State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53576–53600 of 74002

HighFDA (Devices)·Z-1752-2015·2015-06-17
Gyrus ACMI Diego Elite Tubeset Recalled for Sterility Assurance Concerns
Gyrus Acmi is recalling Diego Elite Tubesets due to a potential lack of sterility assurance. The recall affects 12,020 boxes distributed in the US, Canada, and other countries.
Product
Gyrus ACMI Diego Elite Tubeset; intended for cutting, coagulation, drilling, debriding, and removal of bone, and soft and hard tissue in general ENT, Sinus/Rhinology, Nasopharyngeal/Laryngology, and Head & Neck procedures. Catalog No. TS100S, Lot numbers JC929332 and below…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2396-2015·2015-06-17
Reaction Nutrition Recalls Amino Action Supplements Due to Undeclared Whey
Reaction Nutrition is recalling Amino Action supplements because they may contain undeclared whey protein due to shared equipment use.
Product
REACTION RECOR: Amino Action- 500g (Glacier Blue), Distributed by Reaction Nutrition, Carnegie, PA
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2400-2015·2015-06-17
Reaction Nutrition Recalls Pre-Workout Supplements for Potential Allergen Contamination
Reaction Nutrition is recalling REACTION RECOR: Pre Action supplements because they may contain undeclared whey protein and soy.
Product
REACTION RECOR: Pre Action- 336g Glacier Blue, Distributed by Reaction Nutrition, Carnegie, PA
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1792-2015·2015-06-17
Philips Recalls BrightView XCT UPS Accessory Devices for Battery Acid Leakage
Philips Medical Systems is recalling 337 BrightView XCT UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Product
BrightView XCT (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·15166·2015-06-17
Colnago Recalls CF10 and V1-r Bicycles Due to Brake Detachment Hazard
Colnago America is recalling CF10 and V1-r racing bicycles and frame kits because the front brakes can detach from the fork, posing a crash hazard.
Product
Bicycles and bicycle frame kits
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1772-2015·2015-06-17
Philips Medical Systems Recalls Ingenuity Core 128 UPS Accessory Devices
Philips Medical Systems is recalling 288 Ingenuity Core 128 UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Product
Ingenuity Core 128 (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1744-2015·2015-06-17
Biomet Optigun Ratchet Cement Gun Recalled Due to Pin Disconnection Risk
Biomet France is recalling three Optigun Ratchet cement guns because a pin may disconnect and be lost, potentially delaying surgery or requiring revision.
Product
The Optigun Ratchet is a hand-held cement gun for use with Optivac. The Optigun Ratchet is used to deliver bone cement from the Optivac.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1764-2015·2015-06-17
Philips Recalls CT Scanner UPS Accessories Due to Battery Acid Leakage Risk
Philips Medical Systems is recalling 126 UPS accessory devices for CT scanners due to risks of battery acid leakage, overheating, and fume emission.
Product
Brilliance CT Big Bore Radiology (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1775-2015·2015-06-17
Philips Medical Systems Recalls AXIS UPS Accessory Devices for CT Systems
Philips Medical Systems is recalling AXIS Uninterruptible Power Supply (UPS) accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Product
AXIS (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1777-2015·2015-06-17
Philips Medical Systems Recalls Forte-JetStream AZ UPS Accessory Devices
Philips Medical Systems is recalling 11 Forte-JetStream AZ UPS accessory devices used in CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fumes.
Product
Forte-JetStream AZ (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1790-2015·2015-06-17
Philips BrightView X UPS Accessory Devices Recalled for Battery Acid Leakage
Philips Medical Systems is recalling 108 BrightView X UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Product
BrightView X (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1771-2015·2015-06-17
Philips Medical Systems Recalls Ingenuity Core UPS Accessory Devices
Philips Medical Systems is recalling 215 Ingenuity Core UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Product
Ingenuity Core (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1714-2015·2015-06-17
ASP Recalls EVOTECH Endoscope Cleaner for Connection Detection Failure
Advanced Sterilization Products is recalling EVOTECH Endoscope Cleaner and Reprocessor units because they may fail to detect disconnected endoscopes, allowing the cleaning cycle to complete without proper processing.
Product
EVOTECH Endoscope Cleaner and Reprocessing System 208V, P/N 50004. The ASP EVOTECH ECR Endoscope Cleaner and Reprocessor is a washer/disinfector, which is indicated for use with high-level disinfectant CIDEX OPA Concentrate and an enzymatic detergent (CIDEZYME Gl) to achieve…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1763-2015·2015-06-17
Philips Brilliance CT 40 Uninterruptible Power Supply Recall
Philips is recalling Brilliance CT 40 Uninterruptible Power Supply accessories due to risks of battery acid leakage, overheating, and fume emission.
