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.

39126–39150 of 73919

SevereFDA (Devices)·Z-1127-2018·2018-03-28
MedComp Repair Kit Recalled for Potential Connection Failures and Blood Loss Risk
Medical Components, Inc. is recalling 1,575 MedComp Repair Kits due to potential connection failures that could lead to blood loss or air emboli.
Product
REPAIR KIT, REF RPK-01, UDI 884908039856 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1124-2018·2018-03-28
MedComp Recalls 12F Tesio Catheter Sets Due to Connection Failure Risk
Medical Components, Inc. is recalling 12F Tesio Catheter Sets because connection failures may cause blood loss or air emboli.
Product
12F Tesio CATHETER SET (CUFF 32CM FROM TIP), REF MCTC1247SD, UDI 884908027266 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1118-2018·2018-03-28
MedComp Recalls Catheter Repair Kits Due to Connection Failure Risk
Medical Components, Inc. is recalling 93 Catheter Repair Kits because potential connection failures could lead to blood loss or air emboli.
Product
CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18V201000·2018-03-28
LGS Recalls 2018 Pace, Look, and Cargo Express Cargo Trailers
LGS Industries is recalling 2018 Pace, Look, and Cargo Express cargo trailers because a spindle weld on the axle may fail, potentially causing loss of vehicle control.
Product
LOOK — LOOK, PACE, CARGO EXPRESS CARGO TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1100-2018·2018-03-28
Boston Scientific Recalls Malecot Nephrostomy Catheters Due to Breakage
Boston Scientific is recalling Malecot Nephrostomy Catheter Sets because they may break at the mid-shaft bond during use.
Product
Malecot Nephrostomy Catheter Set, Product Number: M0064101000, GTIN: 08714729005261 The Malecot Nephrostomy Catheter Set is intended to establish percutaneous nephrostomy drainage and is indicated for the following: Diagnostic Indications: " Antegrade pyelography "…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1125-2018·2018-03-28
MedComp Two Part Adapter Recall for Potential Connection Failures
Medical Components, Inc. is recalling 35 MedComp Two Part Adapter kits due to potential connection failures that could cause blood loss or air emboli.
Product
TWO PART ADAPTER, REF MCTLA2000, UDI 884908027310 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1133-2018·2018-03-28
Boston Scientific Recalls SpyScope DS Biliary Catheters Due to Sleeve Defect
Boston Scientific is recalling 5,026 units of SpyScope DS Access and Delivery diagnostic biliary catheters because a sleeve may protrude, causing tissue damage or bleeding.
Product
SpyScope DS Access and Delivery diagnostic biliary catheter, M00546600
Category
Medical Device
Distribution
Distributed nationwide
SevereUSDA FSIS·026-2018·2018-03-28
Tony Downs Recalls Chicken Products Due to Possible Plastic Contamination
Tony Downs Foods is recalling approximately 96,384 pounds of canned chicken breast products that may contain hard plastic. The recall was initiated after two consumer complaints regarding foreign matter.
Product
Tony Downs Foods — Tony Downs Food Company, Inc. Recalls Chicken Products due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
SevereCPSC·18732·2018-03-28
Shop LC Recalls Electric Blankets Due to Fire and Burn Hazards
Shop LC is recalling electric heated throw blankets because the heating coils can overheat, posing fire and burn hazards.
Product
Electric heated micro plush flannel sherpa throw blankets
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0194-2018·2018-03-28
Monteris Medical Recalls NeuroBlate Systems Due to MRI Interaction
Monteris Medical Corp is recalling 52 NeuroBlate systems used for MRI-guided neurosurgery due to an unanticipated interaction with 1.5 Tesla MRI systems.
Product
MONTERIS MEDICAL NEUROBLATE SYSTEM, used for MRI-guided neurosurgical ablation.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1123-2018·2018-03-28
MedComp Recalls 12F Modified Tesio Catheter Sets Due to Connection Failures
Medical Components, Inc. is recalling 40 kits of 12F Modified Tesio Catheter Sets because connection failures could cause blood loss or air emboli.
Product
12F MODIFIED Tesio CATHETER SET, REF MCTC1235SM, UDI 884908027259 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1119-2018·2018-03-28
MedComp Repair Kit Recalled for Potential Connection Failures
Medical Components, Inc. is recalling 5 MedComp Repair Kits due to potential connection failures that could cause blood loss or air emboli.
Product
REPAIR KIT, REF ARA101, UDI 884908083637 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1104-2018·2018-03-28
Boston Scientific Recalls Malecot Nephrostomy Catheters Due to Mid-Shaft Breakage
Boston Scientific is recalling certain Malecot Nephrostomy Catheters because they are breaking at the mid-shaft bond during use.
Product
Percutaneous Access Set, Product Number: M0064201150, GTIN: 08714729009757 The Malecot Nephrostomy Catheter Set is intended to establish percutaneous nephrostomy drainage and is indicated for the following: Diagnostic Indications: " Antegrade pyelography " Pressure/perfusion…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18V200000·2018-03-28
Toyota Recalls 2018 Camry Vehicles Due to Engine Piston Defect
Toyota is recalling 2018 Camry vehicles with 2.5L engines because oversized pistons may cause the engine to stall, increasing crash risk.
Product
TOYOTA — TOYOTA CAMRY
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1132-2018·2018-03-28
NxStage PureFlow B Solution Recalled for Missing Labeling Warnings
NxStage Medical is recalling 1,243,400 units of PureFlow B Solution because the original labeling failed to warn against mixing dialysate formulations.
Product
NxStage PureFlow B Solution - Premixed Dialysate for Hemodialysis with NxStage System One
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1135-2018·2018-03-28
Smiths Medical Medfusion Syringe Pumps Recalled for Syringe Misidentification
Smiths Medical is recalling Medfusion Syringe Pumps because they may fail to recognize or misidentify loaded medication syringes, preventing proper programming.
Product
Medfusion Syringe Pump 3500 Series The Medfusion¿ Syringe Infusion Pumps are indicated for the following uses: 1) Administration of fluids requiring precisely controlled infusion rates including blood or blood products, lipids, drugs, antibiotics, enteral solutions and other…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1103-2018·2018-03-28
Boston Scientific Recalls Re-Entry Malecot Nephrostomy Catheter Sets
Boston Scientific is recalling specific Re-Entry Malecot Nephrostomy Catheter Sets because they may break at the mid-shaft bond during use.
Product
Re-Entry" Malecot Nephrostomy Catheter Set, Product Number: M0064101050, GTIN: 08714729192268 The Malecot Nephrostomy Catheter Set is intended to establish percutaneous nephrostomy drainage and is indicated for the following: Diagnostic Indications: " Antegrade pyelography "…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1134-2018·2018-03-28
Medfusion Syringe Pumps Recalled for Syringe Misidentification Risk
Smiths Medical ASD Inc. is recalling Medfusion Syringe Pumps because they may fail to recognize or misidentify loaded medication syringes, potentially preventing proper pump programming.
Product
Medfusion Syringe Pump 4000 Series The Medfusion¿ Syringe Infusion Pumps are indicated for the following uses: 1) Administration of fluids requiring precisely controlled infusion rates including blood or blood products, lipids, drugs, antibiotics, enteral solutions and other…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1099-2018·2018-03-28
Boston Scientific Recalls Malecot Nephrostomy Catheters Due to Breakage
Boston Scientific is recalling 422 units of Malecot Nephrostomy Catheters because they may break at the mid-shaft bond during use.
Product
Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Malecot and the Stenting Malecot Catheters are designed for percutaneous drainage within the renal collecting system while maintaining external access. The Stenting Malecot Nephrostomy…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1101-2018·2018-03-28
Boston Scientific Recalls Malecot Nephrostomy Catheters Due to Mid-Shaft Breakage
Boston Scientific is recalling Malecot Nephrostomy Catheter Sets because they are breaking at the mid-shaft bond during use.
Product
Malecot Nephrostomy Catheter Set, Product Number: M0064101010, GTIN: 08714729005278 The Malecot Nephrostomy Catheter Set is intended to establish percutaneous nephrostomy drainage and is indicated for the following: Diagnostic Indications: " Antegrade pyelography "…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V202000·2018-03-28
REV Recalls Motorhomes Due to Potential Satellite Dish Detachment
REV is recalling 2017-2018 motorhomes because satellite dish mounting screws may not be fastened correctly, posing a crash risk if the dish detaches.
Product
HOLIDAY RAMBLER — HOLIDAY RAMBLER, AMERICAN COACH, FLEETWOOD PRODIGY, AMERICAN EAGLE, NAVIGATOR, PULSE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1121-2018·2018-03-28
MedComp Recalls Tesio Catheter Sets Due to Connection Failure Risk
Medical Components, Inc. is recalling 55 Tesio Catheter Sets because potential connection failures could lead to blood loss or air emboli.
Product
12F X 60CM TESIO CATHETER SET WITH "Y" ADAPTOR, REF CMD757, UDI 884908005554 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1136-2018·2018-03-28
Smiths Medical Recalls Medfusion Syringe Pumps Due to Syringe Recognition Issues
Smiths Medical is recalling Medfusion Syringe Pumps because they may fail to recognize or misidentify loaded medication syringes, potentially preventing proper pump programming.
Product
Medfusion Syringe Pump 3010 Series The Medfusion¿ Syringe Infusion Pumps are indicated for the following uses: 1) Administration of fluids requiring precisely controlled infusion rates including blood or blood products, lipids, drugs, antibiotics, enteral solutions and other…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1126-2018·2018-03-28
MedComp Catheter Repair Kit Recalled for Potential Connection Failures
Medical Components, Inc. is recalling 315 Catheter Repair Kits due to potential connection failures that could cause blood loss or air emboli.
Product
CATHETER REPAIR KIT, REF RMS52001, UDI 884908039658 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1120-2018·2018-03-28
MedComp Recalls Tesio Catheter Sets Due to Connection Failure Risk
Medical Components, Inc. is recalling 712 Tesio catheter sets because connection failures could cause blood loss or air emboli.
Product
12F X 40CM TESIO CATHETER SET WITH "Y" ADAPTOR, REF CMD755, UDI 884908005530 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide