The Recall Desk

State

US Virgin Islands product recalls

73,218 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 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17001–17025 of 73395

  • HighNHTSA·23V113000·2023-02-23

    2015–2023 Thor Motor Coach Palazzo Front Brackets May Detach While Driving

    Thor Motor Coach is recalling 1,969 Palazzo recreational vehicles from model years 2015–2023 because front brackets supporting the fiberglass panel may become loose and detach while driving, creating a road hazard.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH PALAZZO, redundant PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23130·2023-02-23

    Two Million Cosori Air Fryers Recalled for Fire and Burn Hazards

    Atekcity Corporation is recalling about 2 million Cosori air fryers because a wire connection can overheat, posing fire and burn hazards. The firm has received 205 reports of fires, with 10 minor burn injuries and 23 reports of minor property damage.

    Product
    Cosori Air Fryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V115000·2023-02-23

    2021-2023 Dodge Durango Recalled for Misaligned Rear Spoiler Detachment Risk

    Chrysler is recalling 2021-2023 Dodge Durango vehicles because the rear spoiler may not be properly aligned with the roof. The misaligned spoiler can be damaged during liftgate use and potentially detach, becoming a road hazard.

    Product
    DODGE — DODGE DURANGO, DURANGO1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V119000·2023-02-23

    International commercial trucks recalled for park brake software defect

    Navistar is recalling 2018-2022 International trucks with a software defect that may prevent the park brake from holding during power-take-off operation, risking unexpected vehicle movement.

    Product
    INTERNATIONAL — INTERNATIONAL MV, HV, RH, HX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23132·2023-02-23

    Zinus SmartBase Euro Slats Metal Platform Bed Frames Recalled for Collapse Hazard

    Zinus is recalling about 30,400 SmartBase Euro Slats metal platform bed frames because missing reinforcing brackets can cause the frame to collapse, creating an injury hazard. Consumers should stop using the bed frames and request a free repair kit.

    Product
    SmartBase® Euro Slats Metal Platform Bed Frames
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23129·2023-02-23

    Mainstays Three-Wick Candles Recalled for Fire and Laceration Hazards

    Star Soap Star Candle Prayer Candle recalled about 1.2 million Mainstays Three-Wick Candles because the wicks can burn too close to the glass container, causing it to break and posing fire and laceration hazards. Consumers should stop using the candles immediately and request a refund.

    Product
    Mainstays Three-Wick Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23134·2023-02-23

    Lancaster Table & Seating High Chairs Recalled for Fall Hazard

    Clark Associates is recalling Lancaster Table & Seating brand high chairs that can break during use, posing a fall hazard to children. Three reports of high chairs breaking have been received, though no injuries have been reported.

    Product
    Lancaster Table & Seating brand High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23728·2023-02-23

    Polaris Timbersled Snow Bike Conversion Kits Recalled for Crash Hazard

    Polaris is recalling about 780 Timbersled snow bike conversion kits because a QuickDrive fastener can loosen during operation, causing brake failure and crash risk. No crashes or injuries have been reported.

    Product
    Polaris Timbersled Snow Bike Conversion Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23131·2023-02-23

    SCARPA F1 Ski Boots Recalled for Fall Hazard

    SCARPA North America is recalling about 770 F1 LT and F1 GT ski boots manufactured in 2022. Screws attaching the ski/walk mechanism can loosen or fall out, causing the mechanism to malfunction and posing a fall hazard.

    Product
    F1 LT and F1 GT Ski Boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23729·2023-02-23

    Harbor Freight Replacement Lower Blade Guards for 12-Inch Miter Saws

    Harbor Freight Tools is recalling replacement lower blade guards for 12-inch Chicago Electric Miter Saws because they do not sufficiently cover the saw blade and can break during use, posing an injury hazard.

    Product
    Replacement lower blade guards for 12-inch Chicago Electric Miter Saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V110000·2023-02-22

    2023 Lucid Air propulsion system electrical switches may fail unexpectedly

    Lucid is recalling certain 2022-2023 Air vehicles because electrically activated contactor switches in the propulsion system may unexpectedly open, cutting power to the electric motors and increasing the risk of a crash.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0321-2023·2023-02-22

    FDA Recalls TPN Nutrition Bags Due to Sterility Assurance Failure

    Sentara Infusion Services recalls 24 bags of TPN (Total Parenteral Nutrition) distributed nationwide due to lack of sterility assurance. The recall affects prescription intravenous nutrition products.

    Product
    TPN (a) 95GM/AA, 385/DEX, 50GM/LIP 1800ML, (b)TPN AA:100GM DEX:250GM LIP:50GM 2400ML, (c) TPN: AA 80GM ; DEX 320GM ; LIP 50GM IN 2300 ml, Rx only, use with Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0304-2023·2023-02-22

    Methadone Syringes Recalled for Lack of Sterility Assurance

    Sentara Infusion Services is recalling methadone syringes due to lack of sterility assurance. The affected product was dispensed to patients nationwide.

    Product
    METHADONE (a) 2.5MG IN 5ML NS SYRINGE, (b) 4MG IN 5ML NS SYRINGE, pain, Rx Only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1136-2023·2023-02-22

    Siemens Biograph Vision PET Scanner Gantry Locking Mechanism Recall

    Siemens recalls Biograph Vision PET scanners worldwide for a potential defect in the gantry locking mechanism that secures the equipment during scanning and service.

