State

US Virgin Islands product recalls

73,219 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 177
Critical: 12
Severe: 30
Most recent: 2026-09-23

Of the 177 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 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17901–17925 of 73396

HighFDA (Devices)·Z-0720-2023·2022-12-21
Cordis Angiographic Catheter Extensions Recalled for Male Connector Separation Risk
Cordis angiographic catheter extensions may experience separation at the male connector during use. Approximately 2,915 US units were distributed; users should verify affected lot numbers.
Product
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0475-2023·2022-12-21
Surgical microscope power supply may overheat and cause unexpected shutdown
Leica Microsystems is recalling 43 Proveo 8 surgical microscopes nationwide due to a potential power supply defect that may cause device overheating and unexpected shutdown during use.
Product
Leica MICROSYSTEMS Proveo 8, Part Number 10449058, surgical microscope system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0506-2023·2022-12-21
General Surgery Procedure Kit Recalled for Sterility Concerns
Stradis Medical is recalling surgical procedure kits with potentially incomplete outer bag seals that may compromise sterility. The recall affects 35 units distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, PROCEDURE KIT, Item No.570-1508, general surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2023·2022-12-21
Single-shot epidural kits recalled due to incomplete outer bag sealing
Stradis Medical is recalling 80 Henry Schein single-shot epidural kits due to potentially incomplete outer bag sealing that could compromise sterility. The recall affects units distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, SINGLE SHOT EPIDURAL, Item No.570-3089
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0538-2023·2022-12-21
Stradis Healthcare Thoracic Surgery Kits Recalled for Sterility Risk
Thoracic Phleb procedure kits from Stradis Healthcare are being recalled due to incomplete outer bag sealing during manufacturing, which may compromise kit sterility.
Product
STRADIS HEALTHCARE, Thoracic Phleb, Item No.682-1228,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0514-2023·2022-12-21
ENT Surgical Kits Recalled for Potential Sterility Loss
Stradis Medical is recalling HENRY SCHEIN ENT surgical kits distributed nationwide due to defective outer bag sealing that may compromise sterility. Affected kits were distributed across the US and Canada.
Product
HENRY SCHEIN, ENT SET UP PACK, Item No.570-2742
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0493-2023·2022-12-21
Stradis Healthcare Dental Implant Trays Recalled Due to Incomplete Sealing
Stradis Healthcare is recalling dental implant trays with incomplete outer bag seals that may compromise sterility. Affected units were distributed in the US and Canada.
Product
STRADIS HEALTHCARE, Implants, Item No.41015NSI, dental tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0508-2023·2022-12-21
Surgical Procedure Trays Recalled for Potential Sterility Breach
Stradis Medical recalls surgical procedure trays due to incomplete outer bag sealing that may compromise sterility. The affected products were distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, Basin Set, Item No.570-1803
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0548-2023·2022-12-21
Stradis Healthcare Surgical Procedure Kits Recalled for Incomplete Sealing
Stradis Medical recalls Vein & Laser surgical procedure kits due to incomplete outer bag sealing that may compromise sterility. The recall affects 10 units distributed in the US and Canada.
Product
STRADIS HEALTHCARE, Vein & Laser, Item No.682-334R1,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0084-2023·2022-12-21
Homeopathic Calendula Oil Recalled for Manufacturing Practice Violations
Atlantic Management Resources voluntarily recalls Menastil homeopathic calendula oil due to cGMP deviations. The 26 bottles (Lot A-01) were distributed nationwide and to Australia.
Product
Menastil, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233-711-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0094-2023·2022-12-21
Lacosamide oral solution recalled for failed excipient specifications
Camber Pharmaceuticals is recalling specific lots of Lacosamide oral solution due to out-of-specification p-Hydroxybenzoic Acid content. The recall affects multiple lot numbers distributed nationwide.
Product
LACOSAMIDE — LACOSAMIDE (LACOSAMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0467-2023·2022-12-21
NexGen Option Stemmed Tibial Knee Component Recalled for Higher Revision Rates
Zimmer Biomet is recalling NexGen Option Stemmed Tibial knee components (2,092 units) due to clinically significant higher revision rates when used with specific femoral components. The voluntary recall prevents future implantation with these problematic combinations.
Product
NexGen Option Stemmed Tibial Component Size 4, Item Number 00-5986-037-02
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0716-2023·2022-12-21
Siemens Allergen Test Kit Recall: False Positive Mold Results
