State

US Virgin Islands product recalls

72,940 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: 2026-09-09

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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3476–3500 of 73117

HighFDA (Drugs)·D-0295-2026·2026-01-28
Icosapent ethyl capsules recalled as subpotent after capsule contents leaked
Zydus Pharmaceuticals is recalling 22,896 bottles of Icosapent Ethyl capsules, 1 gram, because oxidation caused by leakage of the capsule contents has left them subpotent.
Product
Icosapent Ethyl capsules, 1 gram, 120-count bottles, Rx only, Manufactured by: Softgel Healthcare Pvt. Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1592-07
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1112-2026·2026-01-28
PET scanners recalled over a streaking artifact in clinical images
GE HealthCare is recalling 364 Omni Legend PET systems because an intermittent issue can produce a streaking artifact in PET clinical scan images.
Product
GE Healthcare Omni Legend, sold under the following names: OMNI Legend 16, Omni Legend 21, OMNI Legend 32, Omni Legend PET Gantry 16cm - MEA, Omni Legend PET Gantry 16cm Haifa LM, Omni Legend PET Gantry 16cm Mobile, Omni Legend PET Gantry 21cm - BJ for Global, Omni Legend PET
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1122-2026·2026-01-28
Robotic guidance systems recalled over incorrect surgical instrument positioning errors
Mazor Robotics is recalling 549 Mazor X robotic guidance systems over software errors that can result in incorrect surgical instrument positioning during spinal surgery.
Product
Mazor X robotic guidance system REF: TPL0059
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1124-2026·2026-01-28
Angiographic inflation devices recalled over handles that may detach
Merit Medical Systems is recalling 173,645 units of the Allwell Inflation Device because the inflation device handle may detach from the syringe during a procedure.
Product
Allwell Inflation Device, for angiographic use REF: IS-30-A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1125-2026·2026-01-28
Waste management vascular trays recalled over inflation handles that may detach
Merit Medical Systems is recalling 864 units of its Custom Waste Management Kit Vascular Tray because the inflation device handle may detach from the syringe during a procedure.
Product
Merit Medical , Custom Waste Management Kit Vascular Tray REF: K10T-05261
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V049000·2026-01-28
Toyota Prius models recalled for unexpected rear door opening risk
Toyota is recalling certain 2023–2026 Prius and Prius Prime models because water may enter the rear door switch, causing an unlocked door to open unexpectedly while driving. This increases injury risk.
Product
TOYOTA — TOYOTA PRIUS PLUG-IN HYBRID, PRIUS PRIME, PRIUS
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0291-2026·2026-01-28
Diclofenac topical gel recalled after failing pH specifications
Cipla USA is recalling 92,376 tubes of Diclofenac Sodium Topical Gel 1% after the batch failed pH specifications.
Product
DICLOFENAC SODIUM — DICLOFENAC SODIUM (DICLOFENAC SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1152-2026·2026-01-28
M3B vital signs monitors recalled over potential cybersecurity issues
Edan Diagnostics is recalling 354 units of its M3B Vital Signs Monitor after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: M3B Product Description: M3B Vital Signs Monitor is a patient monitoring device providing the patient with a continuous vital physiological monitoring of arterial blood oxygen saturation (SpO2), Pulse Rat
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1132-2026·2026-01-28
Long distal radius plates recalled over an incorrect thread orientation
Tyber Medical is recalling 64 units VOLT Wrist Treatment System distal radius plates because the supplier manufactured anatomical left plates with an incorrect thread orientation.
Product
Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/14Shaft/Left/Std/186mm Model/Catalog Number: 02.426.691S Product Description: 2 Column Distal Radius Plate - 6 Head, 14 Shaft, Standard Left - 186mm Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1137-2026·2026-01-28
TRAM powered lift devices recalled over potential strap fraying
Community Products is recalling 3,238 units of the Rifton TRAM over potential fraying on the body support strap.
Product
Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1149-2026·2026-01-28
iX series patient monitors recalled over potential cybersecurity issues
Edan Diagnostics is recalling 379 units of its Patient Monitor models iX10, iX12 and iX15 after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iX10, iX12, iX15 Product Description: The iX series Patient Monitors including iX10, iX12, iX15 can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1155-2026·2026-01-28
Telemetry transmitters recalled over potential cybersecurity issues flagged by FDA
Edan Diagnostics is recalling 1,457 units of its iT20 Telemetry Transmitter after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Telemetry Transmitter Model/Catalog Number: iT20 Product Description: iT20 collects physiological parameters by ECG cables and SpO2 sensors, then achieves data analyzing and processing. After that, data will be sent to MFM-CMS via Wi-Fi. The para
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1120-2026·2026-01-28
Plum Solo pumps recalled over hard limit messages blocking flush programming
ICU Medical is recalling the Plum Solo Precision IV Pump because clinicians may receive an Upper or Lower Hard Limit violation message that prevents a piggyback flush from being programmed.
Product
ICU Medical Plum Solo Precision IV Pump, List Numbers: 400010401 (US), 400011001 (Philippines)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1139-2026·2026-01-28
Gait training devices recalled over potential fraying on the body support strap
Community Products is recalling 470 units of the Rifton E-Pacer gait training device over potential fraying on the body support strap.
Product
Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1150-2026·2026-01-28
Central monitoring systems recalled over potential cybersecurity issues flagged by FDA
Edan Diagnostics is recalling 195 units of its MFM-CMS Central Monitoring System after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog Number: MFM-CMS Product Description: MFM-CMS is a central monitoring system product, which can connect and manage information from EDAN medical devices. MFM-CMS offers central management for monitoring info
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1146-2026·2026-01-28
Elite V series patient monitors recalled over potential cybersecurity issues
Edan Diagnostics is recalling 342 units of its Patient Monitor models elite V5, elite V6 and elite V8 after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: elite V5, elite V6, elite V8 Product Description: V series Patient Monitor including elite V5, elite V6 and elite V8 which can perform long-time continuous monitoring of multiple physiological parameters. Als
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1156-2026·2026-01-28
Patient information centers recalled over a patch changing notification filters
Philips North America is recalling 146 Patient Information Center iX units because a software patch modifies Mobile Event Notification filter settings without any indication to the user.
Product
Patient Information Center iX; Software Version Number: 4.5.0
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1154-2026·2026-01-28
iM8 series patient monitors recalled over potential cybersecurity issues
Edan Diagnostics is recalling 3,141 units of its Patient Monitor models iM8, iM8A and iM8B after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM8, iM8A, iM8B Product Description: iM8 Series Patient Monitor can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing, displaying, analyzing and cont
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1144-2026·2026-01-28
iM3s series vital signs monitors recalled over potential cybersecurity issues
Edan Diagnostics is recalling 136 units of its Vital Signs Monitor models iM3s, iM3As, iM3Bs and iHM3s after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: iM3s, iM3As, iM3Bs, iHM3s Product Description: The iM3s series vital signs monitors including iM3s/iM3As/iM3Bs/iHM3s are intended to be used for measuring, storing, reviewing of, and generating prompts fo
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1141-2026·2026-01-28
Fetal and maternal monitors recalled over potential cybersecurity issues
Edan Diagnostics is recalling 3,518 units of its Fetal & Maternal Monitor models F6, F9, F6 Express and F9 Express after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Fetal & Maternal Monitor Model/Catalog Number: F6, F9, F6 Express, F9 Express Product Description: The devices are bedside fetal and maternal monitors, which are used to monitor the physiological parameters of pregnant women including the fetus f
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1138-2026·2026-01-28
iM20 patient monitors recalled over potential cybersecurity issues flagged by FDA
Edan Diagnostics is recalling 377 units of its iM20 Patient Monitor after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training. The low base variant includes smaller casters and lower base frame so that th
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1118-2026·2026-01-28
Plum Duo infusion pumps recalled over blocked piggyback flush programming
ICU Medical is recalling the Plum Duo Infusion Pump because clinicians may receive an Upper or Lower Hard Limit violation message that prevents a piggyback flush from being programmed.
Product
ICU Medical Plum Duo Infusion Pump, List Numbers: 400020401 (US), 400021001 (Philippines)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1142-2026·2026-01-28
M3 vital signs monitors recalled over potential cybersecurity issues
Edan Diagnostics is recalling 13,934 units of its M3 Vital Signs Monitor after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: M3 Product Description: The Vital Signs Monitor is a portable device intended for use by health care professionals. The monitor could provide the monitoring of physiological parameters such as the non-inv
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1148-2026·2026-01-28
X series patient monitors recalled over potential cybersecurity issues flagged by FDA
Edan Diagnostics is recalling 3,824 units of its Patient Monitor models X8, X10 and X12 after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: X8, X10, X12 Product Description: The X8 X10 X12 Patient Monitor (hereinafter called X series) can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1143-2026·2026-01-28
iM3 vital signs monitors recalled over potential cybersecurity issues
Edan Diagnostics is recalling 11,987 units of its iM3 Vital Signs Monitor after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: iM3 Product Description: The iM3 has three work modes, Monitor, Spot and Round, to measure physiological parameters, including non-invasive blood pressure (NIBP), oxygen saturation of the blood (SpO2), pu
Category
Medical Device
Distribution
Distributed nationwide