    Product
    SIEMENS Biograph Vision: a) 450, b) 600, c) 600 Edge
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0306-2023·2023-02-22

    Metronidazole injectable antibiotic recalled due to sterility concerns

    Sentara Infusion Services is recalling 30 bags of Metronidazole 500mg injectable antibiotic distributed nationwide due to lack of sterility assurance. Patients using the product should contact their healthcare provider.

    Product
    METRONIDAZOLE 500MG 100ML, antibiotic, Rx Only, use with a home pump or no pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0298-2023·2023-02-22

    INTRALIPID 18GM Parenteral Nutrition Recalled for Lack of Sterility Assurance

    Sentara Infusion Services is recalling 7 bags of INTRALIPID 18GM, a parenteral nutrition solution, due to lack of sterility assurance. The product was dispensed to patients nationwide.

    Product
    INTRALIPID 18GM, TPN, Rx Only, use with a Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0275-2023·2023-02-22

    Ampicillin IV Infusion Bags Recalled for Lack of Sterility Assurance

    Sentara Home Infusion Pharmacy Services is recalling 14 bags of Ampicillin 8GM in NS 400ML due to lack of sterility assurance. The affected batches were distributed nationwide to patients.

    Product
    AMPICILLIN 8GM IN NS 400ML, antibiotic, used with Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0309-2023·2023-02-22

    Mycamine 100mg Intravenous Preparation Recalled for Sterility Assurance Deficiency

    Sentara Infusion Services recalled Mycamine 100mg intravenous solution nationwide due to lack of sterility assurance. Patients should contact their healthcare provider.

    Product
    MYCAMINE 100MG IN NS 100ML, antifungal, Rx Only, use with a homepump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1126-2023·2023-02-22

    Surgical Instrument Trays Recalled for Compromised Outer Bag Sterility

    Medline Industries recalls CENTURION MEDICAL PRODUCTS IR INSTRUMENT TRAYS due to a perforated outer bag that fails to maintain sterility. While the inner contents remain sterile, the compromised outer bag could contaminate instruments during surgical procedures.

    Product
    Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS IR INSTRUMENT TRAY, Reorder Number SUT10675
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1118-2023·2023-02-22

    Surgical Convenience Kits Recalled Due to Compromised Sterility of External Wrapping

    Medline Industries is recalling 630 surgical convenience kits because the perforated bag design fails to maintain sterility of the outer wrapping, though internal contents remain sterile.

    Product
    Surgical convenience kits labeled as: a) MEDLINE GENERAL UTILITY, Reorder Number DYNDA2524 b) CENTURION MEDICAL PRODUCTS DIALYSIS ON/OFF BUNDLE, Reorder Number DT22705A c) CENTURION MEDICAL PRODUCTS ULTRASOUND PIV BUNDLE, Reorder Number IV8635D d) CENTURION MEDICAL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1119-2023·2023-02-22

    Surgical kits recalled due to compromised sterile wrapping

    Medline Industries is recalling multiple CENTURION MEDICAL PRODUCTS surgical kits because perforated packaging compromises the sterile barrier. Only contents inside the kit wrapping maintain sterility.

    Product
    Surgical convenience kits labeled as: a) CENTURION MEDICAL PRODUCTS CHEST TUBE INSERTION TRAY, Reorder Number CVI2105; b) CENTURION MEDICAL PRODUCTS VASECTOMY KIT, Reorder Number MNS11975; c) CENTURION MEDICAL PRODUCTS LACERATION TRAY, Reorder Number SUT11670; d)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0267-2023·2023-02-22

    Injectable Vitamin B Vials Recalled for Particulate Matter Contamination

    McGuff Compounding Pharmacy recalls 255 vials of thiamine and riboflavin injection nationwide due to foreign substances found in some vials.

    Product
    Thiamine Hydrochloride 3000 mg/30 mL (100mg/mL), Riboflavin 30 mg/30 mL (1mg/mL) Injection, FOR INTRAMUSCULAR OR SLOW INTRAVENOUS USE, 30 mL Sterile Multiple Use Vial, Rx Only, Compounded for a licensed professional or patient use by: McGuff Compounding Pharmacy Services, Inc…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0297-2023·2023-02-22

    Antibiotic Injectable Recalled for Lack of Sterility Assurance

    Sentara Infusion Services is recalling an antibiotic injectable medication due to lack of sterility assurance. Seven bags were dispensed to patients nationwide with a Beyond Use Date of December 2022.

    Product
    IMIPENEM/CILASTATIN 2000MG IN NS 400ML, antibiotic, Rx Only, use with a Curlin Pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320, NDC# 63323-0322-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0273-2023·2023-02-22

    Amikacin Injectable Antibiotic Lacks Sterility Assurance, Nationwide Recall

    Sentara Infusion Services is recalling 7 bags of Amikacin 450MG injectable antibiotic due to lack of sterility assurance. The product was dispensed nationwide to patients receiving IV infusions.

    Product
    Amikacin 450MG IN NS 45ML, Antibiotic, used in a HOMEPUMP, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300 Chesapeake, VA 23320,
    Category
    Drug
    Distribution
    Distributed nationwide