State

US Virgin Islands product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27726–27750 of 73754

HighFDA (Devices)·Z-2913-2020·2020-09-09
Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects
Cardinal Health is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect may cause holes and tears at the cuffs.
Product
PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2934-2020·2020-09-09
Siemens Symbia S and T Series SPECT Systems Recalled for Detector Motion
Siemens Medical Solutions is recalling 412 Symbia S and T Series SPECT systems due to a defect that may cause unintended slow motion of the detectors.
Product
Symbia S-Series and Symbia T-Series - Product Usage: Intended use of the device SPECT: To detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2920-2020·2020-09-09
Remel Bordetella pertussis Agglutinating Serum Recalled for False Negative Results
Remel Europe Ltd. is recalling Thermo Scientific Remel Bordetella pertussis Agglutinating Serum because it may produce false negative results for serotypes 1 and 3.
Product
Thermo Scientific Remel Bordetella pertussis Agglutinating Serum Product Number: R30165501, UDI-DI: 05056080501826 - Product Usage: Bordetella antisera are suitable for use in slide agglutination tests to serologically identify Bordetella pertussis and Bordetella parapertussis…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2915-2020·2020-09-09
Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects
Cardinal Health 200, LLC is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect may cause holes and tears at the cuffs.
Product
PROTEXIS Latex Micro Surgical Gloves Size 7.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2935-2020·2020-09-09
CareFusion Recalls BD Alaris EtCO2 Modules Due to Monitoring Interruption Risk
CareFusion 303, Inc. is recalling 680 BD Alaris EtCO2 modules because a component defect may interrupt patient monitoring.
Product
BD Alaris System. The EtCO2 module is a capnograph indicated for continuous, noninvasive monitoring of end tidal carbon dioxide (EtCO2), fractional inspired carbon dioxide (FiCO2) and respiratory rate (RR). The EtCO2 module and disposables are indicated for use with intubated…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2912-2020·2020-09-09
Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects
Cardinal Health is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect could cause holes or tears at the cuffs, compromising barrier protection.
Product
PROTEXIS Latex Micro Surgical Gloves Size 5.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20179·2020-09-09
Cannondale Treadwell Front Racks Recalled Due to Fall Hazard
Cycling Sports Group is recalling front racks for Cannondale Treadwell bicycles because they can detach and cause falls.
Product
Front Racks with Bamboo Trays
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2917-2020·2020-09-09
Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects
Cardinal Health is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect may cause holes and tears at the cuffs.
Product
PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2928-2020·2020-09-09
Stimwave StimQ Peripheral Nerve Stimulator Recalled for Non-Functional Component
Stimwave Technologies is recalling 2,444 StimQ Peripheral Nerve Stimulator Systems because they contain a non-functional component not referenced in product labeling.
Product
StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1569-2020·2020-09-09
AAA Cosmetica Recalls bio aaa Advance Hand Sanitizer Due to CGMP Deviations
AAA Cosmetica is voluntarily recalling 21,228 bottles of bio aaa Advance Hand Sanitizer due to Current Good Manufacturing Practice (CGMP) deviations.
Product
bio aaa Advance Hand Sanitizer Ethyl Alcohol 70%, Unscented, 16.23 Oz (480 mL), Distributed By: Payless Janitorial Corporation 1341 SW 21 Terrance, Fort Lauderdale, Florida Exported By: E. Audicode S.A. de C.V. Manufactured By: AAA Cosmetica S.A. de C.V. UPC 7 502272 12111 5
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1555-2020·2020-09-09
Jaloma Antiseptic Hand Sanitizer Recalled for cGMP Deviations
Laboratorios Jaloma is recalling 211,875 bottles of Jaloma Antiseptic Hand Sanitizer due to current Good Manufacturing Practice (cGMP) deviations.
Product
Jaloma Antiseptic Hand Sanitizer, Ethyl Alcohol 62% with Vitamin E, packaged in a) 16.9 Fl. Oz. (1.06 pint, 500 mL), NDC# 65055-600-02, UPC# 759684515033, b) 4 Fl. Oz.(120 mL), NDC# 65055-600-01, UPC# 75968455026, Laboratorios Jaloma S.A. DE C.V., Aquiles Serdan 438, Z.P. 44380…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2911-2020·2020-09-09
C.A. Greiner HOLDEX Plastic Cannula Recalled for Sample Leakage
C.A. Greiner & Sohne is recalling 390,000 units of HOLDEX Plastic Cannulas (Lot A19073FK) because sample may leak from the sleeve covering the needle.
Product
Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen withdrawal from specimen collection bags or bottles through needleless cannula ports.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2929-2020·2020-09-09
Stimwave StimQ Peripheral Nerve Stimulator System Recalled for Non-Functional Component
Stimwave Technologies is recalling 1,550 StimQ Peripheral Nerve Stimulator Systems because they contain a non-functional component not referenced in product labeling.
Product
StimQ Peripheral Nerve Stimulator System (PNS) Model FR4A-TRL-AO US - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2932-2020·2020-09-09
Stimwave StimQ Peripheral Nerve Stimulator Recalled for Non-Functional Component
Stimwave Technologies is recalling 2,197 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not listed in the product labeling.
Product
StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2872-2020·2020-09-09
GE Healthcare Recalls OEC 9800 and 9900 C-Arms for Dose Display Issues
GE Healthcare is recalling 221 OEC 9800 and 9900 C-Arms because field service engineers changed the dose display to DAP, violating FDA regulations requiring AKR/CAK.
Product
The OEC 9900 C-Arm is designed to provide fluoroscopic and spot-film images of the patient during diagnostic, surgical and interventional procedures. Examples of clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic, vascular, cardiac…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2933-2020·2020-09-09
Stimwave StimQ Peripheral Nerve Stimulator Recalled for Non-Functional Component
Stimwave Technologies is recalling 13 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not listed in the product labeling.
Product
StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-RCV-AO US and 2. FR4A-RCV-A0 EU - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2930-2020·2020-09-09
Stimwave StimQ Peripheral Nerve Stimulator Recalled for Non-Functional Component
Stimwave Technologies is recalling 1,424 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not referenced in product labeling.
Product
StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-TRL-BO US and 2. FR4A-TR-BO - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2931-2020·2020-09-09
Stimwave StimQ Peripheral Nerve Stimulator System Recalled for Non-Functional Component
Stimwave Technologies is recalling six StimQ Peripheral Nerve Stimulator Systems because they contain a non-functional component not referenced in product labeling.
Product
StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1557-2020·2020-09-09
Santa Cruz Recalls Subpotent UltraCruz Hand Sanitizing Gel
Santa Cruz Biotechnology is recalling 14,238 bottles of UltraCruz Hand Sanitizing Gel because the product is subpotent.
Product
UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol), packaged in 3 Fluid Oz./89 mL bottes, Manufactured By Santa Cruz Biotechnology, Inc. 10410 Finnell St. Dallas, TX 75220
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2914-2020·2020-09-09
Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects
Cardinal Health 200, LLC is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect could cause holes and tears at the cuffs.
Product
PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V545000·2020-09-08
Autocar Recalls 2019 Xpeditor Vehicles for Methane Detection Wiring Fire Risk
Autocar is recalling 170 2019 Xpeditor vehicles equipped with factory-installed methane detection systems because inadequate circuit protection may cause the wiring harness to overheat, increasing the risk of a fire.
Product
AUTOCAR — AUTOCAR XPEDITOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V544000·2020-09-08
2021 Coachmen Catalina Recalled Due to Griddle Fire Risk
Forest River is recalling 2021 Coachmen Catalina trailers because a long griddle hose allows open flames to be stowed inside, increasing fire risk.
Product
COACHMEN — COACHMEN CATALINA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V542000·2020-09-04
Pleasure Way Tofino Motorhomes Recalled for Electrical Fire Risk
Pleasure Way is recalling 2019-2021 Tofino motorhomes because a damaged circuit board could increase the risk of a fire.
Product
PLEASURE WAY — PLEASURE WAY TOFINO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V543000·2020-09-04
Hyundai Tucson 2016-2021: Engine Compartment Fire from Brake Control Unit
Hyundai is recalling 2016-2021 Tucson vehicles because the Anti-lock Brake Hydraulic Electronic Control Unit could corrode and cause an electrical short, creating a risk of engine compartment fire.
Product
HYUNDAI — HYUNDAI TUCSON
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-09042020-01·2020-09-04
USDA Issues Public Health Alert for Ineligible Imported Cooked Duck Blood Curds
USDA FSIS issued a public health alert for imported cooked duck blood curds from China that lack required inspection certificates, making them unfit for human consumption.
Product
FSIS Issues Public Health Alert for Ineligible Imported Cooked Duck Blood Curds from China
Category
Food
Distribution
Distributed nationwide