The Recall Desk

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.

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.

40926–40950 of 73919

  • SevereNHTSA·17V625000·2017-10-06

    Subaru Recalls 2015 WRX Models Due to Subwoofer Wiring Fire Risk

    Subaru is recalling 9,178 2015 WRX vehicles because trunk items may cause subwoofer wiring to short, potentially leading to overheating and fire.

    Product
    SUBARU — SUBARU WRX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V632000·2017-10-06

    John Evans Recalls 2017-2018 Flatbed Trailers Due to Brake Defect

    John Evans is recalling 2017-2018 Flatbed trailers because air brake diaphragms may degrade, causing emergency brakes to engage and increasing crash risk.

    Product
    EVANS — EVANS FLATBED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V623000·2017-10-06

    Forest River Berkshire Buses Recalled for Headlight Failure

    Forest River is recalling 2014-2017 Berkshire XL and XLT buses because headlights may shut off when switching beams, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V627000·2017-10-06

    Mercedes-Benz Recalls Vehicles for Driver Air Bag Deployment Risk

    Mercedes-Benz is recalling 495,290 vehicles because the driver's air bag may deploy unexpectedly due to insufficient grounding, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG C43, GLK350, GLK250, C250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V630000·2017-10-05

    Cheetah Trailer Chassis Recalled for Air Brake Diaphragm Defect

    Cheetah Chassis Corporation is recalling specific 2017-2018 trailer chassis models because air brake diaphragms may degrade, causing emergency brakes to engage unexpectedly.

    Product
    CHEETAH — CHEETAH MAXIMIZER CHASSIS, TANK CHASSIS, BRIDGEMASTER CHASSIS, EXTENDABLE CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V622000·2017-10-05

    Audi Recalls 2013-2016 Models Due to Auxiliary Heater Fire Risk

    Volkswagen Group of America is recalling 216,913 Audi A5, A4 Allroad, and Q5 vehicles because contact corrosion in the auxiliary heater connector may cause wires to overheat or melt, increasing the risk of a fire.

    Product
    AUDI — AUDI A5, A4 ALLROAD, Q5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V621000·2017-10-05

    GM Recalls 2015-2016 Vehicles for Driver Air Bag Defect

    General Motors is recalling 2015-2016 Chevrolet Colorado, GMC Canyon, and 2016 Chevrolet Volt vehicles because the driver's frontal air bag may inflate improperly during a high-speed crash.

    Product
    CHEVROLET — CHEVROLET, GMC VOLT, COLORADO, CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3164-2017·2017-10-04

    Zimmer Biomet Recalls ECT Internal Fracture Fixation Drills

    Zimmer Biomet is recalling 4,423 ECT Internal Fracture Fixation Drills because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    ECT Internal Fracture Fixation Drill 2.0 mm Diameter (.079 Inch), Item Number/EDI 00231802000, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3181-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Surgical Drills and Screw Taps

    Zimmer Biomet is recalling 1,129 orthopedic surgical drills and screw taps due to raw material anomalies that may increase the risk of instrument fracture.

    Product
    Zimmer Periarticular Locking Plate System Drill Standard 2.7 mm Diameter, Item Number/EDI 00236020527, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3183-2017·2017-10-04

    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
    ECT Internal Fracture Fixation Quick-Connect Drill 2.0 mm Diameter 12.5 cm Length, Item Number/EDI 00241002100, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3151-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Surgical Drill Bits and Screw Taps

    Zimmer Biomet is recalling specific orthopedic surgical instruments due to a raw material anomaly that may increase the risk of instrument fracture during use.

    Product
    Zimmer Natural Nail System Calibrated Drill Long 4.3mm, Item Number/EDI 00249004443, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1177-2017·2017-10-04

    Pfizer Recalls Sterile Water for Injection Vials Due to Cracked Glass

    Pfizer is recalling 18,725 vials of Sterile Water for Injection due to cracked or chipped glass at the neck, which poses a non-sterility risk.

    Product
    Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3196-2017·2017-10-04

    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 3.5 mm Diameter 110 mm Length, Item Number/EDI 00480611035, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V618000·2017-10-04

    Prevost Recalls Motor Coaches Due to Fuel Tank Cradle Defect

    Prevost is recalling 2008-2018 motor coaches because fuel tank cradles may loosen, causing the tank to fall off and increasing crash risk.

    Product
    PREVOST — PREVOST XL2, H3-41, X3-45 VIP ENTERTAINER, X3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3106-2017·2017-10-04

    Spectranetics Bridge Occlusion Balloon Catheter Recalled for Guidewire Issues

    Spectranetics is recalling Bridge Occlusion Balloon catheters because the guidewire may not pass through the device, potentially delaying treatment.

    Product
    Spectranetics Bridge Occlusion Balloon catheter, Sheath Compatibility 12F, Guidewire Compatibility 0.035in, Working Length 90cm, Balloon Outer Diameter 31mm, Balloon Length 80mm, Rx Only. Product Usage: It is a device used to occlude the vessel and prevent blood loss as the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3175-2017·2017-10-04

    Zimmer Biomet Recalls Straight Shank Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 62 units of 4.0 mm Straight Shank Drill Bits because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    Straight Shank Drill Bits 4.0 mm Diameter, Item Number/EDI 00231804006, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3202-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 150 nonsterile orthopedic drill bits because raw material anomalies may cause the instruments to fracture during use.

    Product
    Drill Bit Quick-Connect 4.5 mm Diameter 145 mm Length, Item Number/EDI 00480614545, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3199-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 15 nonsterile orthopedic drill bits because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    Drill Bit Quick-Connect 3-Fluted 4.5 mm Diameter 195 mm Length, Item Number/EDI 00480719545, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3231-2017·2017-10-04

    Sorin Platinium VR ICDs Recalled for Potential Overconsumption Risk

    Sorin Group is recalling 72 Platinium VR implantable cardioverter defibrillators due to a possibility of overconsumption following electrostatic discharge or MRI scans.

    Product
    Platinium VR DF4 1240, Model Number TDF035U, UDI/GTIN 08031527015460, Implantable cardioverter defibrillator, Biventricular or ventricular antitachycardia pacing, Dual or single chamber arrhythmia detection Product Usage: PLATINIUM VR is indicated for use in patients…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3167-2017·2017-10-04

    Zimmer Biomet Recalls ECT Internal Fixation Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling ECT Internal Fixation Drill Bits because raw material anomalies may cause the instruments to fracture during use.

    Product
    ECT Internal Fixation Drill Bits 2.5 mm Diameter (0.98 Inch), Item Number/EDI 00231802506, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3158-2017·2017-10-04

    Zimmer Biomet Recalls M/DN Intramedullary Fixation Distal Drill Pilot Tips

    Zimmer Biomet is recalling 182 M/DN Intramedullary Fixation Distal Drill Pilot Tips due to raw material anomalies that may increase the risk of instrument fracture.

    Product
    M/DN Intramedullary Fixation Distal Drill Pilot Tip 3.2 mm Diameter, Item Number/EDI 00225503332, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V617000·2017-10-04

    Hyundai Sonata Seat Belt Linkage Recall for Detachment Risk

    Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles previously repaired under a prior campaign because seat belt linkages may detach from pretensioners, increasing injury risk in a crash.

    Product
    HYUNDAI — HYUNDAI SONATA HYBRID, SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide