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.

40951–40975 of 73919

SevereFDA (Devices)·Z-3228-2017·2017-10-04
Sorin Platinium VR ICDs Recalled for Potential Overconsumption Risk
Sorin Group is recalling Platinium VR implantable cardioverter defibrillators due to a possibility of overconsumption following electrostatic discharge or MRI scans.
Product
Platinium VR 1210, Model Number TDF031U, UDI/GTIN 08031527015514, Implantable cardioverter defibrillator, Biventricular or ventricular antitachycardia pacing, Dual or single chamber arrhythmia detection Product Usage: PLATINIUM VR is indicated for use in patients who…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3187-2017·2017-10-04
Zimmer Biomet Recalls ECT Quick-Connect Drills Due to Fracture Risk
Zimmer Biomet is recalling 62 ECT Internal Fracture Fixation Quick-Connect Drills because raw material anomalies may cause the instruments to fracture during use.
Product
ECT Internal Fracture Fixation Quick-Connect Drill 3.5 mm Diameter 11 cm Length, Item Number/EDI 00241003500, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V619000·2017-10-04
Lexus Recalls 2010 HS 250h Hybrid for Transaxle Short Circuit Risk
Toyota is recalling 2010 Lexus HS 250h Hybrid vehicles because a hybrid transaxle component may short circuit, causing a loss of power and increasing crash risk.
Product
LEXUS — LEXUS HS 250 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3191-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may cause the instruments to fracture during use.
Product
Drill Bit Jacobs Chuck 3.2 mm Diameter 130 mm Length, Item Number/EDI 00480513032, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3188-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fracture Fixation Quick-Connect Drill Bits
Zimmer Biomet is recalling 10 units of ECT Internal Fracture Fixation Quick-Connect Drills due to a raw material anomaly that may increase the risk of instrument fracture during use.
Product
ECT Internal Fracture Fixation Quick-Connect Drill 4.0 mm Diameter 20cm Length, Item Number/EDI 00241004000, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3157-2017·2017-10-04
Zimmer Biomet Recalls NCB Periprosthetic Plate System Drill Bits
Zimmer Biomet is recalling 185 NCB Periprosthetic Plate System Drill Bits due to a raw material anomaly that may increase the risk of instrument fracture during use.
Product
NCB Periprosthetic Plate System Drill Bit With Quick-Coupling 4.5 mm Diameter 195 mm Length, Item Number/EDI 0200024330, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V620000·2017-10-04
Grand Design Recalls 2017-2018 Imagine Trailers for Fire Risk
Grand Design RV is recalling 2017-2018 Imagine recreational trailers because air conditioning wires may detach and short circuit, increasing fire risk.
Product
GRAND DESIGN — GRAND DESIGN IMAGINE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3150-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fracture Fixation Quick-Connect Drills
Zimmer Biomet is recalling 4 units of ECT Internal Fracture Fixation Quick-Connect Drills due to raw material anomalies that may increase the risk of instrument fracture.
Product
ECT Internal Fracture Fixation Quick-Connect Drill, 1.5 mm Diameter, 85mm Length, Item Number/EDI 00241001500, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3178-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Screw Taps Due to Material Anomaly
Zimmer Biomet is recalling 198 nonsterile orthopedic screw taps because raw material anomalies may increase the risk of instrument fracture during use.
Product
Zimmer Periarticular Locking Plate System, Locking Screw Tap Standard Quick-Connect 3.5 mm Diameter, Item Number/EDI 00236015335, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3160-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Surgical Instruments Due to Fracture Risk
Zimmer Biomet is recalling 21 units of M/DN Intramedullary Fixation Femoral Drills because raw material anomalies may cause the instruments to fracture during use.
Product
M/DN Intramedullary Fixation Femoral Drill Large 5.0 mm Item Number/EDI 00225503550, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3180-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Surgical Drills Due to Fracture Risk
Zimmer Biomet is recalling 1,091 nonsterile orthopedic surgical drills and screw taps because raw material anomalies may cause instrument fracture.
Product
Zimmer Periarticular Locking Plate System Drill Standard 2.0 mm Diameter, Item Number/EDI 00236017520, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3193-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because a raw material anomaly may increase the risk of instrument fracture during use.
Product
Drill Bit Quick-Connect 2.0 mm Diameter 100 mm Length, Item Number/EDI 00480610020, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3162-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fracture Fixation Drills Due to Material Anomaly
Zimmer Biomet is recalling 1,999 ECT Internal Fracture Fixation Drills because raw material anomalies may increase the risk of instrument fracture during use.
Product
ECT Internal Fracture Fixation Drill 1.5 mm Diameter (.059 Inch), Item Number/EDI 00231801500, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3200-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling 453 nonsterile orthopedic drill bits because raw material anomalies may cause instrument fracture during use.
Product
Drill Bit Quick-Connect Calibrated 3-Fluted 2.5 mm Diameter 230 mm Length, Item Number/EDI 00480723025, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·17V624000·2017-10-04
Transtech Recalls 2015-2016 School Buses Due to Seat Padding Defect
Transportation Collaborative is recalling 2015-2016 Trans Tech school buses because seat mounting studs lack adequate padding, increasing injury risk in rear-end collisions.
Product
TRANS TECH BUS — TRANS TECH BUS ST AERO, SST FLR, STUDENT SAFETY TRANSPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3156-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fracture Fixation Long Drills
Zimmer Biomet is recalling 10 units of ECT Internal Fracture Fixation Long Drills due to raw material anomalies that may increase the risk of instrument fracture.
Product
ECT Internal Fracture Fixation Long Drill, 6.4 mm (1/4 Inch) Diameter 20.3 cm(8 Inch) Length, Item Number/EDI 00129100406, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3170-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fracture Fixation Drill Bits
Zimmer Biomet is recalling 1,255 ECT Internal Fracture Fixation Drill Bits due to raw material anomalies that may increase the risk of instrument fracture during use.
Product
ECT Internal Fracture Fixation Drill 3.2 mm Diameter (.126 Inch), Item Number/EDI 00231803200, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3147-2017·2017-10-04
Zimmer Biomet Recalls M/DN Intramedullary Fixation Femoral Drill Bits
Zimmer Biomet is recalling 25 units of M/DN Intramedullary Fixation Femoral Drills due to raw material anomalies that may increase the risk of instrument fracture during use.
Product
M/DN Intramedullary Fixation Femoral Drill 3.7 mm Diameter Replaces 2255-08-32, Item Number/EDI 00225503137, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3194-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may increase the risk of instrument fracture during use.
Product
Drill Bit Quick-Connect 2.7 mm Diameter 100 mm Length, Item Number/EDI 00480610027, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3179-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Surgical Instruments Due to Material Anomaly
Zimmer Biomet is recalling 173 orthopedic surgical instruments because a material anomaly may increase the risk of instrument fracture during use.
Product
Zimmer Periarticular Locking Plate System Cannulated Drill Standard Quick-Connect 2.7 mm O.D., Item Number/EDI 00236017127, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3192-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling 705 nonsterile orthopedic drill bits and screw taps because raw material anomalies may cause instrument fracture during use.
Product
Drill Bit Quick-Connect 1.5 mm Diameter 85 mm Length, Item Number/EDI 00480608515, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3153-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling 25 nonsterile orthopedic drill bits because raw material anomalies may increase the risk of instrument fracture during use.
Product
Drill Bit Quick-Connect 1.1 mm Diameter 60 mm Length, Item Number/EDI 00480606011, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3182-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling 418 ECT Internal Fracture Fixation Quick-Connect Drills because raw material anomalies may increase the risk of instrument fracture during use.
Product
ECT Internal Fracture Fixation Quick-Connect Drill 2.0 mm Diameter 10 cm Length, Item Number/EDI 00241002000, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3154-2017·2017-10-04
Zimmer Biomet Recalls NCB Periprosthetic Plate System Drill Bits
Zimmer Biomet is recalling 300 nonsterile NCB Periprosthetic Plate System Drill Bits due to raw material anomalies that may increase the risk of instrument fracture during use.
Product
NCB Periprosthetic Plate System Drill Bit With Quick-Coupling 3.5 mm Diameter 195 mm Length, Item Number/EDI 0200024325, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3229-2017·2017-10-04
Sorin Platinium ICDs Recalled for Potential Overconsumption Risk
Sorin Group Italia SRL is recalling Platinium DR 1510 ICDs due to a possibility of overconsumption following ElectroStatic Discharge (ESD) during implant surgery or MRI scans.
Product
Platinium DR 1510, Model Number TDF032U, UDI/GTIN 08031527015521, Implantable cardioverter defibrillator, Biventricular or ventricular antitachycardia pacing, Dual or single chamber arrhythmia detection Product Usage: PLATINIUM VR is indicated for use in patients who…
Category
Medical Device
Distribution
Distributed nationwide