The Recall Desk

State

US Virgin Islands product recalls

73,219 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
30
Most recent
2026-09-23

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 30 (17%) are Severe.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18251–18275 of 73396

  • SevereCPSC·23034·2022-11-03

    BLACK+DECKER Garment Steamers Recalled for Burn Hazard from Hot Water

    Empower Brands recalls about 518,500 BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, posing a burn hazard. The company has received 241 reports of hot water expelling, including 32 reports of burn injuries.

    Product
    BLACK+DECKER Model HGS011 Easy Garment Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23032·2022-11-03

    FUUL Lamp Oil Recalled for Non-Child-Resistant Packaging and Labeling Failures

    FHS Retail is recalling about 1,700 units of FUUL 1.9L Pure Liquid Paraffin Lamp Oil because the packaging is not child-resistant and the label omits mandatory safety information required by federal law. The product can cause fatal chemical pneumonia or lung damage if ingested.

    Product
    FUUL 1.9L Pure Liquid Paraffin Lamp Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V825000·2022-11-03

    2021-2022 Ford Bronco Rearview Camera Display May Distract Drivers

    Ford is recalling 2021-2022 Bronco vehicles with rearview camera systems because the camera image may remain displayed after the vehicle shifts out of reverse, potentially distracting drivers and increasing crash risk.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23035·2022-11-03

    AirWick Fresh New Day Aerosol Air Fresheners Recalled for Rupture and Laceration Risk

    Reckitt is recalling about 67,000 AirWick Fresh New Day aerosol air fresheners in Fresh Linen and Fresh Waters scents due to a missing corrosion inhibitor in one batch that can cause cans to rupture or leak. No injuries have been reported.

    Product
    AirWick Fresh New Day® aerosol air fresheners - "Fresh Linen" and "Fresh Waters" scents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23036·2022-11-03

    Clarks Women's Navy Canvas Shoes Recalled for Chemical Hazard

    Clarks Americas is recalling three styles of women's navy canvas shoes sold from February to October 2022 because prolonged contact with the shoe material can expose wearers to toxic chemicals benzidine and/or dimethoxybenzidine.

    Product
    Breeze Ave, Breeze Shore and Breeze Step women's shoes in navy colors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V827000·2022-11-03

    2021 Cadillac Escalade daytime running lights control software defect

    General Motors is recalling 2021 Cadillac Escalade vehicles. The daytime running lights may not deactivate when headlights are on, which may cause glare and reduce visibility, increasing crash risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SUBURBAN, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23707·2022-11-03

    BS Interactive Stashables Finger Skateboard Ramp Sets Lead Paint Hazard

    BS Interactive is recalling Stashables Finger Skateboard Ramp Sets because the miniature skateboards and scooters contain lead paint levels exceeding federal limits and fail lead content bans, posing a lead poisoning risk to young children.

    Product
    Stashables Finger Skateboard Ramp Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23708·2022-11-03

    Myx Connected Exercise Bicycles Recalled for Pedal Detachment Risk

    Myx is recalling approximately 162,000 MYX I, MYX II, and MYX II Plus exercise bicycles because pedals can loosen or detach during use, causing injury. Myx has received 864 reports of pedal loosening or detachment, including 75 injury reports involving bruises and cuts.

    Product
    MYX I, MYX II and MYX II Plus Connected Exercise Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23031·2022-11-03

    Bolt Foldable Children's Scooters Recalled for Excessive Lead Paint

    Anker Play Products is recalling about 5,000 Bolt Foldable Children's Scooters sold at discount stores from March through May 2022. The paint contains lead levels exceeding the federal ban, creating a lead poisoning hazard for young children.

    Product
    Bolt Foldable Children's Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V826000·2022-11-03

    Micro Bird Recalls School Buses Due to Incorrectly Attached Rub Rails

    Micro Bird is recalling 2021-2023 G5, 2022-2023 MB II, and 2022 T-Series school buses because seat-level rub rails may be incorrectly attached, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, MB II SCHOOL BUS, T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23033·2022-11-03

    Tangame Busy Toy Houses Recalled for Lead Paint and Phthalate Violations

    Tangame Busy Houses, wooden activity toy cubes sold on Amazon, contain lead paint on a zipper, lead in a plastic phone cord, and phthalates in a horn bulb, exceeding federal safety bans. No injuries have been reported.

    Product
    Tangame Busy Houses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23709·2022-11-03

    Rad Power Bikes RadWagon 4 Electric Cargo Bikes Recall

    Rad Power Bikes is recalling about 29,300 RadWagon 4 electric cargo bikes because the tires can unexpectedly go flat or separate, risking falls and crashes. The firm has received 137 reports of tire failures and eight injury reports.

    Product
    RadWagon 4 Electric Cargo Bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0019-2023·2022-11-02

    Atenolol 25mg bottles mislabeled; contain Clopidogrel 75mg tablets

    Golden State Medical Supply Inc. is recalling 2,584 bottles of Atenolol 25mg tablets nationwide. Bottles labeled as Atenolol 25mg actually contain Clopidogrel 75mg tablets—a different medication.

    Product
    ATENOLOL — ATENOLOL (ATENOLOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0023-2023·2022-11-02

    Sodium Bicarbonate Injection Recalled for Defective Vials and Glass Breakage

    Nationwide recall of 8.4% sodium bicarbonate injection vials due to container defects causing vial breakage and glass fragments when pressurized during preparation.

    Product
    8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, Inc. Lehi, Utah 84043, Mfd by: Exela Pharma Sciences, LLC, Lenoir, NC 28645, Carton NDC 72572-740-20, vial NDC 72572-740-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V824000·2022-11-02

    Quality Trailers Ohio Recalls 2022 Trailers Due to Coupler Welding Defect

    Quality Trailers Ohio is recalling 2022 A, AW, B, and DH trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle.

    Product
    QUALITY TRAILERS OHIO — QUALITY TRAILERS OHIO TANDEM B, ECONOMY SERIES DH, AW, A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0022-2023·2022-11-02

    Sodium Bicarbonate Injection Recalled for Defective Vials with Glass Breakage Risk

    Exela Pharma Sciences is recalling 2,123,040 vials of Sodium Bicarbonate 8.4% Injection due to container defects causing vial breakage and glass release when pressurized during product preparation.

    Product
    SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0124-2023·2022-11-02

    Medline Pre-Op CHG Bathing Kit recalled for incorrect expiration dates

    Medline is recalling 460 Pre-Op CHG Bathing Kits because the CHG solution and blood culture bottles have expiration dates that don't match the kit label. Expired components could compromise effectiveness.

    Product
    MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V823000·2022-11-02

    2022 Audi and Volkswagen vehicles recalled for blank rearview cameras

    Certain 2022 Audi and Volkswagen vehicles have a defective rearview camera that may go blank or unresponsive, reducing rear visibility. Dealers will replace the camera for free.

    Product
    AUDI — AUDI, VOLKSWAGEN RS 3, GTI, ID.4, Q4 E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0122-2023·2022-11-02

    Medline Blood Culture Kits recalled due to mismatched component expiration dates

    Medline Industries is recalling 1,600 blood culture kits (Reorder # DYNDH1592) because component expiration dates don't match the kit label. Affected components include CHG Solution and Bactec bottle plastic.

    Product
    MEDLINE BLOOD CLUTURE KIT, Reorder #: DYNDH1592
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0119-2023·2022-11-02

    ARTIS pheno interventional x-ray system software defect prevents treatment continuation

    Siemens is recalling ARTIS pheno x-ray systems with VE10B software due to three potential software issues that may prevent continued treatment on the affected system, potentially requiring use of an alternate system.

    Product
    ARTIS pheno, Interventional fluoroscopic x-ray system, Model No. 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0140-2023·2022-11-02

    Stryker INBONE Tibial Tray recalled for oversized lock detail defect

    Wright Medical Technology is recalling one Stryker INBONE Tibial Tray due to an oversized tibial tray lock detail that exceeds product specifications and could affect device functionality.

    Product
    Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 18mm Stem Base, REF 200252904, Size 4
    Category
    Medical Device
    Distribution
    Distributed nationwide