The Recall Desk

State

US Virgin Islands product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27526–27550 of 73754

  • HighNHTSA·20V616000·2020-10-06

    REV Recalls 2019 Road Rescue Type I Ambulances for Door Latch Defect

    REV Ambulance Group is recalling 2019 Road Rescue Type I ambulances because incorrect material in door latches may prevent doors from opening, creating a lock-in risk.

    Product
    ROAD RESCUE — ROAD RESCUE TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V611000·2020-10-05

    Yamaha Recalls YZF-R3, XMAX, and MT-03 Models for Rear Reflector Defect

    Yamaha is recalling specific 2015-2020 motorcycles and scooters because condensation on the rear reflector lens may reduce its effectiveness, increasing crash risk.

    Product
    YAMAHA — YAMAHA YZF-R3, XMAX, redundant YZF-R3, MT-03
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V613000·2020-10-05

    Volvo Recalls 2020 VNL Trucks for Window Hinge Defect

    Volvo Trucks North America is recalling 2020 VNL vehicles because window hinges may fail if sleeper windows are open, posing a crash risk.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V607000·2020-10-02

    Mercedes-Benz Recalls 2020 GLC 350e for High-Voltage Wiring Harness Defect

    Mercedes-Benz is recalling 2020 GLC 350e hybrid vehicles because a high-voltage wiring harness shield may fail, causing an electrical malfunction and vehicle stall.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V610000·2020-10-02

    Micro Bird Recalls 2019 MB II Buses Due to Electrical Fire Risk

    Micro Bird is recalling 75 model-year 2019 MB II buses because a grounding wire issue may cause a short circuit, increasing the risk of fire.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E073000·2020-10-02

    Dick's Sporting Goods Recalls Field & Stream Kayak Cradles

    Dick's Sporting Goods is recalling Field & Stream Kayak Cradles because kayaks may fall off while driving, increasing crash risk.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V605000·2020-10-02

    2021 Motorhome Bunk Bed Motor May Fail, Causing Bunk to Fall

    The P2K Bunk Bed System motor in certain 2021 Coachmen Sportscoach and Forest River Georgetown motorhomes may fail, causing the bunk to fall while the vehicle is in motion. This increases the risk of injury or a crash.

    Product
    COACHMEN — COACHMEN, FOREST RIVER SPORTSCOACH, GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V608000·2020-10-02

    Mercedes-Benz Recalls 2019 C 300 for Center Console Lock Defect

    Mercedes-Benz is recalling 2019 C 300 vehicles because the center console lock may not function properly, increasing injury risk in rear-end crashes.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V604000·2020-10-02

    Aston Martin Recalls Vehicles Due to Loose Front Seat Air Bag Fasteners

    Aston Martin is recalling specific 2017-2020 models because front seat air bag fasteners may not be tightened correctly, increasing injury risk.

    Product
    ASTON MARTIN — ASTON MARTIN VANTAGE, DB11, DBS SUPERLEGGERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V603000·2020-10-01

    GM Recalls 2018 Trucks and SUVs for Brake Assist Defect

    General Motors is recalling 2018 Cadillac, Chevrolet, and GMC vehicles because a vacuum pump issue can reduce power brake assist, increasing stopping distance.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, GMC SILVERADO 1500, ESCALADE, TAHOE, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1595-2020·2020-09-30

    Protein Shoppe Recalls Red-E Tablets Tainted With Sildenafil

    The Protein Shoppe is recalling Red-E Tablets found to contain sildenafil, an unapproved drug for erectile dysfunction. The product was marketed without FDA approval.

    Product
    Red-E Tablet, Proprietary Blend 3000 mg**, packaged in 1-count plastic bag stapled with cardboard labeling.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V599000·2020-09-30

    Ford Recalls 2020 F-350 Trucks Due to Rear Axle Mismatch

    Ford is recalling 2020 F-350 trucks with ambulance prep packages because incorrect rear axles were installed, creating a risk of tire blowouts.

    Product
    FORD — FORD redundant F-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3005-2020·2020-09-30

    Siemens Syngo.via RT Image Suite Software Recall for Calibration Offset Error

    Siemens is recalling Syngo.via RT Image Suite software due to a calibration offset error that could result in incorrect radiation dose or dose applied to the wrong location.

    Product
    Software: Syngo.via RT Image Suite software version VA30_SP02 with license T_RT_IMAGE_SUITE_PAT_MARK Intended Use: used as an advanced application on a SOM10 scanner SMN: 10496180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·20193·2020-09-30

    STIHL Recalls Mini-Cultivator Attachments Due to Laceration Hazard

    STIHL is recalling about 185,000 mini-cultivator attachments because the gearbox may be installed upside down, causing tines to rotate toward the operator and posing a laceration risk.

    Product
    STIHL BF-KM Mini-Cultivator attachments
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V598000·2020-09-30

    BMW 2020-2021 Rearview Camera Software Obscures Rear View Image

    BMW is recalling approximately 312 certain 2020-2021 BMW models due to rearview camera software that may slightly obscure the rear view image, potentially increasing crash risk if drivers rely solely on the camera.

    Product
    BMW — BMW 530I, X3, X4, M550I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2985-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling 94 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.

    Product
    Perceval Single Use Accessory Kit, Size M, REF: ICV1346, Sterile EO, Rx Only, CE, UDI: 8022057015228 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2984-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling 77 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.

    Product
    Perceval Single Use Accessory Kit, Size S, REF: ICV1345, Sterile EO, Rx Only, CE, UDI: 8022057015204 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V601000·2020-09-30

    BMW recalls vehicles due to debris in hybrid battery cells

    BMW is recalling certain 2020-2021 models due to debris in hybrid battery cells that could cause fire or injury. Owners are instructed not to charge vehicles or drive in manual mode.

    Product
    BMW — BMW, MINI 745LE, X5, 530E, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3012-2020·2020-09-30

    Irvine Biomedical Recalls Steerable Diagnostic Catheters Due to Labeling Error

    Irvine Biomedical is recalling 40 units of Inquiry Steerable Diagnostic Catheters because packages were mislabeled with the wrong model and lot numbers, potentially causing procedure delays.

    Product
    Inquiry Steerable Diagnostic Catheter, REF: IBI-87002 - Product Usage: INDICATIONS FOR USE The Inquiry fixed curve and steerable electrophysiology catheters are used for electrogram recording and cardiac stimulation during diagnostic electrophysiology studies. The catheters are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2986-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling 102 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.

    Product
    Perceval Single Use Accessory Kit, Size S, REF: ICV1349, Sterile EO, Rx Only, CE, UDI: 8022057015211 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20194·2020-09-30

    Petzl Recalls Low-Stretch Kernmantle Ropes Due to Fall and Injury Hazard

    Petzl is recalling approximately 14,850 low-stretch kernmantle ropes sold in the U.S. and Canada because deep cuts or tape securing rope ends can cause failure, posing fall and injury hazards.

    Product
    Low-Stretch Kernmantle Ropes
    Category
    Consumer Product
    Distribution
    Distributed nationwide