State

US Virgin Islands product recalls

73,104 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 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12001–12025 of 73281

HighFDA (Devices)·Z-1341-2024·2024-03-27
Angiodynamics Guidewire Introducer Recall Due to Manufacturing Defect
Angiodynamics recalls approximately 5,840 guidewire introducers with manufacturing defects that may prevent proper guidewire insertion during vascular procedures. The defect could cause procedural delays requiring equipment exchange.
Product
MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-759
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1343-2024·2024-03-27
Vascular Guidewire Introducer Sheath Recalled for Internal Hub Defect
Angiodynamics recalls 130 MINI STICK MAX guidewire introducers due to hub voids that may prevent guidewire passage during vascular procedures. No injuries reported.
Product
MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-765
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1304-2024·2024-03-27
Siemens DCA HbA1c Reagent Kit Recalled for Inaccurate Test Results
Siemens is recalling its DCA HbA1c Reagent Kit because the device displays falsely elevated readings without alerting the user. This could lead to incorrect patient management of glucose levels.
Product
DCA Systems HbA1c Reagent Kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1309-2024·2024-03-27
Nautilus ECMO Oxygenator recalled due to heat exchanger water path restriction
Mc3 Inc recalls Nautilus ECMO Oxygenator units due to heat exchanger water path restriction that degrades temperature control performance. Inadequate heat transfer may lead to hypothermia risk.
Product
NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: (1) 48145; (2) 48145E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1319-2024·2024-03-27
I.B.S. 6.5-C Compression Screw Batch Recalled for Dimensional Mix-Up
A batch of I.B.S compression screws may have incorrect dimensions compared to their labels due to a batch mix-up. The 59 affected units were distributed nationwide in Tennessee.
Product
I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 75mm,Part Number S65 ST175
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1322-2024·2024-03-27
Dental Implant Impression Coping Recalled for Manufacturing Defect
Thommen Medical AG is recalling impression coping units because the internal canal depth was not manufactured according to specifications, preventing firm connection to the dental implant. The product was distributed in Ohio and Kentucky.
Product
impression coping, repositionable, short, screw-retained, PF 4.0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1307-2024·2024-03-27
Nasal Intubation Kit Recalled for Incompatible Tube Holder
Curaplex Nasal Intubation Kit recalled because the included endotracheal tube holder is incompatible with nasal intubation procedures, preventing practitioners from properly securing the tube.
Product
Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023060S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1340-2024·2024-03-27
Vascular Guidewire Introducer Recalled Due to Internal Hub Defect
A vascular guidewire introducer is recalled because internal voids in the hub may prevent proper guidewire passage, potentially delaying surgical procedures.
Product
MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-758
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1317-2024·2024-03-27
Medtronic Abre Venous Stent System Recalled for Sterile Package Breach
Medtronic is recalling Abre Venous Self-expanding Stent Systems due to a potential for sterile package breach. The recalled systems consist of three product numbers totaling 65 units distributed worldwide. No injuries have been reported.
Product
Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1337-2024·2024-03-27
Guidewire Introducer Recalled for Manufacturing Defect Affecting Device Function
Angiodynamics is recalling 58 units of its MINI STICK MAX guidewire introducer due to voids in the internal lumen that may prevent proper guidewire passage. Users may experience procedural delay requiring device exchange.
Product
MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-752
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1349-2024·2024-03-27
Landauer microStar Reader dosimetry system discontinued for medical applications
Landauer is permanently discontinuing the microStar Reader medical dosimetry system. The company is removing product documentation references and discontinuing use with medical dosimeters.
Product
microStar Reader, Model Numbers: 10015-000 (marketed in EMEA as 100, 102, 110, and 201), 10016-000 (marketed in EMEA as 101), 10036-000, 10044-000, 10055-000, BC30058, and BC30059
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1336-2024·2024-03-27
FDA Recalls Vascular Guidewire Introducer Due to Manufacturing Defect
Angiodynamics is recalling 959 units of MINI STICK MAX guidewire introducers due to voids in the sheath hub that may prevent proper guidewire placement. Users may experience procedure delays and need to exchange equipment.
Product
MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-751
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1338-2024·2024-03-27
Vascular Guidewire Introducer Sheath Recall Due to Manufacturing Defect
Angiodynamics is recalling certain MINI STICK MAX vascular guidewire introducer sheaths due to internal voids that may prevent guidewire passage during surgery, potentially causing procedural delays.
Product
MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 2.75" PG -Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-754
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1335-2024·2024-03-27
Angiodynamics Guidewire Introducer Devices Recalled for Manufacturing Defects
Angiodynamics recalls MINI STICK MAX guidewire introducer devices due to manufacturing defects in the internal lumen that may prevent guidewire passage and delay surgical procedures.
Product
MINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-750
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1346-2024·2024-03-27
Guidewire Introducer Sheath from Angiodynamics Recalled for Manufacturing Defect
Angiodynamics is recalling 65 units of its MINI STICK MAX guidewire introducer sheath due to manufacturing defects that may prevent guidewires from passing through during surgical procedures.
Product
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-775
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1313-2024·2024-03-27
Steris Endo Cleaning Indicator Recalled Due to Temperature Excursion
Mckesson Medical-Surgical is recalling Steris Endo Cleaning Indicator VERIFY RESITEST devices due to temperature excursions that occurred on January 8, 2024. The temperature drop could cause the indicator to produce incorrect or delayed test results.
Product
Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1311-2024·2024-03-27
Sekisui OSOM BVBLUE Bacterial Vaginosis Control Kit recalled due to temperature exposure
A Sekisui Diagnostics control kit for bacterial vaginosis testing was recalled after exposure to temperatures below the validated storage range for up to 60 minutes due to refrigerator mechanical failure.
Product
Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1315-2024·2024-03-27
Laboratory Control Material Recalled Due to Temperature Storage Excursion
Abbott Point of Care Control i-STAT Level 3 control material (Lot 121164) is being recalled due to temperature excursions in storage that could affect test accuracy. Affected units were distributed in Arizona, Pennsylvania, and Texas.
Product
Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1339-2024·2024-03-27
Angiodynamics surgical guidewire recalled for manufacturing defect
Angiodynamics is recalling 5,176 units of MINI STICK MAX guidewires due to manufacturing voids that prevent passage through the introducer during surgery. Surgeons may need to exchange the sheath to complete procedures.
Product
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1305-2024·2024-03-27
Conductive Adhesive Gel Recalled Due to Thickness and Discoloration Issues
Natus Neurology is recalling TENSIVE Conductive Adhesive Gel (Lot A0623009) after complaints of improper thickness, discoloration, and in one case, patient skin irritation following use.
Product
TENSIVE Conductive Adhesive Gel, REF 016-401600
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1306-2024·2024-03-27
Natus Sleep Supplies Recalled for Conductive Adhesive Gel Quality Defects
Natus Neurology is recalling Sleep Supplies Start Kits due to defective conductive adhesive gel supplied by Parker Laboratories. The gel is too thick, discolored, and caused patient irritation in at least one case.
Product
natus neurology, Sleep Supplies Start Kit with Single Use Supplies for Embla EX Series Amplifiers, REF 024252
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1344-2024·2024-03-27
Guidewire Introducer Sheath with Manufacturing Defect Recalled by Angiodynamics
Angiodynamics is recalling MINI STICK MAX guidewire introducer sheaths due to manufacturing defects that may prevent guidewire passage. The defect may cause procedural delays requiring equipment exchange during vascular interventions.
Product
MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-767
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V230000·2024-03-25
Doosan Portable Generator Trailers Recalled for Brake Wiring Defect
Doosan is recalling 2015-2023 Portable Generator Trailers because the electric brake harness was incorrectly wired, potentially disabling brakes.
Product
DOOSAN PORTABLE POWER — DOOSAN PORTABLE POWER MOBILE GENERATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V225000·2024-03-24
Mercedes-Benz Recalls 2023 Sprinter Vans for Electrical Fire Risk
Daimler Vans USA is recalling 2023 Mercedes-Benz Sprinter vans because a 12-volt ground connection may overheat, increasing the risk of fire or loss of drive power.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 3500, SPRINTER 2500, SPRINTER 4500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V226000·2024-03-22
Ford Recalls 2023-2024 Transit Vehicles for Tire Contact Defect
Ford is recalling 2023-2024 Transit vehicles with the Trail package because tires may contact the wheel arch liner, risking tire damage and loss of control.
Product
FORD — FORD TRANSIT
Category
Vehicle
Distribution
Distributed nationwide