The Recall Desk

State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42426–42450 of 73919

  • HighFDA (Devices)·Z-2714-2017·2017-07-19

    ArjoHuntleigh Flowtron ACS900 Medical Pump Recalled for Deflation Failure

    Arjo, Inc. is recalling 40,675 Flowtron ACS900 medical pumps worldwide because the device may fail to deflate the calf garment as intended without triggering an alarm.

    Product
    ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein Thrombosis (DVT) in at-risk patients. The system must be used as part of a prescribed plan of car under the supervision of trained medical and/or Clinical staff.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2588-2017·2017-07-19

    NatureBox Mini Crispy Snickerdoodles Recalled for Cashew Fragment

    NatureBox is recalling Mini Crispy Snickerdoodles because a cashew fragment was found during packing, posing a potential allergen risk.

    Product
    NatureBox Mini Crispy Snickerdoodles: Cinnamon-sugar cookies made with whole wheat. Contains: Wheat, Milk and Egg.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2463-2017·2017-07-19

    3CS Organics Recalls HIPP Infant Formula Due to Labeling Issues

    3CS Organics LLC is recalling HIPP infant formula products because they are not FDA approved and lack full English labeling.

    Product
    HIPP HA Combiotik HA 1, 500g (4/case), HIPP Combiotik HA 2, 500g (4/case), HA Combiotik Pre HA, 500g (4/case), HIPP Combiotic Growing Up Milk 3, 600g (4bx/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2711-2017·2017-07-19

    Toshiba APLIO 500 Ultrasound Systems Recalled for Incorrect Velocity Trace Values

    Toshiba American Medical Systems Inc. is recalling 307 APLIO 500 diagnostic ultrasound systems because they may display incorrect values when using the Continuous Trace method on Spectral Doppler.

    Product
    APLIO 500 TUS-A500 diagnostic ultrasound system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2380-2017·2017-07-19

    Source Naturals Hydrogen Boost Capsules Recalled for Undeclared Boron

    Source Naturals Hydrogen Boost Capsules are being recalled because they contain low levels of undeclared boron. The recall covers 55,354 units distributed nationwide.

    Product
    Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1855: 60 count Bottle - Product SN1856; 6 count Bottle - Product SN2314; 30 count + 30…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2464-2017·2017-07-19

    3CS Organics Recalls HIPP Organic Infant Milk Products for Labeling Issues

    3CS Organics is recalling HIPP Organic infant milk products because they are not FDA approved and lack full English labeling.

    Product
    HIPP Organic Comb Hungry Infant Milk, 800g (4bx/case), HIPP Organic Comb First Infant Milk, 800g (4bx/case), HIPP Organic Combiotic Follow on Milk 2, 800g (4bx/case), HIPP Organic Good Night Milk from 6 Months, 350g (12cans/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2465-2017·2017-07-19

    HIPP Infant Formula Recalled for Lack of FDA Approval and English Labels

    3CS Organics LLC is recalling HIPP infant formula products because they are not FDA approved and lack complete English labeling.

    Product
    HIPP Tetrapack-Liquid , Single Serve Combiotik Hungry Infant, 200mL (6pk/24cases), HIPP Tetrapak-Liquid, Single Serve Combiotik First Infant Milk, 200mL (6pk/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2708-2017·2017-07-19

    Toshiba XARIO 100 Ultrasound Systems Recalled for Incorrect Velocity Readings

    Toshiba American Medical Systems is recalling seven XARIO 100 diagnostic ultrasound systems because they may display incorrect values when using the Continuous Trace method for velocity measurements.

    Product
    XARIO 100 TUS-X100 diagnostic ultrasound system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2469-2017·2017-07-19

    3CS Organics Recalls Topfer Lactana Bio Infant Formula for Labeling Issues

    3CS Organics LLC is recalling Topfer Lactana Bio infant and follow-up formula because the product is not FDA approved and lacks complete English labeling.

    Product
    Topfer Lactana Bio 1 Anfangsmilch, 600g (3/case), Topfer Lactana Bio 2, Bio Folgemilch, 600g (3bx/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2462-2017·2017-07-19

    3CS Organics Recalls HIPP Bio Combiotik Infant Formula for Labeling Issues

    3CS Organics LLC is recalling HIPP Bio Combiotik infant formula products because they are not FDA approved and not all products are labeled in English.

    Product
    HIPP Bio Combiotik 1, Canister, 900g (4/case), HIPP Bio Combiotik 2, Canister, 900g (4/case), HIPP Bio Combiotik 3, Canister, 900g (4/case), HIPP Bio Combiotik 1, 600g (4bx/case), HIPP Bio Combiotik 2, 600g (4bx/case), HIPP Bio Combiotik 3, 600g (4/case), HIPP Bio Compiotik…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2467-2017·2017-07-19

    HOLLE Organic Infant Formula Recalled for Lack of FDA Approval

    3CS Organics LLC is recalling HOLLE organic infant formula products because they are not FDA approved and lack English labeling.

