The Recall Desk

State

US Virgin Islands product recalls

73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30251–30275 of 73896

  • ModerateFDA (Devices)·Z-1041-2020·2020-02-12

    Implant Direct Sybron Recalls Legacy 3 Dental Implants Due to Incorrect Packaging

    Implant Direct Sybron is recalling 72 Legacy 3 dental implants because some packages contain incorrect implants, which could lead to surgery rescheduling.

    Product
    Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0990-2020·2020-02-12

    Cardinal Health Recalls Genius 2 Tympanic Thermometers for Accuracy Drift

    Cardinal Health is recalling Genius 2 Tympanic Thermometers because calibration frequency may not ensure readings stay within the stated accuracy range.

    Product
    Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0994-2020·2020-02-12

    Cardinal Health Genius 2 Tympanic Thermometer Recall for Accuracy Drift

    Cardinal Health is recalling Genius 2 tympanic thermometers because readings may drift upward over time, potentially exceeding the stated accuracy range.

    Product
    Genius 2 Tympanic Thermometer Private Label Item Code: 3069
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0992-2020·2020-02-12

    Cardinal Health Genius 2 Tympanic Thermometer Recall for Accuracy Drift

    Cardinal Health is recalling Genius 2 tympanic thermometers because readings may drift upward over time, potentially exceeding the stated accuracy range.

    Product
    Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0838-2020·2020-02-12

    Macleods Pharma Recalls Subpotent Pioglitazone and Metformin Tablets

    Macleods Pharma USA is recalling two lots of Pioglitazone and Metformin Hydrochloride tablets because they tested below the required potency levels.

    Product
    PIOGLITAZONE AND METFORMIN HYDROCHLORIDE — PIOGLITAZONE AND METFORMIN HYDROCHLORIDE (PIOGLITAZONE AND METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0830-2020·2020-02-12

    Teva Recalls Desmopressin Acetate Tablets Due to Missing Desiccant

    Teva Pharmaceuticals USA is recalling Desmopressin Acetate Tablets because bottles may be missing desiccant, a GMP deviation.

    Product
    Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2464-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0827-2020·2020-02-12

    Ascend Recalls Minocycline Hydrochloride Tablets for Dissolution Failures

    Ascend Laboratories is recalling Minocycline Hydrochloride Extended-Release Tablets due to low dissolution test results.

    Product
    MINOCYCLINE HYDROCHLORIDE — MINOCYCLINE HYDROCHLORIDE (MINOCYCLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0832-2020·2020-02-12

    Graviti Pharmaceuticals Recalls Atorvastatin Calcium Tablets Due to Foreign Tablet Presence

    Graviti Pharmaceuticals is recalling 29,056 bottles of 10 mg Atorvastatin Calcium Tablets because a 20 mg tablet was found in a bottle labeled for 10 mg tablets.

    Product
    Atorvastatin Calcium Tablets, USP, 10 mg*, 90-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ 08830-3009 USA; Manufactured By: Graviti Pharmaceuticals Pvt. Ltd., Telangana -502307, INDIA; NDC 70377-027-11.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0831-2020·2020-02-12

    Teva Recalls Desmopressin Acetate Tablets Due to Missing Desiccant

    Teva Pharmaceuticals USA is recalling Desmopressin Acetate Tablets because bottles may be missing desiccant, a GMP deviation.

    Product
    Desmopressin Acetate Tablets, 0.2 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2465-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0829-2020·2020-02-12

    Unichem Recalls Clonidine Hydrochloride Tablets Due to Benzophenone Migration

    Unichem Pharmaceuticals is recalling Clonidine Hydrochloride tablets due to potential benzophenone migration from container labels. This is a precautionary measure.

    Product
    CLONIDINE HYDROCHLORIDE — CLONIDINE HYDROCHLORIDE (CLONIDINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V074000·2020-02-11

    Blue Bird Recalls 2018-2019 School Buses Due to Wire Harness Defect

    Blue Bird is recalling 2018-2019 Vision and All American school buses because a wire harness connector may unplug, causing sudden loss of drive power and power steering.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V073000·2020-02-10

    Yamaha Recalls 2019 YZF-R3 Motorcycles Due to Brake Hose Holder Defect

    Yamaha is recalling 1,480 2019 YZF-R3 motorcycles because a loose brake hose holder may cause a fluid leak, reducing braking ability and increasing crash risk.

    Product
    YAMAHA — YAMAHA redundant YZFR3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V071000·2020-02-10

    Yamaha Recalls 2019 YZF-R3 Motorcycles Due to Front Brake Hose Chafing

    Yamaha is recalling 1,561 2019 YZF-R3 motorcycles because the front brake hose may chafe against the horn wire, potentially causing a brake fluid leak and reduced braking ability.

    Product
    YAMAHA — YAMAHA redundant YZFR3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V070000·2020-02-10

    Forest River Recalls 2020 Cedar Creek Trailers Due to Fire Risk

    Forest River is recalling 2020 Cedar Creek trailers because the stove may be too close to the window valance, posing a fire hazard.

    Product
    FOREST RIVER — FOREST RIVER CEDAR CREEK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E005000·2020-02-07

    Ferrara Recalls Pelican Flashlights Due to Battery Explosion Risk

    Ferrara Fire Apparatus is recalling Pelican Flashlights models 9410 and 9415 supplied with emergency vehicles because the battery pack may explode while charging.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V068000·2020-02-07

    Mercedes-Benz Recalls 2020 Models for Emergency Call System Location Error

    Mercedes-Benz is recalling 239 vehicles from 2020 because a damaged electrical circuit in the eCall module may relay inaccurate location data, potentially delaying emergency responders.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, E 450, E 350, AMG GT63S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V066000·2020-02-06

    Honda Recalls 2018-2020 Odyssey Vehicles for Electrical Fire Risk

    Honda is recalling 2018-2020 Odyssey vehicles because a pinched wire harness in the third row seat area could cause an electrical short and fire.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V064000·2020-02-06

    Toyota and Lexus Vehicles Recalled Due to Engine Coolant Leak Risk

    Toyota and Lexus vehicles with 2020 model years are recalled because porosity in engine castings may cause coolant leaks, potentially leading to engine overheating, stalling, and fire risk.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4, RAV4 HYBRID, CAMRY HYBRID, CAMRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20069·2020-02-06

    Star Water Systems Recalls Sump Pumps Due to Fire Hazard

    Star Water Systems is recalling about 33,000 sump pumps sold under Utilitech, Do It, and Star Water Systems brands because they can overheat and cause fires.

    Product
    Sump Pumps sold under Utilitech, Do It and Star Water Systems brands
    Category
    Consumer Product
    Distribution
    Distributed nationwide