State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59076–59100 of 74011

HighFDA (Devices)·Z-1208-2014·2014-03-19
DePuy S-ROM Noiles Rotating Hinge Femur Recall for Sterile Barrier Defects
DePuy Orthopaedics is recalling S-ROM Noiles Rotating Hinge Femur devices due to potential holes in the sterile barrier pouches.
Product
REF 623421 RS-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Right , X-Small, Sterile R Qty 1 The S-ROM Hinged knee femoral component is used in revision surgeries when there is significant bone loss or ligament instability and additional support is…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1161-2014·2014-03-19
Smith & Nephew RENASYS-G Gauze Dressing Kit Recall for Sealing Issues
Smith & Nephew is recalling RENASYS-G Sterile Gauze Dressing Kits due to inadequate Soft Port sealing that may prevent fluid evacuation and fail to trigger alarms.
Product
Smith & Nephew RENASYS-G Sterile, Gauze Dressing Kit with Soft Port REF #'s: 66800961 (The RENASYS Soft Port Dressing Kits are used in conjunction with negative pressure wound therapy pumps)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1162-2014·2014-03-19
Smith & Nephew RENASYS-AB Abdominal Dressing Kit Recall for Sealing Defects
Smith & Nephew is recalling RENASYS-AB Abdominal Dressing Kits because inadequate sealing may prevent fluid evacuation and fail to trigger pump alarms.
Product
Smith & Nephew RENASYS-AB Abdominal Dressing Kit with Soft Port REF #'s: 66800980 (The RENASYS Soft Port Dressing Kits are used in conjunction with negative pressure wound therapy pumps)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1171-2014·2014-03-19
Biomet 3i Recalls Dental Torque Driver Kits Due to Sterility Failure
Biomet 3i is recalling 181 dental torque driver kits because they failed to meet required sterility assurance levels during validation testing.
Product
Contra-Angle Torque Driver Kit For Certain and External Connection Product Usage: Molded plastic tray used in holding various dental instruments for autoclave processing.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1157-2014·2014-03-19
Smith & Nephew RENASYS Soft Port Dressing Kits Recalled for Sealing Defects
Smith & Nephew is recalling RENASYS Soft Port Dressing Kits because inadequate sealing may prevent wound fluid evacuation and fail to trigger pump alarms.
Product
Smith & Nephew RENASYS Soft Port REF: 66800799 (The RENASYS Soft Port Dressing Kits are used in conjunction with negative pressure wound therapy pumps)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1173-2014·2014-03-19
Horiba Medical Recalls ABX PENTRA ML Software Due to Data Transmission Bug
Horiba Medical is recalling ABX PENTRA ML software because a bug may transmit incorrect results to Laboratory Information Systems.
Product
Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s): N/A Software Version(s): All versions are subject to this correction. Product Usage: The ABX PENTRA ML is a software data management system intended for use on ABX Hematology Analyzers.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1160-2014·2014-03-19
Smith & Nephew Recalls RENASYS Gauze with Soft Port Kits
Smith & Nephew is recalling RENASYS Gauze with Soft Port Kits because inadequate sealing can cause fluid to remain under the dressing and prevent the pump alarm from activating.
Product
Smith & Nephew RENASYS-Gauze with Soft Port Kit REF #'s: 66800933, 66800934, 66800935, and 66800936 (The RENASYS Soft Port Dressing Kits are used in conjunction with negative pressure wound therapy pumps)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1205-2014·2014-03-19
DePuy S-ROM Noiles Rotating Hinge Femur Recall for Sterile Barrier Defect
DePuy Orthopaedics is recalling S-ROM Noiles Rotating Hinge Femur devices because holes may develop in the sterile barrier pouches, potentially compromising sterility.
