State

US Virgin Islands product recalls

73,198 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 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15526–15550 of 73375

HighFDA (Devices)·Z-1988-2023·2023-06-28
Olympus QUICKCLIP PRO hemostatic clips recalled for deployment failures
Olympus is recalling QUICKCLIP PRO hemostatic clips due to deployment failures that could prevent proper function during GI procedures. Clip arms may fail to operate or clips may detach prematurely from tissue.
Product
Single Use Repositionable Clip QUICKCLIP PRO 165CM 5/BX- Intended for hemostatic metal clip for the GI Tract Catalog Number: HX-202LR.B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1992-2023·2023-06-28
Draeger Resuscitaire Warmer Scale May Display Inaccurate Weight Values
Draeger Medical Systems is recalling 936 units of Softbed Resuscitaire and Birthing Room Warmer models with optional scales that may display inaccurate weight readings, affecting clinical care for newborns.
Product
Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale [Model(s): RW82VHA-1, RW82VHA-1C, RW82VHA-1D, RW82-1, RW82-1C, RW82-1D, WBR82-1 and WBR82-1C]
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1990-2023·2023-06-28
Hemostatic Clip Device Recalled Due to Deployment Failures
Olympus recalls QUICKCLIP PRO hemostatic clips nationwide due to reported malfunction during clinical procedures, where clips fail to open, close, or detach from tissue as intended.
Product
Single Use Repositionable Clip QUICKCLIP PRO 230CM 5/BX- Intended for hemostatic metal clip for the GI Tract Catalog Number: HX-202UR.B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1978-2023·2023-06-28
Hemospray Endoscopic Hemostat Recall Due to Endoscope Adhesion Risk
Wilson-Cook Medical's Hemospray Endoscopic Hemostat is being recalled because the powder can adhere to the endoscope, potentially making it difficult to remove the instrument from the patient.
Product
Hemospray Endoscopic Hemostat: Reference Part Numbers: a) HEMO-7, REF G56572; b) HEMO-7-EU, REF G24663;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V450000·2023-06-28
Kidron Refrigerated Truck Bodies Recalled for Fire Risk
ST Engineering Hackney is recalling 2011-2021 Kidron refrigerated truck bodies because a centrifugal clutch may overheat and break, creating a fire hazard.
Product
KIDRON — KIDRON REFRIGERATED BODIES
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1718-2023·2023-06-28
Medtronic Implantable Cardiac Defibrillators Risk Reduced Energy During Therapy
Medtronic implantable cardiac defibrillators may deliver reduced or no energy during defibrillation therapy due to a feedthrough defect. Approximately 11,239 devices distributed worldwide are affected.
Product
ICD-DR DDMD3D4 PRIMO MRI, Model Number DDMD3D4; Implantable Cardioverter Defibrillators
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1979-2023·2023-06-28
Hemospray Endoscopic Hemostat Recalled for Powder Adhesion Risk
Wilson-Cook Medical is recalling Hemospray Endoscopic Hemostat units (14,877 devices, US and worldwide distribution) because powder can adhere to the endoscope tip, potentially making removal difficult or impossible.
Product
Hemospray Endoscopic Hemostat: Reference Part Numbers: a) HEMO-10, REF G21049; b) HEMO-10-EU, REF G21346
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1987-2023·2023-06-28
Olympus QUICKCLIP PRO hemostatic clips recalled for deployment failures
Olympus is recalling 340 QUICKCLIP PRO hemostatic clips used in gastrointestinal endoscopy due to reports of deployment failures during procedures, including clips that fail to open, close, or detach properly.
Product
Single Use Repositionable Clip QUICKCLIP PRO 165 CM 10/BX- Intended for hemostatic metal clip for the GI Tract Catalog Number: HX-202LR.A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1712-2023·2023-06-28
Implantable Cardioverter Defibrillators Recalled for Rare Therapy Delivery Failure
Certain Medtronic implantable defibrillators may fail to deliver high voltage therapy in rare cases due to a manufacturing defect. The recall affects approximately 61,404 units distributed worldwide.
Product
ICD-DR DDMB1D4 EVERA MRI XT IS-1/DF4 US, Model Number DDMB1D4; Implantable Cardioverter Defibrillators
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V452000·2023-06-28
Certain 2021–2025 Lion LionC School Buses Electrical Hardware Recall
Lion Electric is recalling 2021–2025 LionC school buses due to loose electrical hardware that could cause short circuits and loss of steering or braking power. Contact Lion customer service at 1-855-546-6706 for free replacement.
Product
LION — LION LIONC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1743-2023·2023-06-28
Implantable Defibrillators Recalled for Potential High-Voltage Therapy Failure
Medtronic CRT-D and ICD devices with a specific feedthrough may fail to deliver high-voltage therapy. The FDA Class I recall affects multiple lot numbers due to rare potential for reduced or no energy output during critical treatment.
Product
CRT-D DTBB1Q1 VIVA QUAD S IS4/DF1 US, Model Number DTBB1Q1; Implantable Cardioverter Defibrillators
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V449000·2023-06-28
2022-2023 BMW I4 Recalled for High Voltage Battery Charging Unit Failure
BMW recalls certain 2022-2023 I4, iX, and i760 models due to a defective high voltage battery charging unit that may not have been properly assembled, potentially causing engine stall while driving.
Product
BMW — BMW IX, I4, 760I
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1754-2023·2023-06-28
Implantable Cardiac Defibrillators May Deliver Reduced Energy Output
Certain Medtronic cardiac defibrillators may deliver reduced or no energy during high voltage therapy. No injuries or deaths have been reported.
Product
CRTD DTMA1D4 CLARIA MRI US DF4, Model Number DTMA1D4; Implantable Cardioverter Defibrillators
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1981-2023·2023-06-28
KARL STORZ sterilization trays recalled for inadequate model-specific instructions
FDA recalls KARL STORZ sterilization trays (4,386 units) because instructions lacked model-specific details and sterilization modality information, risking improper device sterilization.
Product
KARL STORZ Radel Sterilization Trays, Models: 27717A, 27717B, 39301A, 39301C, 39231XA, 39301C1, 39311A, 39317A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0877-2023·2023-06-28
Glycopyrrolate Tablets Recalled Due to Failed Impurities and Degradation Specifications
Aurolife Pharma has recalled Glycopyrrolate Tablets (1 mg) nationwide due to failed impurity and degradation specifications. Affected lot 01421038A1 expires May 2023.
Product
GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1980-2023·2023-06-28
V-Sign Sensor 2 May Experience Out-of-Box Failure Due to Software Configuration
The V-Sign Sensor 2, a component of the Sentec Digital Monitoring System, may fail out of the box due to improper software mode configuration after recalibration. Approximately 11 units were distributed in select U.S. states.
Product
V-Sign Sensor 2, REF VS-A/P/N, a component of Sentec Digital Monitoring System (model SDMS).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1993-2023·2023-06-28
HeartWare Ventricular Assist Device Monitor logfile processing failure
Heartware, Inc. is recalling 19 HeartWare Ventricular Assist Device System monitors (Model 1521 variants) because recently updated units cannot process downloaded logfiles in the Autologs web portal.
Product
HeartWare Ventricular Assist Device System. a) Monitor 1521US Explore Tech, b) Monitor 1521GB Explore Tech, c) Monitor 1521IL Explore Tech, d) Monitor 1521DE Explore Tech
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1977-2023·2023-06-28
FDA Recalls MiSeq Dx Instruments for Software Cybersecurity Vulnerability
Illumina recalls 740 MiSeq Dx sequencing instruments due to a software cybersecurity vulnerability affecting the Universal Copy Service component. No patient harm reported.
Product
MiSeq Dx Instrument, Catalog # M70101, containing Universal Copy Service (UCS) software.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·23V451000·2023-06-27
Lion Electric Recalls 2021-2025 Lion6 and Lion8 Vehicles for Electrical Defect
Lion Electric is recalling 2021-2025 Lion6 and Lion8 vehicles because loose hardware may cause a short circuit, leading to loss of power and increased crash risk.
Product
LION — LION LION8, LION6
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V447000·2023-06-27
2022-2024 Thor Motor Coach motorhomes recalled for detachable bike racks
Thor Motor Coach is recalling certain 2022-2024 Tranquility and 2022-2023 Sanctuary motorhomes because the R-bike rack arms may fracture and detach, increasing crash risk.
Product
THOR MOTOR COACH — THOR MOTOR COACH TRANQUILITY, SANCTUARY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V448000·2023-06-27
Lion LionC School Buses Surge Tank Defect May Cause Steering and Braking Loss
Lion Electric is recalling 2019-2025 LionC school buses due to a surge tank support bracket defect. The tank may crack the firewall and damage high-voltage cables, potentially causing loss of steering assistance, drive power, and braking ability.
Product
LION — LION LIONC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23E048000·2023-06-27
Eagle Eyes Recalls Aftermarket Headlights for Peterbilt 389 Vehicles
Eagle Eyes is recalling specific aftermarket headlights for Peterbilt 389 vehicles because they may not provide sufficient light output, potentially reducing visibility and increasing crash risk.
Product
EXTERIOR LIGHTING:HEADLIGHTS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V443000·2023-06-26
Porsche Recalls Macan and Panamera Models for Seat Belt Anchor Defect
Porsche is recalling certain 2016-2020 Macan and Panamera models because a rear seat belt anchor screw may not be tightened properly, increasing injury risk in a crash.
Product
PORSCHE — PORSCHE MACAN S, MACAN, MACAN TURBO, PANAMERA TURBO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V444000·2023-06-26
Fuel Pump Failure Risk in 2021-2023 Freightliner and Mercedes-Benz Sprinters
Daimler Vans USA is recalling 2021-2023 Freightliner Sprinter and Mercedes-Benz Sprinter and Metris vehicles due to a fuel pump defect. The pump may shutdown, causing loss of drive power and increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 1500, METRIS, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V446000·2023-06-26
2022–2023 Porsche 911 GT3 Rear Spoiler Control Software Error
A software error in the rear spoiler control unit may cause brake lights to activate simultaneously on 2022–2023 Porsche 911 GT3 vehicles, potentially confusing other drivers.
Product
PORSCHE — PORSCHE 911 GT3
Category
Vehicle
Distribution
Distributed nationwide