Product
Brilliance CT 40 - Slices(Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1788-2015·2015-06-17
Philips Recalls GEMINI TF Ready UPS Accessory Devices for CT Systems
Philips Medical Systems is recalling three GEMINI TF Ready UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fumes.
Product
GEMINI TF Ready (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1758-2015·2015-06-17
Edwards Lifesciences IntraClude Intra-Aortic Occlusion Device Recalled for Potential Damage
Edwards Lifesciences is recalling IntraClude Intra-Aortic Occlusion Devices due to potential damage near the hub that may cause blood leakage.
Product
Edwards Lifesciences IntraClude Intra-Aortic Occlusion Device, model number ICF100, 10.5 Fr (3.5 mm) x 39.4" (100 cm) ThruPort System. Packaged sterile and non-pyrogenic in a sealed, peel-type pouch For use in patients undergoing cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1719-2015·2015-06-17
Elekta Recalls Leksell GammaPlan Software Due to Memory Corruption
Elekta is recalling 10 units of Leksell GammaPlan 10.2 software because memory can become corrupted when creating a fused study via drag and drop.
Product
Laksell GammaPlan, a computer based dose planning system specifically designed for use with Leksell Gamma Knife, radiation therapy treatment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1768-2015·2015-06-17
Philips Brilliance iCT UPS Accessory Devices Recalled for Battery Acid Leakage
Philips Medical Systems is recalling Brilliance iCT UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Product
Brilliance iCT (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1774-2015·2015-06-17
Philips FORTE UPS Accessory Devices Recalled for Battery Acid Leakage Risk
Philips Medical Systems is recalling 10 FORTE Uninterruptible Power Supply (UPS) accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Product
FORTE (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1741-2015·2015-06-17
Biomet Recalls Unilateral External Fixation Ankle Clamps Due to Assembly Error
Biomet, Inc. is recalling 19 unilateral external fixation ankle clamps because they were assembled incorrectly. The defect may prevent full range of motion and cause the pin to loosen from the bone.
Product
Unilateral external fixation ankle clamp Product Usage: Unilateral external fixation for use treatment of bone conditions amenable to treatment by use of external fixation modality
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1725-2015·2015-06-17
Abbott Alkaline Wash Recall Due to Cap Leaking and Crystallization
Abbott Laboratories is recalling Alkaline Wash cleaning solution for Abbott Architect analyzers due to product leaking from the cap and crystallization around the cap.
Product
Alkaline Wash, List number 9D31-20, a cleaning solution used by the Abbott Architect analyzers. It is supplied in 500 mL bottles and contains NaOCl, NaOH, and KOH. It is shipped and stored at room temperature and is shipped ready to use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1729-2015·2015-06-17
Ortho-Clinical Diagnostics Recalls VITROS Urine Assay Data Disks
Ortho-Clinical Diagnostics is recalling VITROS Urine Assay Data Disks because a software error may allow samples requiring acidified pretreatment to be metered from the same container as those requiring no pretreatment.
Product
Assay Data Disk (ADD), All DRV versions that support product within expiry dating Automates pre-analytical and post-analytical sample and data management for in vitro diagnostic use. VITROS Urine Assays: VITROS Calcium (Ca), Magnesium (Mg), and Phosphorus (Phos) requires…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1116-2015·2015-06-17
Valeant Recalls Nifedipine Extended-Release Tablets Due to Dissolution Failures
Valeant Pharmaceuticals is recalling Nifedipine Extended-Release Tablets, 90 mg, because some lots failed dissolution specifications.
Product
Nifedipine Extended-Release Tablets, USP, 90 mg, 100 Tablet Bottles, Rx Only. Manufactured for: Teva Pharmaceuticals USA Sailorsville, PA 13960. Manufactured in Canada By: Valeant Pharmaceuticals International, Inc. Steinbach, MB R5G 127 Canada. NDC: 0093-2059-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1129-2015·2015-06-17
Akorn Recalls Hydroxyzine Hydrochloride Oral Solution Due to Impurity Failures
Akorn, Inc. is recalling 424,174 bottles of Hydroxyzine Hydrochloride oral solution because the product failed impurities and degradation specifications.
Product
Hydroxyzine Hydrochloride, oral solution, 10 mg per 5 mL, 16 fl oz (473 ml) bottle, Rx only, Manufactured for KVK-Tech, Inc., Newtown, PA by Hi-Tech Pharmacal Co., Inc., Amityville, NY, NDC 10702-0052-16
Category
Drug
Distribution
Distributed nationwide
ModerateUSDA FSIS·093-2015·2015-06-17
Pinnacle Foods Recalls Swanson Turkey Dinners for Undeclared MSG
Pinnacle Foods is recalling approximately 668,316 pounds of Swanson Stuffing Baked Turkey dinners because the product contains monosodium glutamate (MSG) that is not declared on the label.
Product
Recall Notification Report 093-2015 (Poultry Products )
Category
Food
Distribution
Distributed nationwide