State

US Virgin Islands product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28776–28800 of 73774

HighFDA (Devices)·Z-2153-2020·2020-06-03
Biomet Vanguard Knee System Recalled for Elevated Endotoxin Levels
Biomet is recalling 93 Vanguard Knee System tibial bearings due to potential endotoxin levels exceeding specifications. The recall covers units distributed worldwide.
Product
Knee Products: 183742 Vanguard Knee System, PS+ Tibial Bearing, 12 MM, 71/75 MM EP-183608 Vanguard Knee System, PS Tibial Bearing, E1 Infused, 18 MM X 59 MM EP-183608 Vanguard Knee System, PS Tibial Bearing, E1 Infused, 18 MM X 59 MM 183744 Vanguard Knee…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2137-2020·2020-06-03
Philips HeartStart XL Monitor/Defibrillators Recalled for Missing Field Action Corrections
Philips is recalling 130 HeartStart XL Monitor/Defibrillators because they may not have received required corrections from prior field actions.
Product
Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product Usage: is for use in the hospital by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac life support, or defibrillation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2145-2020·2020-06-03
Biomet Recalls RingLoc Hip System Components Due to Endotoxin Levels
Biomet, Inc. is recalling specific RingLoc Hip System components due to potential elevated endotoxin levels that exceed specification limits.
Product
Hip Products Item Number: 1) 110010462 RingLoc Hip System, Acetabular Bi-Polar Cup, 28 MM X 51 MM 2) 11-165218 RingLoc Bi-Polar Hip System, Acetabular Cup, 28 MM X 47 MM 3) XL-105916 588500 RingLoc Hip System, Acetabular Liner, 36 MM, Size 26 Product Usage: Hemi hip…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2143-2020·2020-06-03
Spectranetics Bridge Occlusion Balloon Recalled for Thrombus Formation Risk
Spectranetics is recalling Bridge Occlusion Balloons because current labeling is insufficient to warn users about the risk of thrombus formation if the device remains in the vasculature for long durations.
Product
Bridge Occlusion Balloon, REF 590-001, QTY 1, Sheath Compatibility 12F, Guidewire Compatibility 0.035 in, Working Length 90 cm, Balloon Outer Diameter 31 mm, Balloon Length 80 mmm, Rx ONLY, CE Marking, Sterile EO, UDI: 00813132024666
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2154-2020·2020-06-03
Biomet Recalls Vanguard Knee Implants Due to Endotoxin Levels
Biomet, Inc. is recalling 91 Vanguard Knee System patella implants because they may contain elevated endotoxin levels that exceed specification limits.
Product
Knee Products: 184762 Knees Vanguard Knee System, Series-A Standard Patella, 28 MM; 184764 Knees Vanguard Knee System, Series-A Standard Patella, 31 MM Product Usage: Knee prosthesis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2136-2020·2020-06-03
Beckman Coulter Recalls ISE Electrolyte Reference Reagent Due to Calibration Failures
Beckman Coulter is recalling ISE Electrolyte Reference Reagent because low pH levels may cause calibration failures and false high patient results, potentially delaying treatment.
Product
ISE Electrolyte Reference (2 X 2L) Reagent, REF A28937, UDI: 15099590202491 - Product Usage: are intended for the quantitative determination of carbon dioxide in human serum or plasma.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2139-2020·2020-06-03
Radiometer ABL90 FLEX Analyzers Recalled for Hemolyzer Measurement Errors
Radiometer Medical ApS is recalling ABL90 FLEX analyzers and spare hemolyzer units because defective cuvettes cause light shunts, leading to inaccurate measurement results.
Product
ABL90 FLEX, model no. 393-090; and Spare Part Hemolyzer Units (902-980): R0526 - R0941 - Product Usage: are intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point-of-care setting.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2127-2020·2020-06-03
Siemens Cios Alpha X-Ray System Recalled for Electrical Shock Risk
Siemens is recalling 58 Cios Alpha X-Ray systems because unplugging the monitor cable can expose users to unsafe electrical voltage, posing a shock hazard.
Product
Cios Alpha Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA20-10308191 and VA30-10308194 The Cios Alpha and Cios Spin are a mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2148-2020·2020-06-03
Biomet Oxford Partial Knee Systems Recalled for Elevated Endotoxin Levels
Biomet, Inc. is recalling 76 units of Oxford Partial Knee Systems due to potential endotoxin levels exceeding specification limits.
Product
Knee Products: 154335 Oxford Partial Knee System, Fixed Lateral Tibial Construct, Left, Cemented, D3 154336 Oxford Partial Knee System, Fixed Lateral Tibial Construct, Left, Cemented, D4 154339 Oxford Partial Knee System, Fixed Lateral Tibial Construct, Left, Cemented, D7…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2138-2020·2020-06-03
Radiometer ABL90 FLEX Plus Analyzers Recalled for Measurement Errors
Radiometer Medical ApS is recalling ABL90 FLEX Plus analyzers and hemolyzer units because defective cuvettes cause inaccurate blood measurements.
Product
ABL90 FLEX PLUS, model no. 393-02; and Spare Part Hemolyzer Units (902-980): R0526 - R0941 - Product Usage: are intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point-of-care…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2132-2020·2020-06-03
Smith & Nephew Recalls Journey II Uni Resection Prep Trial Instruments
Smith & Nephew is recalling 200 units of Journey II Uni Resection Prep Trial instruments because a manufacturing defect could cause the device to disassemble during surgery.
Product
JOURNEY II UNI RESECTION PREP TRIAL, LEFT MEDIAL/ RIGHT LATERAL - Product Usage: The JOURNEY II Uni Resection Prep Trial is a reusable surgical instrument used during range of motion trialing to assess joint tension and component alignment during surgery. The provisional…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2147-2020·2020-06-03
Biomet Recalls Knee Prosthesis Components Due to Endotoxin Concerns
Biomet, Inc. is recalling 12 units of the Orthopedic Salvage System Tibial Bearing because of potential elevated endotoxin levels.
Product
Knee Products: 150414 Orthopedic Salvage System (OSS) Tibial Bearing, 20 MM Standard - Product Usage: Knee prosthesis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2133-2020·2020-06-03
Smith & Nephew Recalls Journey II Uni Resection Prep Trial Instruments
Smith & Nephew is recalling 195 reusable surgical instruments because a manufacturing defect could cause the device to disassemble during use.
Product
JOURNEY II UNI RESECTION PREP TRIAL, RIGHT MEDIAL/ LEFT LATERAL - Product Usage: The JOURNEY II Uni Resection Prep Trial is a reusable surgical instrument used during range of motion trialing to assess joint tension and component alignment during surgery. The provisional…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2135-2020·2020-06-03
MOTek Medical Recalls Body Weight Support Light Due to Yoke Detachment Risk
MOTek Medical is recalling 80 units of the Body Weight Support Light (Model RB011) because a manufacturing deviation may cause the yoke to detach from the cable guide.
Product
Body Weight Support (BWS) Light; Model No. RB011; a component of C-Mill, Grail, M-Gait - Product Usage: is designed to facilitate functional gait training of subjects with gait and/or balance impairment by providing dynamic partial vertical unloading during walking on a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2149-2020·2020-06-03
Biomet Recalls AGC Knee System Tibial Components Due to Endotoxin Levels
Biomet, Inc. is recalling 54 units of AGC Knee System PS Molded Tibial Components because they may contain elevated endotoxin levels that exceed specification limits.
Product
Knee Products: 155308 Knees AGC Knee System PS Molded Tibial Component, 10 MM X 65 MM 155326 Knees AGC Knee System PS Molded Tibial Component, 10 MM X 70 MM 155330 Knees AGC Knee System PS Molded Tibial Component, 14 MM X 70 MM 155344 Knees AGC Knee System PS Molded Tibial…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2144-2020·2020-06-03
Biomet Recalls Shoulder Implant Components Due to Endotoxin Levels
Biomet is recalling 122 units of specific shoulder implant components due to potential endotoxin levels exceeding specifications.
Product
Extremities Item Number: 1)113954 Hybrid Glenoid Glenoid Base, 4 MM 2) XL-115366 Comprehensive Reverse Shoulder Humeral Bearing, ArComXL, 44 MM X 41 MM, Standard 3) XL-115364 Comprehensive Reverse Shoulder Humeral Bearing, ArComXL, 44 MM X 36 MM, +3MM Standard Product…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2152-2020·2020-06-03
Biomet Recalls Vanguard Knee System Bearings Due to Endotoxin Levels
Biomet, Inc. is recalling 107 units of Vanguard Knee System PS Mono Lock Tibial Bearings because they may contain elevated endotoxin levels that exceed specification limits.
Product
Knee Products: 189420 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM 189422 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 63 MM 189442 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12 MM X 67 MM 189460 Vanguard Knee System, PS Mono Lock…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2156-2020·2020-06-03
Biomet Recalls Custom Knee Prosthesis Due to Potential Endotoxin Levels
Biomet, Inc. is recalling a specific custom-made knee prosthesis due to the potential presence of elevated endotoxin levels that exceed specification limits.
Product
Knee Products: TMJPM-1510 Microfixation Custom Made Device, Left PM-TMJ Model (01)00841036226534(17)220111(10)735550 Product Usage: Knee prosthesis
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V322000·2020-06-03
Mercedes-Benz and Freightliner Sprinter Vans Recalled for Seat Wiring Defect
Daimler Vans USA is recalling 2019-2020 Sprinter vans with swivel seats because incorrectly routed wiring may damage the front seat air bags.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER (VS30)
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2117-2020·2020-06-03
Abbott Recalls Architect iGentamicin Reagent Kits Due to Assay Interaction
Abbott is recalling 6,087 Architect iGentamicin Reagent Kits because they may interact with troponin assays, potentially impacting patient results.
Product
ARCHITECT iGentamicin Reagent Kit - Product Usage: The measurements obtained are used in the diagnosis and treatment of gentamicin overdose and in monitoring levels of gentamicin to help ensure appropriate therapy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2151-2020·2020-06-03
Biomet Vanguard Knee System Recalled for Elevated Endotoxin Levels
Biomet, Inc. is recalling 11 units of Vanguard Knee System tibial bearings due to potential endotoxin levels exceeding specification limits.
Product
Knee Products: 189260 Vanguard Knee System, CR-L Mono Lock Tibial Bearing, 10 MM X 71 MM 189720 Vanguard Knee System, CR Mono Lock Tibial Bearing, 10 MM X 83 MM 189320 Vanguard Knee System, CR-L Mono Lock Tibial Bearing, 10 MM X 83 MM 189700 Vanguard Knee System, CR Mono…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2163-2020·2020-06-03
Hologic Panther Fusion Extraction Reagent-S Recalled for False Test Results
Hologic is recalling Panther Fusion Extraction Reagent-S kits because a reagent component may cause false positive or negative flu test results, potentially delaying treatment.
Product
Panther Fusion Extraction Reagent-S, Ref PRD-04331, IVD, CE, Rx Only consisting of FCR-S Fusion Capture Reagent - S, Nucleic Acid in a buffered solution and FER-S Fusion Enhancer Reagent-S (Lithium Hydroxide Solution), UDI: 15420045509214
Category
Medical Device
Distribution
15 states
ModerateFDA (Devices)·Z-2141-2020·2020-06-03
Inpeco Accelerator a3600 Automation System Recalled for Sample Association Errors
Inpeco S.A. is recalling three Accelerator a3600 Automation Systems due to a firmware communication error that can cause incorrect sample-tube associations.
Product
Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01, FLX-226-10), or StaRRsed Interface Module (P/N FLX-268-00) is a modular system designed to automate Pre-Analytical and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2108-2020·2020-06-03
Siemens ARTIS Pheno X-Ray Systems Recalled for Drivetrain Faults
Siemens is recalling 105 ARTIS Pheno X-ray systems because a drivetrain fault may prevent the C-arm from moving, requiring field service to restore operation.
Product
ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 - Product Usage: is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2106-2020·2020-06-03
Medtronic Guardian Connect App iOS Recall for Battery Life Issues
Medtronic is recalling the Guardian Connect App for iOS due to shortened transmitter battery life on specific iPhone, iPad, and iPod Touch devices.
Product
Guardian Connect App CSS7200 iOS and Guardian Connect Transmitter GST4C used on the iPhone, iPad and iPod Touch devices.
Category
Medical Device
Distribution
Distributed nationwide