The Recall Desk

State

US Virgin Islands product recalls

73,509 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
39
Most recent
2026-10-14

Of the 177 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.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25751–25775 of 73686

  • HighCPSC·21089·2021-02-25

    Dr. Reddy's Recalls Prescription Blister Packages Due to Poisoning Risk

    Dr. Reddy's is recalling prescription blister packages because the packaging is not child-resistant, posing a poisoning risk to young children.

    Product
    Imatinib Mesylate Tablets 100 mg, Imatinib Mesylate Tablets 400 mg, Pregabalin Capsules 50 mg, Pregabalin Capsules 75 mg, Pregabalin Capsules 100 mg, Pregabalin Capsules 150 mg, Sevelamer Carbonate Tablets 800 mg, Tadalafil Tablets 5 mg and Tadalafil Tablets 20 mg
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·21722·2021-02-25

    Home Depot Recalls Wood Windsor Dining Chair Sets Due to Fall Hazard

    Home Depot is recalling StyleWell Wood Windsor Dining Chair Sets because the back can detach, posing a fall hazard. No injuries have been reported.

    Product
    StyleWell Wood Windsor Dining Chair Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V117000·2021-02-25

    Land Rover Recalls 2018-2020 Models for High Beam Indicator Defect

    Jaguar Land Rover is recalling 2018-2020 Range Rover and Discovery models because the high beam indicator may not display, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT, RANGE ROVER VELAR, DISCOVERY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V116000·2021-02-25

    Black Series Campers Recalls Trailers Due to Electrical Fire Risk

    Black Series Campers is recalling 2020-2021 trailers equipped with specific Curt emergency breakaway kits because a depleted battery can overload the electrical system, increasing the risk of a fire.

    Product
    BLACK SERIES CAMPERS — BLACK SERIES CAMPERS HQ21, HQ19T, HQ19, C12
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21723·2021-02-25

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

    MTIG Productions is recalling deSensua Wintergreen, Birch, and Pain Soother Essential Oils because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.

    Product
    deSensua Wintergreen, Birch and Pain Soother Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0255-2021·2021-02-24

    Optimus Lubricants Hand Sanitizer Recalled for Methanol Contamination

    Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

    Product
    OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 1 Gal (3.78 L) bottle, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477; NDC: XXXXX-378-04, UPC # 7 501799 118837
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0253-2021·2021-02-24

    Optimus Lubricants Hand Sanitizer Recalled for Methanol Contamination

    Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

    Product
    OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 8.5 Fl. Oz. (250 mL) bottle, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477. UPC # 7 501799 115621
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0256-2021·2021-02-24

    Optimus Lubricants Instant Hand Sanitizer Recalled for Methanol Contamination

    Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

    Product
    OPTIMUS LUBRICANTS Instant Hand Sanitizer, (alcohol 70% v/v) 275 Gal (1040 L) tank with spout dispenser, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477.; UPC # 7 501799 118981
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0254-2021·2021-02-24

    Liq-E Recalls Optimus Hand Sanitizer Due to Methanol Contamination

    Liq-E S.A. De C.V. is recalling 575 drums of Optimus Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

    Product
    OPTIMUS LUBRICANTS Instant Hand Sanitizer, (alcohol 70% v/v) 55 Gal (208 L) drum, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col.. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477.UPC # 7 501799 118998
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1114-2021·2021-02-24

    Combat Medical Systems Recalls Fresh Whole Blood Donor Sets

    Combat Medical Systems is recalling 954 Fresh Whole Blood Donor Sets due to a potential bent or disconnected needle in the kit components.

    Product
    Fresh Whole Blood Donor Set (P/N 80-801-D NSN 6515016640306) . Blood convenience kit. The Fresh Whole Blood Doner Set contains everything needed to test for ABO/Rh compatibility and collect the whole blood from donor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V107000·2021-02-24

    Lamborghini Recalls Aventador SVJ Vehicles Due to Hood Hinge Defect

    Lamborghini is recalling 2018-2021 Aventador SVJ vehicles because hood hinge screws may loosen, potentially causing the hood to detach at high speeds.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1113-2021·2021-02-24

    Combat Medical Systems Recalls Fresh Whole Blood Transfusion Sets

    Combat Medical Systems is recalling Fresh Whole Blood Transfusion Sets due to a potential for bent or disconnected needles in the kit components.

    Product
    Fresh Whole Blood Transfusion Set (P/N 80-801 NSN 6515016574750) . Blood convenience kit. The Fresh Whole Blood Transfusion Set contains everything needed to test for ABO/Rh compatibility and perform a fresh whole blood transfusion in a compact sealed package.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1112-2021·2021-02-24

    Combat Medical Systems Recalls Low Titer Type O FWB Transfusion Sets

    Combat Medical Systems, LLC is recalling 1021 units of Low Titer Type O FWB Transfusion Sets due to the potential for bent or disconnected needles in the components.

    Product
    Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN 651501684994). Blood convenience kit. The Transfusion Set includes the items necessary to administer the collected blood to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1110-2021·2021-02-24

    Combat Medical Systems Recalls Valkyrie LTOWB Blood Collection Kits

    Combat Medical Systems is recalling 531 Valkyrie LTOWB blood collection kits due to a potential for bent or disconnected needles.

    Product
    Valkyrie LTOWB Collection (P/N 80-820, NSN 6515016862423). Blood collection convenience kit. The Valkyrie LTOWB Collection Set includes the items needed to allow for pre-screening to identify Low Titer Type O Donors as well as collect the blood from the donor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1111-2021·2021-02-24

    Combat Medical Systems Recalls Valkyrie LTOWB Blood Administration Kits

    Combat Medical Systems is recalling 953 Valkyrie LTOWB Administration Sets due to a potential for bent or disconnected needles.

    Product
    Valkyrie LTOWB Administration (P/N 80-821 NSN 6515016862401). Blood convenience kit. The Valkyrie LTOWB Administration Set contains the items needed to administer the blood to the patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V112000·2021-02-24

    2021 International LT Trucks Recalled for Potential Flywheel Detachment

    Certain 2021 International LT vehicles with Cummins X15 engines may have improperly torqued flywheel capscrews that could detach during operation, causing loss of drive power and risk of ejected engine parts.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1109-2021·2021-02-24

    BD 10 ml Syringes Recalled for Potential Open Seals and Sterility Compromise

    Becton Dickinson is recalling 155,200 10 ml syringes because open packaging seals may compromise sterility. The product was distributed in the US and Canada.

    Product
    BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1126-2021·2021-02-24

    Confirm Biosciences Recalls Orient Gene COVID-19 Rapid Test Cassettes

    Confirm Biosciences is recalling Orient Gene COVID-19 Rapid Test Cassettes because they were distributed outside Emergency Use Authorization and not validated for fingerstick use.

    Product
    Orient Gene COVID- 19 IgG/ IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCCOV-402a - Product Usage: is a lateral flow immunoassay intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV- 2 in human venous whole blood, plasma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21087·2021-02-24

    Urban Outfitters Recalls Margo Taper Candle Holders Due to Fire Hazard

    Urban Outfitters is recalling Margo Taper Candle Holders because they can catch fire if they contact the flame. One fire incident was reported, with no injuries.

    Product
    Margo Taper Candle Holders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1124-2021·2021-02-24

    Getinge CM320 Washer Disinfector Recalled for Hose Deformation Risk

    Getinge is recalling CM320 Series Washer Disinfectors because plastic inlet hose connections may deform or break, potentially causing water leaks and burns.

    Product
    Getinge CM320 Series Washer Disinfector - Product Usage: A multi chamber washer disinfector intended for washing, disinfecting and drying of surgical instruments, containers, operating theatre shoes and operating theatre accessories normally used in hospitals and central…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1131-2021·2021-02-24

    Biomet Recalls Mislabelled 25mm Shoulder Prosthesis Central Screws

    Biomet is recalling 49 units of 25mm central screws for shoulder prostheses because they were mislabeled as 25mm but are actually 40mm.

    Product
    Central Screw 6.5x25mm - Product Usage: used as a sterile screw that is intended for implantable shoulder prosthesis assembly and/or fixation.
    Category
    Medical Device
    Distribution
    Distributed nationwide