State

US Virgin Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38426–38450 of 73916

SevereFDA (Devices)·Z-1834-2018·2018-05-23
Medtronic Endo GIA Universal Staplers Recalled for Missing Sled Component
Medtronic is recalling Endo GIA Universal staplers because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
BOX KIT1171C KIT LAP CYSTECTOMY Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is determined…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1844-2018·2018-05-23
Medtronic Endo GIA Staplers Recalled for Missing Sled Component
Medtronic is recalling Endo GIA universal staplers because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
BOX LAPIMBGP1 ZESTAW DO MGBP (LAPIMBGP1) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V338000·2018-05-23
Kia Recalls 2015-2018 Sedona Vehicles Due to Power Sliding Door Defect
Kia is recalling 2015-2018 Sedona vehicles because the power sliding door may not auto-reverse if obstructed, increasing injury risk.
Product
KIA — KIA SEDONA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1854-2018·2018-05-23
Medtronic Endo GIA Universal Staplers Recalled for Missing Sled Component
Medtronic is recalling Endo GIA Universal and Universal XL staplers because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
BOX PST03699 KIT APP MED ALTERNATIV STAP Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1805-2018·2018-05-23
Zimmer Biomet Recalls Persona Stemmed Tibial Provisional Instruments
Zimmer Biomet is recalling 842 Persona Stemmed Tibial Provisional instruments due to potential cracks in the raw material that could compromise cleanliness.
Product
Persona Stemmed Tibial Provisional Size H Left, Item Number 42532108301 For use during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1812-2018·2018-05-23
Tosoh HbA1c Pretreatment Solution Recalled for Potential Inaccurate Test Results
Tosoh Bioscience Inc is recalling HbA1c Pretreatment Solution because it may cause erroneously elevated or decreased patient test results.
Product
Tosoh ST AIA-PACK HbA1c Pretreatment Solution, HbA1c Pretreatment Solution, PN 025718 The device is intended for In Vitro Diagnostic Use Only for the pretreatment of the patient samples or control set for the HbA1c assay
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1808-2018·2018-05-23
Zimmer Biomet Recalls Persona Cemented Tibial Plate Due to Cracks
Zimmer Biomet is recalling 842 Persona Cemented Tibial Plate units because potential cracks in the raw material could compromise the cleanliness of the instruments.
Product
Persona Cemented Tibial SZ PLT Size H Right, Item Number 42539908302 For use during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V337000·2018-05-23
Land Rover Recalls 2017 Models for Fuel Gauge Software Error
Jaguar Land Rover is recalling 2017 Range Rover, Range Rover Sport, and Discovery vehicles because a software error may cause the engine to shut off unexpectedly.
Product
LAND ROVER — LAND ROVER RANGE ROVER SPORT, DISCOVERY, RANGE ROVER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1871-2018·2018-05-23
Kelyniam Custom Skull Implant Recalled for Unvalidated Design Changes
Kelyniam Global is recalling 16 Custom Skull Implants because significant design changes were not validated or submitted to the FDA for marketing clearance.
Product
Kelyniam Custom Skull Implant (CSI), Model no. PEEK-IM1002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1813-2018·2018-05-23
Draeger Infinity Acute Care System Recalled for Software Anomaly
Draeger Medical Systems is recalling the Infinity Acute Care System due to a software anomaly that can cause loss of patient settings and stored data.
Product
Infinity Acute Care System (lACS) Monitoring Solution; Catalog Numbers:MS20401, MS20724, MS22956, MS25510, MS25520, MS25643, MS26196, MS26372, MS31818; UDI Information: 4049098054454, 4049098054447, 4049098054409, 4049098009799, 4049098009751. Multi-parameter, physiologic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1872-2018·2018-05-23
Kelyniam Custom Skull Implant Recall for Unvalidated Design Changes
Kelyniam Global is recalling 23 Custom Skull Implants because significant design changes were not validated or submitted to the FDA for clearance.
Product
Kelyniam Custom Skull Implant (CSI), Model no. PEEK-IM1003
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18165·2018-05-23
Kohler Recalls Automatic Transfer Switches for Generators Due to Fire Hazard
Kohler is recalling about 6,600 automatic transfer switches for generators because they can overheat and cause fires. No injuries have been reported.
Product
Kohler 100-amp service-entrance automatic transfer switches
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1833-2018·2018-05-23
Medtronic Endo GIA Universal Stapler Kits Recalled for Missing Sled Component
Medtronic is recalling Endo GIA Universal stapler kits because a missing sled component may prevent staple formation, risking bleeding or leakage.
Product
BOX KIT00714 KIT SLEEVE Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is determined by the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1870-2018·2018-05-23
Kelyniam Custom Skull Implant Recalled for Unvalidated Design Changes
Kelyniam Global is recalling two Custom Skull Implants because significant design changes were not validated or submitted to the FDA for marketing clearance.
Product
Kelyniam Custom Skull Implant (CSI), Model no. PEEK-IM1001 (Small)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1867-2018·2018-05-23
Invivo Xper Flex Cardio Physiomonitoring System Recalled for Inaccurate Pressure Readings
Invivo is recalling 4,375 Xper Flex Cardio Physiomonitoring Systems because ventricular end-diastolic pressure readings may be inaccurate. The issue affects specific model numbers used in cardiac catheterization rooms.
Product
PHILIPS Xper Flex Cardio Physiomonitoring System, Model Numbers: 453564241901, 453564483321, 453564621791, and 989803199561 (international only) The Xper Flex Cardio physiomonitoring system is used to facilitate invasive investigation of heart and vascular, disease when…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1803-2018·2018-05-23
Bard Peripheral Vascular Seeker Crossing Support Catheter Recalled for Endotoxin Risk
Bard Peripheral Vascular Inc is recalling 130 units of Seeker Crossing Support Catheters due to potential bacterial endotoxin on packaging hoops, posing a cross-contamination risk.
Product
BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter, 0.014", 150 cm, REF SK15014. Intended to support a guidewire during access into the vasculature.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1809-2018·2018-05-23
Tosoh Bioscience Recalls HbA1c Reagent Due to Potential Test Errors
Tosoh Bioscience Inc is recalling Tosoh ST AIA-PACK HbA1c reagents because the assay may produce erroneously high or low Hemoglobin A1c results.
Product
Tosoh ST AIA-PACK HbA1c, HbA1c Reagent, Pt. No. 025218 The device is designed for In Vitro Diagnostic Use Only for the quantitative measurement for percent concentration of Hemoglobin A1c (HbA1c) in EDTA whole blood on Tosoh AIA System Analyzer. HbA1c measurement is used in…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V333000·2018-05-23
Forest River Recalls Vengeance Trailers for Missing Side Marker Lights
Forest River is recalling 2017-2019 Vengeance Rouge recreational trailers because they may be missing side marker lights, reducing visibility to other drivers.
Product
FOREST RIVER — FOREST RIVER VENGEANCE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1873-2018·2018-05-23
Kelyniam Custom Skull Implant Recalled for Unvalidated Design Changes
Kelyniam Global is recalling 54 Custom Skull Implants because significant design changes were not validated or submitted to the FDA for clearance.
Product
Kelyniam Custom Skull Implant (CSI), Model no. PEEK-IM1004
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1829-2018·2018-05-23
Medtronic Endo GIA Universal Staplers Recalled for Missing Sled Component
Medtronic is recalling Endo GIA Universal staplers because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
(1) BOX BOX1073180 APPE1 APPENDIX KIT ZAMS (Item Code BOX1073180) (2)BOX BOX1073180APPE1 APPENDIX KIT ZAMS (Item Code BOX1073180APPE1 APPENDIX KIT ZAMS) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1818-2018·2018-05-23
Medtronic Endo GIA Stapler Loading Units Recalled for Missing Sled Component
Medtronic is recalling 171,271 Endo GIA Auto Suture Universal Articulating Loading Units because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm- 3.5mm( Item Code 030455) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1806-2018·2018-05-23
Zimmer Biomet Recalls Persona Stemmed Tibial Provisional Instruments
Zimmer Biomet is recalling 842 Persona Stemmed Tibial Provisional instruments due to potential raw material cracks that could compromise cleanliness.
Product
Persona Stemmed Tibial Provisional Size H Right, Item Number 42532108302 For use during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1811-2018·2018-05-23
Tosoh Bioscience Recalls HbA1c Control Due to Erroneous Results
Tosoh Bioscience Inc is recalling Tosoh ST AIA-PACK HbA1c Control because the product may generate erroneously elevated or decreased HbA1c patient results.
Product
Tosoh ST AIA-PACK HbA1c Control, HbA1c Control, PN 025418 The product is intended for In Vitro Diagnostic Use Only for performing quality control procedures with the HbA1c Assay.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1810-2018·2018-05-23
Tosoh HbA1c Calibrator Recalled for Potential Inaccurate Patient Results
Tosoh Bioscience Inc is recalling HbA1c Calibrators because they may cause erroneous patient test results.
Product
Tosoh ST AIA-PACK HbA1c Calibrator, HbA1c Calibrator, PN 025318 The product is intended for In Vitro Diagnostic Use Only for the calibration of the HbA1c Assay.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1889-2018·2018-05-23
Ethicon 5mm Endopath Xcel Trocar Recalled for Lubrication Defect
Ethicon Endo-Surgery Inc is recalling 5mm Endopath Xcel trocars due to insufficient lubrication, which may prolong surgery or introduce minute particles.
Product
5mm Endopath Xcel with Optiview Technology, Universal Trocar with Stability Sleeve, 5mm, 75mm shaft length, 2CB5ST
Category
Medical Device
Distribution
Distributed nationwide