Product
REF 623411 L, S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Left, Small, Sterile R Qty 1 The S-ROM Hinged knee femoral component is used in revision surgeries when there is significant bone loss or ligament instability and additional support is…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1194-2014·2014-03-19
Philips HeartStart MRx Monitor/Defibrillator Recalled for Q-CPR Meter Display Error
Philips is recalling HeartStart MRx Monitor/Defibrillators with the Q-CPR Meter option because the device may incorrectly display a 'Do Not Touch the Patient' icon during defibrillation mode.
Product
Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with Q-CPR Meter Option B08 The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1204-2014·2014-03-19
DePuy S-ROM Noiles Rotating Hinge Femur Recalled for Sterile Barrier Defects
DePuy Orthopaedics is recalling S-ROM Noiles Rotating Hinge Femur devices because holes may develop in the sterile barrier pouches, potentially compromising sterility.
Product
REF 623401 R, S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Right, Medium, Sterile R Qty 1 The S-ROM Hinged knee femoral component is used in revision surgeries when there is significant bone loss or ligament instability and additional support is…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1174-2014·2014-03-19
Synthes Small Notch Titanium Reconstructive Plate Recalled for Contraindicated Spine Use
Synthes, Inc. is recalling Small Notch Titanium Reconstructive Plate sets distributed for spine applications where they are contraindicated.
Product
Synthes Small Notch Titanium Reconstructive Plate Product Usage: The Synthes Small Notch Titanium Reconstructive Plate set offers fixation for immediate stabilization to allow bone fusion. Commercially pure titanium implants are biocompatible. The wide selection of implants…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1175-2014·2014-03-19
GE Healthcare Recalls CARESCAPE Patient Monitors Due to Safety Issues
GE Healthcare is recalling CARESCAPE Monitor B650 and B850 units due to potential safety issues with Non-Invasive Blood Pressure and Bed to Bed functions.
Product
GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239 CARESCAPE Monitor B650 The CARESCAPE Monitor B650 is a multi-parameter patient monitor intended for use in multiple areas and intra-hospital transport within a professional healthcare facility. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1207-2014·2014-03-19
DePuy S-ROM Noiles Rotating Hinge Femur Recall for Sterile Barrier Defect
DePuy Orthopaedics is recalling S-ROM Noiles Rotating Hinge Femur devices because holes may develop in the sterile barrier pouches, potentially compromising sterility.
Product
REF 623421 L S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Left , X-Small, Sterile R Qty 1 The S-ROM Hinged knee femoral component is used in revision surgeries when there is significant bone loss or ligament instability and additional support is…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1200-2014·2014-03-19
GE Healthcare Recalls Elscint APEX Helix Gamma Cameras for Motion Risk
GE Healthcare is recalling 3,062 Elscint APEX Helix gamma cameras due to a potential safety issue where the detector may drift toward the patient.
Product
Elscint APEX Helix, dual-head, multi-purpose, Slip-Ring, digital gamma camera Product Usage: The intended use of the Quasar system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using a variety of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1158-2014·2014-03-19
Smith & Nephew RENASYS-F Foam Dressing Kit Recall for Sealing Issues
Smith & Nephew is recalling RENASYS-F Foam Dressing Kits with Soft Port due to inadequate sealing that may prevent fluid evacuation and fail to trigger alarms.
Product
Smith & Nephew RENASYS-F Foam Dressing Kit with Soft Port REF #'s: 66800794, 66800795, and 66800796 (The RENASYS Soft Port Dressing Kits are used in conjunction with negative pressure wound therapy pumps)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1172-2014·2014-03-19
Accumetrics Recalls VerifyNow IIb/IIIa Test Kits Due to Erroneous Results
Accumetrics is recalling VerifyNow IIb/IIIa test kits because they may report erroneous low platelet aggregation unit results, potentially affecting clinical decisions.
Product
VerifyNow IIb/IIIa Test, Catalog No. 85310, 10-Test Kit and Catalog No. 85011, 25-Test kit. Product Usage: The VerifyNow System is a turbidimetric based optical detection system which measures platelet-induced aggregation. The system consists of an instrument, a disposable…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1155-2014·2014-03-19
Philips HeartStart MRx Monitor/Defibrillator Recalled for Shock Delivery Failure
Philips is recalling HeartStart MRx Monitor/Defibrillators because they may display a Red X during automated tests, indicating a failure that could prevent the delivery of a shock or pacing.
Product
Philips HeartStart MRx Monitor/Defibrillator Model numbers: M3535A, M3536A, M3536M,M3536M4,M3536M6,861288,861289,861464,861483,and 861491
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V135000·2014-03-19
McNeilus Concrete Mixers Recalled for Falling Extension Chutes
McNeilus is recalling 2013-2014 Concrete Standard and Bridgemaster V mixers because extension chutes may fall from the rack, creating a road hazard.
Product
MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER, STANDARD MIXER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1198-2014·2014-03-19
GE Healthcare Recalls Infinia Nuclear Medicine Systems for Detector Motion Risk
GE Healthcare is recalling Infinia and Infinia Hawkeye Nuclear Medicine Systems due to a potential safety issue where the detector may drift toward the patient.
Product
GE Healthcare Infinia and Infinia Hawkeye Nuclear Medicine Systems. For Dual-Head Variable Angle Gamma Camera, Hawkeye Option for Dual-Head Variable Angle Gamma Camera (this includes GE Quasar Nuclear Medicine Systems). Nuclear Medicine Systems Infinia devices Product Usage…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1170-2014·2014-03-19
Biomet 3i Recalls Dental Torque Driver Kits Due to Sterility Failure
Biomet 3i is recalling 250 Contra-Angle Torque Driver Kits because the included surgical trays failed to meet required Sterility Assurance Levels during validation testing.
Product
Contra-Angle Torque Driver Kit For Certain Internal Connection Product Usage: Molded plastic tray used in holding various dental instruments for autoclave processing.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14132·2014-03-19
Vera Bradley Recalls Bear Rattles and Bunny Toys for Choking Hazard
Vera Bradley is recalling about 98,000 Bear Ring Rattles and Bunny stuffed toys because the pom-pom tail can detach, posing a choking hazard to young children.
Product
Vera Bradley Bear Ring Rattles and Bunny Stuffed Toys
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1206-2014·2014-03-19
DePuy S-ROM Rotating Hinge Femoral Components Recalled for Sterile Barrier Defects
DePuy Orthopaedics is recalling S-ROM Noiles Rotating Hinge Femoral components due to potential holes in the sterile barrier pouches.
Product
REF 623411 R S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Right, Small, Sterile R Qty 1 The S-ROM Hinged knee femoral component is used in revision surgeries when there is significant bone loss or ligament instability and additional support is…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1153-2014·2014-03-19
Actavis Recalls Alprazolam 1 mg Tablets Due to Significant Tablet Erosion
Actavis Elizabeth LLC is recalling 9,447 bottles of Alprazolam 1 mg tablets because complaints reported significant tablet erosion.
Product
ALPRAZOLAM — ALPRAZOLAM (ALPRAZOLAM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1195-2014·2014-03-19
Veridex Recalls CELLTRACKS Analyzer II Microscopes Due to Camera Failures
Veridex, LLC is recalling 19 CELLTRACKS Analyzer II fluorescence microscopes because of reported camera failures. The devices are used for analyzing rare cells in biological fluids.
Product
CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS ANALYZER II¿ is a semi-automated fluorescence microscope, consisting of the analyzer, a dedicated computer with CELLTRACKS¿ software, monitor, keyboard, mouse and uninterruptible power supply (UPS).…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1154-2014·2014-03-19
Clarity Medical Systems Recalls RetCam Devices Due to Age Calculation Error
Clarity Medical Systems is recalling RetCam 3, Portable, and Shuttle devices because a software error causes incorrect patient age calculations.
Product
RetCam 3, RetCam Portable and RetCam Shuttle; manufactured by Clarity Medical Systems, Inc.; Pleasanton, CA 94588. General ophthalmic imaging including retinal, corneal and external imaging.
Category
Medical Device
Distribution
Distributed nationwide