The Recall Desk

State

US Virgin Islands product recalls

73,734 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33976–34000 of 73912

  • HighFDA (Devices)·Z-1304-2019·2019-05-15

    ConMed Anchor Tissue Retrieval System Recalled for Seal Defects

    ConMed is recalling Anchor Tissue Retrieval Systems because voids or partial seals may compromise sterility. The recall covers units distributed worldwide.

    Product
    ConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: TRS100SB2 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1306-2019·2019-05-15

    ConMed Anchor Tissue Retrieval System Recalled for Sterility Seal Defects

    ConMed is recalling Anchor Tissue Retrieval Systems due to seal defects that may compromise sterility. The recall covers 5,034 units distributed worldwide.

    Product
    ConMed Anchor Tissue Retrieval System, 15 MM, 1850 ML (3/BX) Catalog Number:TRS190SB2 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1303-2019·2019-05-15

    Zimmer Biomet Recalls T7 Driver Solid AO Due to Fracture Risk

    Zimmer Biomet is recalling 1,924 T7 Driver Solid AO units because they may fracture, bend, or shear during use.

    Product
    T7 Driver Solid AO (Part Number 110018541) Product Usage: The Biomet Headless Compression Screws and Twist-Off Screws are indicated for fixation of bone fractures, fusion of a joint (arthrodesis) or bone reconstruction (osteotomy) of the mid-foot bones, metatarsal and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1285-2019·2019-05-15

    Cardinal Health Recalls ChemoPlus Goggles Due to Latex Mislabeling

    Cardinal Health is recalling ChemoPlus Protective Wrap-around Goggles because the kit labels state they are latex-free, but the goggle straps contain natural rubber latex.

    Product
    ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1286-2019·2019-05-15

    Cardinal Health Recalls ChemoPlus Chemo Spill Kits Due to Latex

    Cardinal Health 200, LLC is recalling ChemoPlus Chemo Spill Kits because the safety goggles inside contain natural rubber latex, despite the kit label stating the product is latex-free.

    Product
    ChemoPlus Chemo Spill Kit, Home Health Kit Product Code:DP5108K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19122·2019-05-15

    Beaba Recalls Babycook Neo Steam Cookers Due to Glass Bowl Laceration Hazard

    Beaba is recalling Babycook Neo steam cooker/blenders because the glass bowl can shatter, posing a laceration hazard. Consumers should stop using the product and contact Beaba for a free replacement.

    Product
    Babycook Neo steam cooker/blenders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1305-2019·2019-05-15

    ConMed Anchor Tissue Retrieval System Recalled for Seal Defects

    ConMed is recalling Anchor Tissue Retrieval Systems because voids or partial seals may compromise the sterility of the product.

    Product
    ConMed Anchor Tissue Retrieval System 15 MM, 1550 ML (3/BX) Catalog Number: TRS175SB2 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1307-2019·2019-05-15

    ConMed Anchor Tissue Retrieval System Recalled for Seal Defects

    Conmed Corporation is recalling the Anchor Tissue Retrieval System due to seal defects that may compromise sterility.

    Product
    ConMed Anchor Tissue Retrieval System, VATS, 15 MM, 1550 ML (3/BX) Catalog Number: TRS-VATS-15 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1298-2019·2019-05-15

    Siemens Cios Alpha Mobile X-ray System Recalled for Component Wear

    Siemens is recalling 257 Cios Alpha mobile X-ray systems because continuous high-output use may cause premature failure of radiation components.

    Product
    Cios Alpha, Model Number 10308191 Mobile X-ray system - Product Usage: The Cios Alpha is a mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications. Clinical applications may include but are not limited to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1283-2019·2019-05-15

    Cardinal Health Recalls ChemoPlus Spill Kits Due to Latex Mismatch

    Cardinal Health is recalling ChemoPlus chemotherapy spill kits because the safety goggles inside contain natural rubber latex, despite the kit label stating the product is latex-free.

    Product
    ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1289-2019·2019-05-15

    Ortho-Clinical VITROS 3600 Immunoassay System Software Recall

    Ortho-Clinical Diagnostics is recalling VITROS 3600 Immunoassay System software versions 3.3.2 and below due to a luminometer malfunction that may prevent the processing of MicroWell assays.

    Product
    VITROS¿ 3600 Immunoassay System-Software V3.3.2 & below Product Code: 6802783 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1288-2019·2019-05-15

    Ortho-Clinical VITROS 5600 Systems Recalled for Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems due to a luminometer malfunction that may prevent the processing of MicroWell assays.

    Product
    VITROS¿ 5600 Integrated System Refurbished-Software V3.3.2 & below Product Code: 6802915 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1294-2019·2019-05-15

    Medica Wash1 Solution Recalled for Ineffective Probe Cleaning

    Medica Corporation is recalling Wash1 solution because it fails to clean the probe effectively, potentially causing test interference on the EasyRA analyzer.

    Product
    Medica Wash1-Wash solution used prior to Lipase assay on the EasyRA clinical chemistry analyzer REF 10680 - Product Usage: For use in washing the probe of the Medica EasyRA Chemistry Analyzer. The wash solution in the wedge is used to prevent interference between certain…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1291-2019·2019-05-15

    Ortho-Clinical Diagnostics Recalls VITROS XT 7600 Systems Due to Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling 62 VITROS XT 7600 Integrated Systems worldwide because a luminometer malfunction may prevent the processing of MicroWell assays.

    Product
    VITROS¿ XT 7600 Integrated System-Software V3.4.1 & below Product Code: 6844461 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1284-2019·2019-05-15

    Cardinal Health Recalls ChemoPlus Spill Kits Due to Latex Inconsistency

    Cardinal Health is recalling ChemoPlus chemotherapy spill kits because the safety goggles inside contain natural rubber latex, despite the kit label stating the product is latex-free.

    Product
    ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1293-2019·2019-05-15

    Ortho-Clinical VITROS ECi Immunodiagnostic System Recalled for Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling 25 refurbished VITROS ECi Immunodiagnostic Systems because a luminometer malfunction may prevent the processing of MicroWell assays.

    Product
    VITROS ECi Immunodiagnostic System Refurbished Product Code: 6801059 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1297-2019·2019-05-15

    Elekta Unity Systems Recalled for Missing Contrast Agent Warnings

    Elekta Limited is recalling nine Elekta Unity systems because the user manual lacks a warning regarding the administration of unvalidated contrast agents.

    Product
    Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance Imaging is indicated for radiation therapy treatments and stereotactic radiation treatments of malignant and benign diseases anywhere in the body as determined by a licensed medical practitioner in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1292-2019·2019-05-15

    Ortho-Clinical VITROS ECi/ECiQ Immunodiagnostic System Recalled for Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling 45 VITROS ECi/ECiQ Immunodiagnostic Systems worldwide due to a luminometer malfunction that may prevent the processing of MicroWell assays.

    Product
    VITROS¿ ECi/ECiQ Immunodiagnostic System Product Code: 1922814 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1290-2019·2019-05-15

    Ortho-Clinical Diagnostics Recalls VITROS 3600 Immunoassay Systems Due to Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling 28 VITROS 3600 Immunoassay Systems because a luminometer malfunction may prevent the processing of MicroWell assays.

    Product
    VITROS¿ 3600 Immunoassay System Refurbished-Software V3.3.2 & below Product Code: 6802914 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1287-2019·2019-05-15

    Ortho-Clinical Diagnostics Recalls VITROS 5600 Integrated System Software

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated System software versions 3.3.2 and below due to a luminometer malfunction that may prevent the processing of MicroWell assays.

    Product
    VITROS¿ 5600 Integrated System -Software V3.3.2 & below Product Code: 6802413 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V367000·2019-05-14

    Daimler Trucks Recalls 2019 Freightliner and Western Star Trucks for Brake Bolt Issue

    Daimler Trucks North America is recalling 253 specific 2019 heavy-duty trucks because brake caliper mounting bolts may be insufficiently tightened, potentially reducing brake effectiveness.

    Product
    FCCC — FCCC, FREIGHTLINER, WESTERN STAR XCL, XCS, CASCADIA, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V368000·2019-05-14

    2019 Thomas Built Buses Saf-T-Liner C2 Brake Recall

    Daimler Trucks North America is recalling 2019 Thomas Built Buses Saf-T-Liner C2 vehicles because loose brake caliper bolts may reduce braking effectiveness.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V370000·2019-05-14

    Daimler Trucks Recalls 741 Vehicles for Insufficient Brake Air Reservoir Capacity

    Daimler Trucks North America is recalling 741 Freightliner, Sterling, and Western Star trucks because insufficient air reservoir capacity may reduce brake effectiveness and increase crash risk.

    Product
    STERLING — STERLING, FREIGHTLINER, WESTERN STAR ACTERRA, LT9500, L8500, CLASSIC XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V371000·2019-05-14

    Daimler Trucks Recalls MT55 and MT45 Chassis for Brake Pedal Defect

    Daimler Trucks North America is recalling 2012-2019 Freightliner Custom Chassis MT55 and MT45 vehicles because a brake pedal clip may detach, causing brake light failure or pedal detachment.

    Product
    FCCC — FCCC MT55, MT45
    Category
    Vehicle
    Distribution
    Distributed nationwide