Siemens is recalling IMMULITE 2000 allergen test kits that may produce false positive results for mold allergies in both quality control and patient samples.
Product
IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)- US. Siemens Material Number (SMN): 10708840 For in vitro diagnostic use with the IMMULITE 2000 Systems Analyzers for the quantitative measurement of allergen-specific IgE in human serum, as an aid in…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0496-2023·2022-12-21
Dental Procedure Trays Recalled for Incomplete Outer Bag Seal
STRADIS HEALTHCARE dental procedure trays may have incompletely sealed outer bags that could compromise sterility. The recall affects units distributed nationwide in the US and Canada.
Product
STRADIS HEALTHCARE, Custom Pack, Item No.41213ATCP, dental
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0082-2023·2022-12-21
FDA recalls Neuroquell Calendula Oil homeopathic drug for manufacturing deviations
The FDA has recalled Neuroquell Calendula Oil, a homeopathic drug, due to manufacturing practice violations. The voluntary recall affected 51 bottles distributed nationwide and in Australia.
Product
Neuroquell, A Homeopathic Drug, Calendula Oil, packaged in1/8 Fl. oz. (3.5 g) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233712-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0081-2023·2022-12-21
Drug Neuroquell Plus Calendula Oil Recalled for Manufacturing Deviations
Neuroquell Plus, a homeopathic calendula oil drug, has been voluntarily recalled due to current good manufacturing practice (cGMP) deviations. The recall affects 461 bottles distributed nationwide and in Australia.
Product
Neuroquell Plus, Advanced Formula, A Homeopathic Drug, Calendula Oil packaged in 0.22 Fl. oz. (6.6 mL) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233712-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0083-2023·2022-12-21
Drug Recall: ProSirona Homeopathic Calendula Oil Manufacturing Deviations
ProSirona Homeopathic Calendula Oil (Lot B-02) is being recalled because the manufacturer failed to follow Current Good Manufacturing Practice standards. The voluntary recall affects products distributed nationwide and in Australia.
Product
ProSirona, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Dist. by: Endometriosis Assoc. Inc. (International), Mfg. by Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233-712-01.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V943000·2022-12-20
New Flyer Transit Buses Recalled for Steering Column Defect
New Flyer is recalling 746 transit buses because a loose steering column connection may cause loss of steering, increasing crash risk.
Product
NEW FLYER — NEW FLYER XDE35, XN40, XT40, XT60
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V944000·2022-12-20
2022-2023 BMW iX and i4 Recalled for Battery Software Electrical Power Loss
BMW recalls certain 2022-2023 iX, i4, and 2023 i7 models due to a high voltage battery ECU software issue that may interrupt electrical power and suddenly disable drive power.
Product
BMW — BMW IX, I7, I4
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V942000·2022-12-19
2023 BMW X5 driver seat backrest fastener defect recall
BMW is recalling certain 2023 X5 models because one of four bolts connecting the driver's seat backrest to the frame may not have been correctly installed, potentially preventing proper occupant restraint during a crash.
Product
BMW — BMW X5
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V939000·2022-12-16
Peterbilt 320 and 520 Refuse Trucks Recalled for Suspension Defect
PACCAR is recalling 2015-2023 Peterbilt 320 and 520 refuse trucks because suspension brackets may fail, causing axle instability and increasing crash risk.
Product
PETERBILT — PETERBILT 320, 520
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V934000·2022-12-16
Lightning eMotors Recalls FE4 Vehicles for Battery Power Loss Risk
Lightning eMotors is recalling 2021-2022 FE4-129 vehicles because the high-voltage battery may lose traction power or fail to start, increasing crash risk.
Product
LIGHTNING EMOTORS — LIGHTNING EMOTORS FE4
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V936000·2022-12-16
Mercedes-Benz Recalls GLE and GLS Models for Steering Screw Defect
Mercedes-Benz is recalling 2021-2022 GLE and GLS vehicles because a steering coupling locking screw may loosen, potentially causing a loss of steering control.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG GLE63, GLS 450 4MATIC, AMG GLE53, GLE 450
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V937000·2022-12-16
Mercedes-Benz Recalls 2022 AMG G63 Due to Rear Axle Defect
Mercedes-Benz is recalling 278 2022 AMG G63 vehicles because the rear axle differential housing may crack or break, potentially causing loss of control.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG G63
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V941000·2022-12-16
Hyundai Recalls 2021 Kona Electric Vehicles Due to EPCU Coolant Leak Risk
Hyundai is recalling 2021 Kona Electric vehicles because a defective Electric Power Control Unit may leak coolant, potentially causing a loss of drive power and increasing crash risk.
Product
HYUNDAI — HYUNDAI KONA ELECTRIC
Category
Vehicle
Distribution
Distributed nationwide