    Product
    HOLLE Bio Zulgelingen Opvolgmelk 2, (3/case), HOLLE Bio Lait de suite, 2, 400g (6/case), HOLLE Bio Lait pour Nourrissons Zulgelingenmelk, 400g (6/case), HOLLE Lait Pour Nourrissons 1er Age Bio, 400g (6/case). HOLLE Bio Lait de Suit Au Lait De Chevre, 400g (6/case) , HOLLE…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2730-2017·2017-07-19

    Beckman Coulter Synchron AQUA CAL Level 1 Calibration Kits Recalled

    Beckman Coulter is recalling Synchron AQUA CAL Level 1 kits due to a sodium recovery shift that may affect system calibration.

    Product
    Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl, Urea N, Urea, Glucose Creatine, Ca, CO2, and P in UniCel DxC Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2383-2017·2017-07-19

    Source Naturals Renewal Antioxidant Tablets Recalled for Undeclared Boron

    Threshold Enterprises Ltd is recalling Source Naturals Renewal Antioxidant Tablets because they contain low levels of undeclared boron.

    Product
    Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack, 30 Count, 60 Count, & 120 Count per bottle; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1750: 60 count Bottle - Product SN1751; 120 count…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2461-2017·2017-07-19

    HIPP Anti-Reflux Infant Formula Recalled for Lack of FDA Approval

    3CS ORGANICS LLC is recalling HIPP Anti-Reflux AR Bio-Spezialnahrung because the product is not FDA approved and lacks complete English labeling.

    Product
    HIPP Anti-Reflux AR Bio-Spezialnahrung, 500g (4/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2715-2017·2017-07-19

    CryoLife On-X Prosthetic Heart Valve Recall for Incorrect Labeling

    CryoLife, Inc. is recalling 52 On-X Prosthetic Heart Valves because the sewing ring type was mislabeled as Standard instead of Anatomic.

    Product
    On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic heart valves in the aortic and mitral positions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2701-2017·2017-07-19

    Natus Medical Recalls Olympic Pasteurmatic 3000 and 3500 Disinfection Systems

    Natus Medical is recalling Olympic Pasteurmatic 3000 and 3500 systems because they do not fully meet current regulatory requirements due to design age and component obsolescence.

    Product
    The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of respiratory therapy and anesthesia equipment by killing vegetative bacteria and viruses, in a hot water bath at ~160¿ - ~170¿ F for 30 minutes. Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2468-2017·2017-07-19

    3CS Organics Recalls Lebenswert Infant and Toddler Milk Formulas

    3CS Organics LLC is recalling specific Lebenswert infant and toddler milk formulas because the products are not FDA approved and lack full English labeling.

    Product
    Lebenswert Bioland Anfangsmilch1, 500g (4/case), Lebenswert Bioland Folgemilch 2, 500g (4/case), Lebenswert Bioland Folgemilch 3, 475g (5/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2725-2017·2017-07-19

    AMS Diagnostics Recalls Medica ISE Module Calibrant A Due to Physical Defects

    AMS Diagnostics is recalling 9 units of Medica ISE Module Calibrant A because the lot was not functioning properly and did not exhibit correct physical properties.

    Product
    Medica ISE Module Calibrant A; 500 mL - 140 mmol/L Na+, 125 mmol/L Cl-, buffers and preservatives; For use with ISE Module; Product Usage: Calibrations of ISE Model for integrated electrolyte system analysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V457000·2017-07-18

    Mazda Recalls CX-7, CX-9, and Mazda6 for Air Bag Inflator Rupture Risk

    Mazda is recalling specific 2007-2012 CX-7, CX-9, and Mazda6 vehicles because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA CX-9, CX-7, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E038000·2017-07-18

    TriMark Recalls Ambulance Door Striker Bolts for Crash Safety Non-Compliance

    TriMark is recalling specific door striker bolts used in ambulance door systems because they may fail during a crash, causing doors to open and increasing injury risk.

    Product
    STRUCTURE:BODY:DOOR:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17756·2017-07-18

    Polaris Recalls RZR 570 and RZR S 570 Off-Highway Vehicles

    Polaris is recalling about 1,160 RZR 570 and RZR S 570 vehicles because the front brake can detach, posing crash and injury hazards.

    Product
    Polaris RZR 570 and RZR S 570 recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V456000·2017-07-18

    Winnebago Recalls 2015 Transit Buses for Weight Rating Compliance Issues

    Winnebago is recalling 2015 Transit Bus 28SH and 28WC models because they may exceed weight ratings when fully loaded, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO TRANSIT BUS28SH, TRANSIT BUS28WC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V455000·2017-07-18

    Pierce Fire Trucks Recalled for Water Pump Interlock Failure

    Pierce is recalling 2016-2017 fire trucks because a pressure switch may fail in extreme cold, preventing the water pump from operating.

    Product
    PIERCE — PIERCE ENFORCER, VELOCITY, QUANTUM, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide