The Recall Desk

State

US Virgin Islands product recalls

73,570 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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26851–26875 of 73748

  • HighFDA (Devices)·Z-0473-2021·2020-11-25

    Siemens Atellica IM 1300 Analyzer Recalled for Test Definition Scanning Issues

    Siemens Healthcare Diagnostics is recalling Atellica IM 1300 Analyzers because scanning specific test definitions may reset custom settings, causing inaccurate test results.

    Product
    Atellica IM 1300 Analyzer - Product Usage: automated, immunoassay analyzers designed to perform in vitro diagnostic tests on clinical specimens. Siemens Material Number (SMN): 11066001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0451-2021·2020-11-25

    Ortho Recalls VITROS Anti-SARS-CoV-2 IgG Control Due to Signal Issues

    Ortho Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 IgG Control and Calibrator lots due to elevated signal/cutoff values and decreased signal.

    Product
    VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product Usage: For use in monitoring the performance of the VITROS Immunodiagnostic and Integrated Systems when used for the determination of IgG antibodies to SARS-CoV-2. Product Code (Unique Identifier)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0106-2021·2020-11-25

    Apotex Recalls Aripiprazole Tablets Due to Dissolution Failures

    Apotex Corp. is recalling Aripiprazole Tablets 15 mg because they failed to meet dissolution specifications. The affected products were distributed nationwide in the USA.

    Product
    Aripiprazole Tablets, USP 15 mg tablets, packaged in a) 1000 count bottle, NDC 60505-2675-8; b) 30 count bottle, NDC 60505-2675-3; Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0469-2021·2020-11-25

    Siemens Artis X-Ray Systems Recalled for Overvoltage Protection Defect

    Siemens is recalling 26 Artis X-ray systems worldwide because incorrect diodes may fail to protect against overvoltage, potentially causing system malfunction.

    Product
    Artis zee floor, Artis Q ceiling, Artis Q.zen ceiling. Image-Intensified Fluoroscopic X-Ray System. Material numbers 10848281, 10848354, 10094135, 10848354 - Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0101-2021·2020-11-25

    Hikma Recalls Sodium Chloride Injection Vials Due to pH Failures

    Hikma Pharmaceuticals is recalling specific lots of Sodium Chloride Injection USP 0.9% 2 mL vials because they failed pH specifications.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0474-2021·2020-11-25

    Siemens Atellica IM 1600 Analyzer Recalled for Custom Settings Reset

    Siemens Healthcare Diagnostics is recalling Atellica IM 1600 Analyzers because scanning a new kit lot may reset custom settings to defaults.

    Product
    Atellica IM 1600 Analyzer - Product Usage: automated, immunoassay analyzers designed to perform in vitro diagnostic tests on clinical specimens. Siemens Material Number (SMN): 11066000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0450-2021·2020-11-25

    Ortho Recalls VITROS SARS-CoV-2 IgG Calibrators Due to Elevated Signal Values

    Ortho Clinical Diagnostics is recalling specific lots of VITROS SARS-CoV-2 IgG Calibrators because they produced elevated signal values. The recall also includes one lot of IgG Controls with decreased signal.

    Product
    VITROS Immunodiagnostic Products-SARS-CoV-2 IgG Calibrator - Product Usage: In-Vitro Diagnostic (EUA) an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. Emergency use of this test is limited to authorized…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0440-2021·2020-11-25

    Inova Lasers Recalls Class IV New Era Medical Laser Devices

    Inova Lasers LLC is recalling eight Class IV New Era medical laser devices because they failed to comply with Electronic Product Radiation Control regulations.

    Product
    Class IV New Era medical laser device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0458-2021·2020-11-25

    Steris Olympus Leak Test Adapter Recalled for Cleaning Solution Intrusion Risk

    Steris Corporation is recalling Olympus Leak Test Adapters used with Acu-sInQ systems due to a potential for cleaning solution to intrude into endoscopes.

    Product
    Olympus Leak Test Adapter used with Acu-sInQ Complete Endoscope Cleaning Aid Systems-intended to assist manual flexible endoscope cleaning Part number: 0600818OKN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0471-2021·2020-11-25

    Ortho VITROS Chemistry Performance Verifier II Recalled for Product Instability

    Ortho Clinical Diagnostics is recalling VITROS Chemistry Products Performance Verifier II due to product instability that causes biased ALKP values.

    Product
    VITROS Chemistry Products Performance Verifier II-For in vitro diagnostic use only.VITROS Chemistry Products Performance Verifier is an assayed control used to monitor performance on VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and the VITROS 5600/XT 7600 Integrated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0470-2021·2020-11-25

    Micro-Tech Elastic Traction Device Recalled for Regulatory Classification Issues

    Micro-Tech USA is recalling Elastic Traction Devices because they are not appropriately classified as Class I and require 510(k) clearance.

    Product
    Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use in flexible Endoscopy to provide retraction to assist in tissue resection, exposure, and removal of tissue within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V730000·2020-11-24

    Ford Recalls 2020 Explorers Due to Fuel Tank Weld Defect

    Ford is recalling 2020 Explorers with 2.3L engines because an incomplete weld on the fuel tank inlet check valve could cause a fuel leak and fire during a crash.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V729000·2020-11-24

    Mercedes-Benz Metris Recalled for Potential Brake Line Fitting Defects

    Daimler Vans USA is recalling 2019-2020 right-hand drive Mercedes-Benz Metris vehicles because brake line fittings may be incorrectly installed, risking fluid leaks and reduced braking performance.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21710·2020-11-24

    Any Volume Recalls Bicycle Helmets Due to Head Injury Risk

    Any Volume is recalling about 660 adult bicycle helmets sold on eBay because they do not comply with U.S. safety standards, posing a risk of head injury.

    Product
    Bicycle Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20E088000·2020-11-24

    Weldon i4G Vivtech Control Panels Recalled for Electrical Defect

    Weldon is recalling i4G Vivtech control panels because an electrical defect may cause the display to stop working, potentially delaying emergency services.

    Product
    ELECTRICAL SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V727000·2020-11-23

    Multiple recreational vehicle models recalled for cooking stove gas leak

    Forest River and Coachmen recreational vehicles with Dometic 3-burner cooking stoves may experience gas leaks from overtightened saddle valve bolts, creating a fire hazard. Owners should contact dealers for a free remedy kit.

    Product
    COACHMEN — COACHMEN, FOREST RIVER, DYNAMAX CROSS TREK, FREELANDER, LEPRECHAUN, MIRADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V728000·2020-11-23

    Rosenbauer Aerial Vehicles Recalled for Power Take-Off Defect

    Rosenbauer America is recalling 2018-2020 Aerial vehicles because the power take-off may disengage, causing the aerial device to become inoperable.

    Product
    ROSENBAUER — ROSENBAUER AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V721000·2020-11-20

    Isuzu and Chevrolet Recall 2020 Trucks for Wiring Chafe Risk

    Isuzu and Chevrolet are recalling 2020 NPR-HD and 4500 Crew Cab trucks because a chafing wire harness or hose could cause a short circuit, engine stall, or fire.

    Product
    ISUZU — ISUZU, CHEVROLET NPR HD, LOW CAB FORWARD 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V720000·2020-11-20

    Isuzu and Chevrolet Trucks Recalled for Battery Cable Fire Risk

    Isuzu and Chevrolet are recalling 2020 NPR-HD and 4500 trucks because a battery cable may overheat near the exhaust, posing a fire risk.

    Product
    ISUZU — ISUZU, CHEVROLET NPR HD, LOW CAB FORWARD 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide