The Recall Desk

State

US Virgin Islands product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28076–28100 of 73762

  • HighNHTSA·20V468000·2020-08-10

    Entegra Qwest motorhome wiring defect may cause airbag malfunction

    Jayco is recalling 2020-2021 Entegra Qwest motorhomes and related Jayco models because front seat wiring harnesses may be routed incorrectly, creating a risk of unexpected or failed airbag deployment.

    Product
    JAYCO — JAYCO, ENTEGRA MELBOURNE PRESTIGE, QWEST, MELBOURNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V464000·2020-08-07

    Mercedes-Benz Recalls 2020 GLE 450 for Windshield Bonding Defect

    Mercedes-Benz is recalling one 2020 GLE 450 because the windshield may not be bonded correctly, which could reduce the effectiveness of the passenger air bag in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V463000·2020-08-07

    American Hauler Recalls 2018 Trailers Due to Axle Weld Failures

    American Hauler is recalling 2018 Air-Lite, Arrow, Falcon/XC, and Night Hawk trailers because spindle weld failures on the axles may increase the risk of a crash or injury.

    Product
    AMERICAN HAULER — AMERICAN HAULER NIGHT HAWK, AIR-LITE, FALCON/XC, ARROW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V466000·2020-08-07

    2017-2021 Freightliner Business Class M2 trucks recalled for electrical harness defect

    Daimler Trucks North America is recalling certain 2017-2021 Freightliner Business Class M2 trucks because the engine harness may contact and chafe, potentially short-circuiting and causing engine stall during operation.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V465000·2020-08-07

    BMW Recalls 2020 X5 and X7 Models Due to Starter Motor Bolt Risk

    BMW is recalling 21 vehicles because an extra bolt in the starter motor could fall into the transmission, causing an engine stall and increasing crash risk.

    Product
    BMW — BMW X7, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V461000·2020-08-06

    GM Recalls 2020 Chevrolet Corvette for Front Trunk Release Defect

    General Motors is recalling 2020 Chevrolet Corvette vehicles because the front trunk release button may fail to function after the vehicle is shut off for ten minutes, potentially trapping a person inside.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20769·2020-08-06

    REVIVE Essential Oils Recalled for Non-Child-Resistant Packaging and Poisoning Risk

    REVIVE is recalling specific essential oils and blends because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.

    Product
    REVIVE Wintergreen and Birch Essential Oils and REVIVE Sore No More, Ache Away and Breeze Essential Oil Blends
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2729-2020·2020-08-05

    Teleflex Medical Recalls Rusch Greenlite Laryngoscopes Due to Welded Joint Breakage

    Teleflex Medical is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The recall covers 20,600 units distributed nationwide.

    Product
    Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2738-2020·2020-08-05

    Hill-Rom Recalls 1,033 Centralia Smart+ Beds Due to Screw Defect

    Hill-Rom is recalling 1,033 Centralia Smart+ Beds because screws may not meet tensile strength requirements, posing a risk of serious injury.

    Product
    Centrella Smart+ Bed, Catalog No. P7900 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2737-2020·2020-08-05

    Hill-Rom Recalls Progressa Beds Due to Screw Tensile Strength Defect

    Hill-Rom is recalling 257 Progressa Beds because screws may not meet tensile strength requirements, posing a risk of serious injury to patients or users.

    Product
    Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V456000·2020-08-05

    Blue Bird Recalls 2021 School Buses Due to Steering Wheel Nut Issue

    Blue Bird is recalling 2021 Vision and All American school buses because the steering wheel nut may not be tightened properly, risking loss of control.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V455000·2020-08-05

    Blue Bird Recalls 2021 Transit Buses Due to Steering Wheel Nut Issue

    Blue Bird is recalling 2021 Vision and All American transit buses because the steering wheel nut may not be properly tightened, risking loss of vehicle control.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, ALL AMERICAN TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1412-2020·2020-08-05

    Saniderm Hand Sanitizer Recalled for Undeclared Methanol and Low Ethanol

    Polarized LLC is recalling Saniderm Advanced Hand Sanitizer because it contains undeclared methanol and less ethanol than labeled.

    Product
    Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by Eskbiochem SA de CV, Mexico Japon 50, Celaya, Gto., Mexico, 38010. UPC 8 60003 63391 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2742-2020·2020-08-05

    OrthoPediatrics Recalls Spine Rods Due to Potential Fracture Risk

    OrthoPediatrics Corp is recalling 73 units of 6.0MM spine rods because incorrect laser etching may compromise strength and lead to unintended fracture.

    Product
    Orthopedics 6.0MM ROD, COCR, SINGLE HEX, 500MM LENGTH-The RESPONSE" 5.5/6.0 Spine System is intended for immobilization and stabilization of the posterior, non-cervical spine in skeletally mature patients as an adjunct to fusion for the following indications: degenerative disc…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1427-2020·2020-08-05

    MasterPharm Recalls Progesterone Capsules Due to Processing Control Deficiencies

    MasterPharm LLC is recalling 600 capsules of Progesterone (Modified Release) 150 mg due to a lack of processing controls.

    Product
    Progesterone (Modified Release) 150 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1407-2020·2020-08-05

    Saniderm Hand Sanitizer Recalled for Undeclared Methanol Contamination

    UVT INC is recalling Saniderm Advanced Hand Sanitizer because it contains undeclared methanol. The product was distributed nationwide in the USA.

    Product
    Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by Eskbiochem SA de CV, Mexico Japon 50, Celaya, Gto., Mexico, 38010. UPC 8 60003 63391 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V459000·2020-08-05

    Kia Recalls 2019 Forte Vehicles Due to Axle Driveshaft Defect

    Kia is recalling 2019 Forte vehicles because the left front axle driveshaft may not have been heat-treated, which can cause it to break and increase crash risk.

    Product
    KIA — KIA FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2725-2020·2020-08-05

    Medline Recalls ClearPro Trach T-Piece Closed Suction Catheters

    Medline is recalling 680 units of ClearPro Trach T-Piece Closed Suction Catheters because the catheter may come apart from the device assembly during use.

    Product
    ClearPro Trach T-Piece Closed Suction Catheter, Model DYNCPTP14T, 14 Fr 12.5 IN FOR TRACHEOSTOMY TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2708-2020·2020-08-05

    TTDEYE Black Starshine Colored Contact Lenses Recalled for Lack of FDA Clearance

    Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Black Starshine colored contact lenses because they were distributed without FDA clearance.

    Product
    TTDEYE (brand) Black Starshine, B16112100 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2726-2020·2020-08-05

    Teleflex Rusch Greenlite Laryngoscopes Recalled for Welded Joint Breakage

    Teleflex Medical Inc. is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The recall affects 75,320 units distributed nationwide.

    Product
    Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2712-2020·2020-08-05

    TTDEYE Radial Brown Colored Contact Lenses Recalled for Lack of FDA Clearance

    Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Radial Brown colored contact lenses because they were distributed without FDA clearance.

    Product
    TTDEYE (brand) Radial Brown, B16112109 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2707-2020·2020-08-05

    Medtronic StealthStation S7 System Recalled for Navigation Inaccuracy

    Medtronic is recalling two StealthStation S7 Systems with Polaris Spectra Cameras due to a manufacturing issue that may cause 6mm navigation inaccuracy when using specific trackers.

    Product
    StealthStation" S7 System with Polaris Spectra Camera part number PSU 9733437 - Product Usage: are intended as an aid for precisely locating anatomical structures in either open or percutaneous procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide