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.

28151–28175 of 73762

  • ModerateFDA (Drugs)·D-1437-2020·2020-08-05

    MasterPharm Recalls Tadalafil 18 mg Capsules Due to Processing Control Deficiencies

    MasterPharm LLC is recalling Tadalafil 18 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.

    Product
    Tadalafil 18 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1411-2020·2020-08-05

    Hand Sanitizer Recalled for Subpotent Alcohol and High pH Levels

    World Event Promotions, LLC is recalling Handese Advanced Instant Hand Sanitizer because the product was found to be subpotent and has high pH levels.

    Product
    Handese Advanced Instant Hand Sanitizer (Ethyl Alcohol 70%), 12 FL OZ (354 mL) bottles, www.handeseclean.com UPC 612520481094
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1445-2020·2020-08-05

    Sun Pharmaceutical Recalls Clonazepam Tablets Due to Cross-Contamination

    Sun Pharmaceutical is recalling Clonazepam Orally Disintegrating Tablets because routine stability testing detected cross-contamination with clozapine.

    Product
    Clonazepam Orally Disintegrating Tablets, USP, 0.125 mg, 60-count bottle, Rx only, Mfg by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, NDC 57664-783-86
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1421-2020·2020-08-05

    MasterPharm Recalls Estriol 8 mg Capsules Due to Processing Control Deficiencies

    MasterPharm LLC is recalling Estriol 8 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.

    Product
    Estriol 8 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2702-2020·2020-08-05

    Smith & Nephew T-F1X0 RCG Drill Pac Recalled for Missing Sleeve

    Smith & Nephew is recalling T-F1X0 RCG Drill Pacs because some sterile packages contain only one sleeve instead of two, preventing the device from performing as intended for the second bone tunnel.

    Product
    Smith & Nephew T-F1X0 RCG Drill Pac, 2 mm Drill & (2) Sleeves - Product Usage: indicated for use in surgical arthroscopic rotator cuff repair procedures. REF/ Catalog Number : 014771
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1422-2020·2020-08-05

    MasterPharm Recalls Finasteride Plus Capsules Due to Processing Control Deficiencies

    MasterPharm LLC is recalling Finasteride Plus 1.25mg capsules nationwide because the product lacked processing controls to ensure it met specifications.

    Product
    Finasteride Plus 1.25mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1433-2020·2020-08-05

    MasterPharm Recalls Progesterone Capsules Due to Processing Control Deficiencies

    MasterPharm LLC is recalling 600 capsules of Progesterone Modified Release 100 mg due to a lack of processing controls that ensures conformity to specifications.

    Product
    Progesterone Modified Release 100 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1441-2020·2020-08-05

    MasterPharm Recalls Testosterone/Anastrozole Pellets Due to Processing Control Deficiencies

    MasterPharm LLC is recalling Testosterone/Anastrozole Pellets 100/6 mg due to a lack of processing controls that ensures conformity to specifications.

    Product
    Testosterone/Anastrozole Pellet 100/6 mg, 100 pellets per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419 (866) 630-5600
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1410-2020·2020-08-05

    Allergan Recalls Skin Medica Acne System Kits for Subpotency

    Allergan is recalling 8,555 Skin Medica Acne System kits nationwide because the products failed potency tests at 12 and 24 months.

    Product
    Skin Medica Acne System, Contains: Purifying Foaming Wash (Salicylic Acid 2.0%), 5 fl oz.; Purifying Toner (Salicylic Acid 2.0%), 6 fl oz,; Acne Treatment Lotion (Benzoyl Peroxide 2.5%), 2 fl oz., Distributed in the U.S.A. by Allergan, Irvine, CA 92612, UPC 300234966005
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·20V454000·2020-08-04

    Indian Recalls 2019 Scout Motorcycles Due to Brake Performance Issues

    Indian Motorcycle is recalling 2019 Scout, Scout Sixty, and Scout Bobber models because trapped air in the brake system may reduce performance and increase crash risk.

    Product
    INDIAN — INDIAN SCOUT BOBBER, SCOUT, SCOUT SIXTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V453000·2020-08-04

    2019 Mercedes-Benz Sprinter Recalled for Fuel Pump Leak Risk

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because an open port on the fuel pump may leak fuel onto the roadway, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER (VS30)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V451000·2020-08-03

    Triumph Recalls 2020 Tiger 900 Models for Detaching Rear Reflectors

    Triumph is recalling 2020 Tiger 900 motorcycles because rear reflectors may detach, reducing visibility and increasing crash risk.

    Product
    TRIUMPH — TRIUMPH TIGER 900 RALLY, TIGER 900, TIGER 900 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V452000·2020-08-03

    Bentley Recalls 2020 Flying Spur for Rear Camera Moisture Issue

    Bentley is recalling 2020 Flying Spur vehicles because moisture can enter the rear camera holder, reducing image clarity and increasing crash risk.

    Product
    BENTLEY — BENTLEY FLYING SPUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-08012020·2020-08-01

    USDA Alert: Frozen Taquitos and Chimichangas May Contain Hard Plastic

    USDA FSIS issued a public health alert for frozen taquitos and chimichangas that may contain hard plastic from recalled green chilies.

    Product
    Ajinomoto Foods North America — FSIS Issues Public Health Alert for Meat and Poultry Taquitos and Chimichangas Containing FDA-Regulated Diced Green Chilies That Have Been Recalled Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V447000·2020-07-31

    Hyundai Recalls 2020 Genesis G70 for Steering Locking Risk

    Hyundai is recalling 2020 Genesis G70 vehicles because a steering component may be defective, potentially causing the steering to lock or become difficult to operate while driving.

    Product
    HYUNDAI — HYUNDAI GENESIS G70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V449000·2020-07-31

    Mercedes-Benz Recalls Vehicles for Seat Belt Warning Software Defect

    Mercedes-Benz is recalling specific 2017-2019 models because instrument cluster software may cause the seat belt warning system to display a solid light instead of a blinking light with an audible tone.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS 450, E 300, C 300, E 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V450000·2020-07-31

    Autocar Xpeditor Parking Brake May Apply Unexpectedly

    Certain 2018-2021 Autocar Xpeditor right-hand drive trucks may have improperly assembled parking brake plumbing, causing the brake to apply unexpectedly and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E053000·2020-07-31

    Walmart Recalls Hyper Tough 2 Ton Jack Stands Due to Collapse Risk

    Walmart is recalling specific Hyper Tough 2 Ton Jack Stands that may collapse unexpectedly under load, posing a risk of injury to nearby persons.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E052000·2020-07-30

    ZF Recalls Air Bag Crash Sensors in Chrysler and Volkswagen Vehicles

    ZF is recalling air bag crash sensors in 2019 Chrysler Jeep Cherokee and 2018 Volkswagen Atlas vehicles due to manufacturing defects that may delay or prevent air bag deployment.

    Product
    AIR BAGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V446000·2020-07-30

    GM Recalls 2020 Vehicles Due to Roof-Rail Air Bag Defect

    General Motors is recalling 2020 Buick, Cadillac, Chevrolet, and GMC vehicles because the roof-rail air bag inflator may separate during deployment, increasing injury risk.

    Product
    GMC — GMC, CHEVROLET, CADILLAC SIERRA 1500, SILVERADO 3500, SILVERADO 1500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1408-2020·2020-07-29

    Mystic Shield Hand Sanitizer Recalled for Undeclared Methanol

    Transliquid Technologies is recalling Mystic Shield hand sanitizer bottles due to the presence of undeclared methanol.

    Product
    Mystic Shield PROTECTION, ALCOHOL ANTISEPTIC 70%, Topical Solution, Antiseptic Hand Rub, Non-sterile Solution, Extra strength Formula*, 8.45 fl. oz. (250 ml) bottle, Labeled with green or blue labels, Manufactured by Mystic Intl S.A. de C.V. UPC barcode: 7 87790 33952 6
    Category
    Drug
    Distribution
    Distributed nationwide