488-07
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0482-2014·2013-12-18
Accumetrics Recalls VerifyNow IIb/IIIa Test Kits Due to Incorrect Instructions
Accumetrics is recalling VerifyNow IIb/IIIa Test Kits because they contain incorrect instructions regarding the time limit for performing the test after sample collection.
Product
VerifyNow IIb/IIIa Test, 10-Test Kit, Catalog No. 85310, 10 tests/box; 690 total tests. The VerifyNow IIb/IlIa Test is a semi-quantitative, whole blood platelet function test used to measure glycoprotein (GP) lIb/IlIa receptor blockade in patients treated with abciximab or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0467-2014·2013-12-18
Stryker Recalls Accolade II Hip Stems Due to Packaging Error
Stryker is recalling 20 Accolade II Hip Stems because a Size #3 was found packaged with a Size #5. The error poses a risk of incorrect implant selection.
Product
1) Accolade II 127 Neck Angle Hip Stem, Size # 3 2) Accolade II 127 Neck Angle Hip Stem, Size #5 Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA Telephone # +1 201-831-5000 Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0471-2014·2013-12-18
Beckman Coulter Recalls LH 750 and LH 780 Hematology Systems
Beckman Coulter is recalling LH 750 and LH 780 Hematology Systems because optical degradation may delay reporting results for specific blood cell counts.
Product
Coulter LH 780 Hematology Analyzer, Part No. 723585, A90728 Product Usage: Coulter LH 780 Hematology Analyzer is a is a quantitative, automated hematology analyzer and leukocyte differential counter For In Vitro Diagnostic Use in clinical laboratories. The Coulter¿ LH 780…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0474-2014·2013-12-18
Synthes Trochanteric Fixation Nail Recalled for Incorrect Packaging Labeling
Synthes USA is recalling 12 Trochanteric Fixation Nails because the packaging incorrectly lists the nail's length and diameter.
Product
Synthes Trochanteric Fixation Nail As part of the Synthes Trochanteric Fixation Nail (TFN) System, the TFN Nail is intended to treat stable and unstable fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0475-2014·2013-12-18
Zimmer Trabecular Metal Total Ankle Talar Component Recall for Residue
Zimmer, Inc. is recalling specific Total Ankle Talar Components because routine monitoring found potential elevated levels of manufacturing residue on the implants.
Product
Zimmer Trabecular Metal Total Ankle Talar Component Left Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobility by restoring alignment, reducing pain and preserving the flexion/extension movement within the ankle joint.The Zimmer Trabecular…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-346-2014·2013-12-18
Lupin Recalls Ethambutol Hydrochloride Tablets Due to Impurity
Lupin Pharmaceuticals is recalling 4,896 bottles of Ethambutol Hydrochloride 400 mg tablets because of an out-of-specification impurity result.
Product
ETHAMBUTOL HYDROCHLORIDE — ETHAMBUTOL HYDROCHLORIDE (ETHAMBUTOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-338-2014·2013-12-18
Novartis Recalls Tekturna Tablets Due to Chemical Contamination
Novartis is recalling Tekturna physician sample bottles contaminated with Darocur 1173, a photocuring agent found in ink.
Product
Tekturna (aliskiren) Tablets 300 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only. Manufactured by: Novartis Pharma Produktions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9486-07
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-334-2014·2013-12-18
Novartis Recalls Exforge Physician Samples Due to Chemical Contamination
Novartis is recalling Exforge physician sample bottles due to contamination with Darocur 1173, a photocuring agent found in ink.
Product
Exforge (amlodipine and valsartan, Tablets) 10/320 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9491-07
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0473-2014·2013-12-18
Synthes TomoFix Osteotomy System Recalled for Surgical Technique Guide Labeling Error
Synthes USA HQ, Inc. is recalling the TomoFix Osteotomy System due to a labeling error in the Surgical Technique Guide that may cause surgical delays.
Product
Synthes TomoFix Plates The Synthes J5606-C TomoFix Osteotomy System is used for open and closed wedge osteotomies of the medial proximal tibia, lateral proximal tibia, medial and lateral distal femur, treatment of bone and joint deformities, fractures, and malalignment caused…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0483-2014·2013-12-18
Stryker Recalls Cancellous Bone Screws Due to Packaging Error
Stryker is recalling specific Cancellous Bone Screws because a 5.5 mm screw was found in packaging labeled for a 6.5 mm screw.
Product
Stryker Orthopaedics Cancellous Bone Screw Howmedica Osteonics Corp. Stryker France Both the 6.4 mm diameter, 25mm length, Cancellous Bone Screws (Cat no 2030-6525-1) and the 5.5mm diameter, 40 mm length Cancellous Bone Screws (Cat no 2029-5540-1) are cleared for use in…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-330-2014·2013-12-18
Novartis Recalls Physician Sample Blood Pressure Medications Due to Chemical Contamination
Novartis is recalling physician sample bottles of several blood pressure and cholesterol medications due to contamination with a photocuring agent used in packaging inks.
Product
Exforge HCT (amlodipine, valsartan, hydrochlorothiazide) 10/320/25 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-339-2014·2013-12-18
Novartis Recalls Tekturna HCT Physician Samples Due to Chemical Contamination
Novartis is recalling physician sample bottles of Tekturna HCT and other medications due to contamination with Darocur 1173, a photo-curing agent.
Product
Tekturna HCT (aliskiren and hydrochlorothiazide) Tablets 150/12.5 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only, Manufactured by: Novartis Pharma Productions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-333-2014·2013-12-18
Novartis Recalls Physician Sample Blood Pressure Medications Due to Chemical Contamination
Novartis is recalling physician sample bottles of several blood pressure medications due to contamination with a photocuring agent found in packaging inks.
Product
Exforge (amlodipine and valsartan Tablets) 10/160 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9489-07
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-347-2014·2013-12-18
Taro Recalls Subpotent Ciclopirox Shampoo 1% Prescription Bottles
Taro Pharmaceuticals is recalling 850 bottles of Ciclopirox Shampoo 1% because the product is subpotent. The recall is voluntary and nationwide.
Product
CICLOPIROX — CICLOPIROX (CICLOPIROX)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0481-2014·2013-12-18
Ultradent Recalls Avex CX2 Ceramic Orthodontic Brackets Due to Design Control Issues
Ultradent is recalling 217 units of Avex CX2 Ceramic Orthodontic Brackets because the design control process was not completed before distribution.
Product
Opal Orthodontics by Ultradent. Avex CX2 Ceramic Orthodontic Brackets Avex CX2 ceramic brackets are intended for use in orthodontic treatment.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-341-2014·2013-12-18
Sandoz Recalls Bumetanide Tablets Due to Moisture Content Failures
Sandoz Inc. is recalling Bumetanide Tablets USP 0.5 mg because stability testing showed moisture content out of specification.
Product
BUMETANIDE — BUMETANIDE (BUMETANIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·13V627000·2013-12-17
Freightliner Recalls 2013-2014 Cascadia Trucks Due to Wiring Defect
Daimler Trucks North America is recalling 2013-2014 Freightliner Cascadia trucks because reversed wiring may reduce traction and parking brake effectiveness.
Product
FREIGHTLINER — FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·14061·2013-12-17
HP Chromebook 11 Chargers Recalled for Fire and Burn Hazards
Google and HP are recalling HP Chromebook 11 chargers because they can overheat and melt, posing fire and burn risks.
Product
HP Chromebook 11 power supply/charger
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·13V626000·2013-12-17
CJay Trailers Recall Cargo Trailers Due to Door Lock Jamming Risk
CJay is recalling specific cargo trailers because a defect in the door lock may jam the deadbolt, potentially trapping occupants inside the trailer.
Product
CJAY — CJAY CJ714, CJ814, CJ716, CJ820
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·13V625000·2013-12-17
Monaco Recalls 2008-2013 RVs With Potential Door Lock Jamming Defect
Monaco RV is recalling 3,175 recreational vehicles because a door lock defect may jam the deadbolt, potentially trapping occupants inside.
Product
MCKENZIE — MCKENZIE, R-VISION, HOLIDAY RAMBLER ION, SILVER CREEK, TRAIL CRUISER CLASSIC, TRAIL LITE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·13V633000·2013-12-16
Thomas Built Saf-T-Liner C2 School Bus Recall for Transmission Software
Daimler Trucks North America is recalling 2011-2013 Thomas Built Saf-T-Liner C2 school buses because transmission software may cause unintended acceleration.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES, THOMAS BUILT SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·13V624000·2013-12-16
Hyundai Recalls 2014 Santa Fe Vehicles Due to Tire Sidewall Defect
Hyundai is recalling 2014 Santa Fe vehicles equipped with specific Continental tires that may have damaged sidewalls, increasing the risk of tread detachment or rapid air loss.
Product
HYUNDAI — HYUNDAI SANTA FE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·13V622000·2013-12-16
Honda Recalls 2014 Acura RLX for Rear Suspension Bolt Issues
Honda is recalling 7,387 2014 Acura RLX vehicles because rear suspension bolts may have loosened, potentially reducing steering ability and increasing crash risk.
Product
ACURA — ACURA RLX
Category
Vehicle
Distribution
Distributed nationwide