State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55701–55725 of 74005

SevereFDA (Devices)·Z-0889-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender II Infusion Sets Due to Tubing Detachment
Roche Diagnostics is recalling ACCU-CHEK Tender II infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender II 13/60 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0896-2015·2015-01-07
Hansen Medical Recalls Sensei X Robotic Catheter Systems Due to Loose Clamp
Hansen Medical is recalling Sensei X Robotic Catheter Systems because a mechanical clamp may become loose, causing the device to fall and potentially injure patients or users.
Product
Sensei X Robotic Catheter System, model numbers 02057 and 08257. - Set up joint (SUJ)mechanical clamp that secures the SUJ to the catheter laboratory table. Product Usage: The Sensei X Robotic Catheter System is an electromechanical software controlled system designed to…
Category
Medical Device
Distribution
Distributed nationwide
SevereUSDA FSIS·002-2015·2015-01-07
Nijiya Market Recalls Frozen Boneless Beef Imported Without Inspection
Nijiya Market is recalling approximately 359 pounds of frozen boneless beef products produced in Japan that were not presented for USDA inspection at the U.S. point of entry.
Product
California Firm Recalls Boneless Beef Products Imported Without Benefit of Inspection
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·15V002000·2015-01-07
Polaris Recalls Victory Motorcycles Due to Fuel Pump Defect
Polaris is recalling certain Victory motorcycles because a manufacturing defect may cause the fuel pump to seize, leading to stalling and an increased risk of a crash.
Product
VICTORY — VICTORY HAMMER EIGHT BALL, CROSS ROADS, HIGH BALL, VEGAS EIGHT BALL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0893-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender II Infusion Sets Due to Tubing Detachment
Roche is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0899-2015·2015-01-07
Smiths Medical Recalls Hypodermic Needles Due to Safety Sheath Failure
Smiths Medical ASD, Inc. is recalling 10,000 units of Needle Pro Edge Safety Hypodermic Needles because the needle may not be captured in the safety sheath.
Product
Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 5mL Luer lock syringe; Reorder Number: 452010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0886-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk
Roche Diagnostics is recalling 13,041 boxes of ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender I 17/60 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections through…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0892-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender II Infusion Sets Due to Tubing Detachment
Roche is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender II 17/60 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0885-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk
Roche Diabetes Care is recalling ACCU-CHEK Tender I infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender I 13/110 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0884-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender I 13/80 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections through…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0891-2015·2015-01-07
ACCU-CHEK Tender II Infusion Sets Recalled for Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender II 13/110 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0890-2015·2015-01-07
ACCU-CHEK Tender II Infusion Sets Recalled for Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender II 13/80 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0887-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender I 17/80 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections through…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0883-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK¿ Tender I 13/60 10 pieces Product Usage: Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0876-2015·2015-01-07
Bard Caliber Inflation Device Recalled for Pressure Limitations
Perouse Medical is recalling Bard Caliber inflation devices that may fail to reach required pressure, potentially delaying angioplasty procedures.
Product
Bard Caliber (CL3030) Inflation Device Product Usage: Inflation Device intended for use during cardiovascular to create and maintain, monitor pressure in the balloon catheter - balloon inflation device for angioplasty procedures
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0898-2015·2015-01-07
Smiths Medical Recalls Hypodermic Needles Due to Safety Sheath Failure
Smiths Medical ASD, Inc. is recalling specific lots of Needle Pro Edge safety hypodermic needles because the needle is not captured in the safety sheath.
Product
Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 10mL Luer lock syringe; Reorder Number: 4102010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0895-2015·2015-01-07
Atricure CryoICE Cryogenic Probe Recalled for Potential Sterility Compromise
Atricure Inc is recalling 19,190 CryoICE cryogenic probes due to packaging defects that may have compromised sterility.
Product
Cryogenic probe for cardiac ablation surgery, packaged individually in Tyvek pouches Product Usage: Cryogenic probe for cardiac ablation surgery. The CryoICE cryoablation probe is a sterile, single use device intended to use in the cryosurgical treatment of cardiac…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0897-2015·2015-01-07
Smiths Medical Needle Pro Edge Safety Device Recall for Uncaptured Needles
Smiths Medical ASD, Inc. is recalling specific lots of Needle Pro Edge Safety Devices because the needle is not captured in the safety sheath.
Product
Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0894-2015·2015-01-07
ACCU-CHEK Tender II Infusion Sets Recalled for Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender II 17/110 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0888-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender I 17/110 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0877-2015·2015-01-07
Perouse Medical Recalls Synthes Inflation System Due to Pressure Limitations
Perouse Medical is recalling 2,184 units of the Synthes Inflation System because the device may fail to raise pressure above 10 atm, potentially delaying procedures.
Product
Synthes Inflation System (03.804.4135) Product Usage: Inflation system is used during kyphoplasty or other interventional kyphoplasty or other interventional procedures, to create and monitor pressure In the balloon catheter and pressure In the balloon catheter and to to…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V001000·2015-01-05
MCI Recalls J4500 Motor Coaches Due to Brake Hose Wear Risk
Motor Coach Industries is recalling 2013-2015 MCI J4500 motor coaches because a brake hose may rub against the tire or control arm, potentially causing a loss of braking power.
Product
MCI — MCI J4500
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0868-2015·2014-12-31
Halyard Health Recalls KimVent Microcuff Endotracheal Tubes Due to Detachment Risk
Halyard Health is recalling KimVent Microcuff Subglottic Suctioning Endotracheal Tubes because the cuff inflation line may detach during use.
Product
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 8.5 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0585-2015·2014-12-31
Heart Sync Defibrillation Electrodes Recalled for Incompatibility with Philips AEDs
Heart Sync, Inc. is recalling Adult Radiotranslucent Electrodes because they do not connect with Philips FR3 or FRx AED units, potentially preventing defibrillation.
Product
ADULT Radiotranslucent Electrode, Part number T100LO-PHILIPS, Rx ONLY, For use with Philips HeartStart AED "Comparable to Philips Medical HeartStart Electrodes Plug Style Connector", Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring, Single use.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0867-2015·2014-12-31
Halyard Health Recalls KimVent Microcuff Endotracheal Tubes Due to Detachment Risk
Halyard Health is recalling KimVent Microcuff Endotracheal Tubes because the cuff inflation line may detach during use, potentially compromising airway management.
Product
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 8.0 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.
Category
Medical Device
Distribution
Distributed nationwide