State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42401–42425 of 73919

HighFDA (Devices)·Z-2695-2017·2017-07-19
St. Jude Medical Recalls Infinity 7 Implantable Pulse Generators
St. Jude Medical is recalling 373 Infinity 7 Implantable Pulse Generators because exposure to monopolar electrosurgical devices may cause a loss of neuromodulation therapy.
Product
Infinity 7, Implantable Pulse Generator, REF 6662, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2679-2017·2017-07-19
ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption
ICU is recalling Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2694-2017·2017-07-19
St. Jude Medical Recalls Infinity 5 Implantable Pulse Generators
St. Jude Medical is recalling 54 Infinity 5 Implantable Pulse Generators due to a risk of therapy loss if exposed to monopolar electrosurgical devices.
Product
Infinity 5, Implantable Pulse Generator, REF 6661, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2731-2017·2017-07-19
O-Two Medical Recalls Burn Relief Dressings Due to Sterilization Concerns
O-Two Medical Technologies is voluntarily recalling specific lots of Burn Relief hydrogel dressings because there is a lack of evidence validating the sterilization dose, posing a potential contamination risk.
Product
Burn Relief¿, MODEL #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200, CATALOG #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200 --- DRESSING,WOUND,HYDROGEL W/OUT DRUG AND/OR BIOLOGIC. --- Burn Relief¿ products are self-cooling, non-adhering and are intended to be used on 1st and 2nd…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2696-2017·2017-07-19
St. Jude Medical Recalls Infinity 7 Implantable Pulse Generators
St. Jude Medical is recalling 40 Infinity 7 Implantable Pulse Generators because exposure to monopolar electrosurgical devices during medical procedures may cause a loss of neuromodulation therapy.
Product
Infinity 7, Implantable Pulse Generator, REF 6663, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0973-2017·2017-07-19
Baxter Recalls Sodium Chloride Injection Bags Due to Sterility Concerns
Baxter Healthcare is recalling 295,200 bags of 0.9% Sodium Chloride Injection due to a lack of assurance of sterility and potential for leaking.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2677-2017·2017-07-19
ICU Recalls 71 Plum A+ Infusion Systems Due to Battery Error
ICU is recalling 71 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2681-2017·2017-07-19
ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption
ICU is recalling 21,703 Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2676-2017·2017-07-19
ICU Recalls Plum A+ Infusion Systems Due to Battery-Related Therapy Interruption
ICU is recalling 10,609 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting patient therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2675-2017·2017-07-19
ICU Recalls 180 Plum A+ Infusion Systems Due to Battery Issues
ICU is recalling 180 Plum A+ Infusion Systems because battery issues may cause an E321 error code and interrupt therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2709-2017·2017-07-19
Toshiba XARIO 200 Ultrasound System Recalled for Incorrect Velocity Trace Values
Toshiba American Medical Systems is recalling XARIO 200 diagnostic ultrasound systems because the Continuous Trace method may display incorrect velocity trace values.
Product
XARIO 200 TUS-X200 diagnostic ultrasound system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2713-2017·2017-07-19
Pentax Video Duodenoscope Recall for Surface Soiling Investigation
Pentax of America Inc. issued a field correction for two Video Duodenoscope models to investigate surface soiling on the suction cylinder and distal cap.
Product
Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and therapeutic access to, the biliary tract via the upper GI tract. This anatomy includes, but is not restricted to, the organs; tissues; and subsystems: esophagus…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2682-2017·2017-07-19
ICU Recalls Plum A+ Infusion Systems Due to Battery Error
ICU is recalling 7,351 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2680-2017·2017-07-19
ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption
ICU is recalling 7,848 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting patient therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2678-2017·2017-07-19
ICU Recalls 214 Plum A+ Infusion Systems Due to Battery Error
ICU is recalling 214 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2691-2017·2017-07-19
St. Jude Medical Recalls Proclaim 5 Elite Implantable Pulse Generators
St. Jude Medical is recalling 8,780 Proclaim 5 Elite implantable pulse generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.
Product
Proclaim 5 Elite, implantable Pulse Generator, REF 3660, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2707-2017·2017-07-19
Merge Healthcare Recalls Schiller PB 1000 Patient Data Module
Merge Healthcare is recalling 555 Schiller PB 1000 Patient Data Modules because the analog output may not accurately reflect the pressure waveform used for fractional flow reserve calculations.
Product
The Schiller PB 1000, also known as Merge Hemo Patient Data Module (PDM), a major component of the Merge Hemo software.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2466-2017·2017-07-19
3CS Organics Recalls Unapproved Holle Goat Milk Infant Formula
3CS Organics LLC is recalling Holle goat milk infant formula products that are not FDA approved and lack English labeling.
Product
HOLLE Bio Lait Pour Nourrissons Au Lait De Chevre, Zuigelingenmelk OP Geitenmelbasis, 1, 400g (4/case), HOLLE Bio-Flogemilch Auf Ziegenmilchbasis, 1, 400g (4/case), HOLLE Bio-Folgenmilch Auf Ziegenmilchbasis, 3, 400g (4/case), HOLLE Bio-Folgemich, 2, 600g (3bx/case), HOLLE…
Category
Food
Distribution
Distributed nationwide
HighNHTSA·17V459000·2017-07-19
Carry-On Trailer Recalls 2017 Models Due to Electric Brake Defect
Carry-On Trailer is recalling 2017 Utility, Dump, and Enclosed trailers because a faulty breakaway box light may cause the circuit board to fail, increasing crash risk.
Product
CARRY-ON TRAILER — CARRY-ON TRAILER ENCLOSED, UTILITY, DUMP
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2732-2017·2017-07-19
Nova Biomedical Stat Profile Prime Analyzer Software Recall
Nova Biomedical is recalling Stat Profile Prime Analyzers because a software defect could cause scheduled quality control tests to overwrite pending patient results.
Product
Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Stat Profile Prime ABG Analyzer PN 53655 Stat Profile Prime ABG Analyzer with Scanner PN 52856 Stat Profile Prime CCS Analyzer PN 53656 Stat Profile Prime CCS Analyzer with Scanner PN 53657 Stat Profile Prime…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2693-2017·2017-07-19
St. Jude Medical Recalls Infinity 5 Implantable Pulse Generators
St. Jude Medical is recalling 443 Infinity 5 Implantable Pulse Generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.
Product
Infinity 5, Implantable Pulse Generator, REF 6660, Rx only, STERILE EO, Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2683-2017·2017-07-19
ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption
ICU is recalling 363,892 Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting patient therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2710-2017·2017-07-19
Toshiba APLIO 300 Ultrasound Systems Recalled for Incorrect Velocity Trace Display
Toshiba is recalling 90 APLIO 300 diagnostic ultrasound systems because they may display incorrect velocity trace values when using the Continuous Trace method.
Product
APLIO 300 TUS-A300 diagnostic ultrasound system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2692-2017·2017-07-19
St. Jude Medical Recalls Proclaim 7 Elite Implantable Pulse Generators
St. Jude Medical is recalling 9,529 Proclaim 7 Elite implantable pulse generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.
Product
Proclaim 7 Elite, Implantable Pulse Generator, REF 3662, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2712-2017·2017-07-19
Toshiba APLIO i-series Ultrasound Systems Recalled for Incorrect Velocity Readings
Toshiba is recalling 28 APLIO i-series diagnostic ultrasound systems because they may display incorrect velocity values when using the Continuous Trace method.
Product
APLIO i-series: a) APLIO i700 TUS AI700 b) APLIO i800 TUS AI800 diagnostic ultrasound system
Category
Medical Device
Distribution
Distributed nationwide