The Recall Desk

State

US Virgin Islands product recalls

73,718 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.

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30276–30300 of 73896

  • HighNHTSA·20E004000·2020-02-06

    Freedman Seat Belt Retractor Recall for Improper Occupant Securing

    Freedman Seating Company is recalling certain seat assemblies because the seat belt retractor block out zone may not be set correctly, potentially failing to secure occupants.

    Product
    SEAT BELTS:FRONT:RETRACTOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20070·2020-02-06

    DR Walk-Behind Leaf Blowers Recalled for Projectile Hazard

    Country Home Products is recalling specific DR walk-behind leaf blowers because internal blades can break off and discharge, posing a projectile hazard.

    Product
    Leaf blowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20071·2020-02-06

    Infantino Recalls Infant Carriers Due to Buckle Breakage and Fall Hazard

    Infantino is recalling about 14,000 infant carriers because the buckles can break, posing a fall hazard. No injuries have been reported.

    Product
    Go Forward 4-in-1 Evolved Ergonomic, Flip Front2back and Up Close Newborn infant carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0864-2020·2020-02-05

    Radiometer AQURE basic system software recall for patient data mix-up risk

    Radiometer Medical ApS is recalling AQURE basic system software versions 2.3.5 and below due to a potential patient data mix-up risk when connected to third-party devices.

    Product
    AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use: The AQURE system is intended to let you manage analytical devices and operator profiles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0563-2020·2020-02-05

    Whole Foods Recalls Dark Chocolate Peppermint Sandwiches for Undeclared Milk

    Whole Foods Market is recalling 365 Everyday Value Dark Chocolate Peppermint Sandwich Cremes because they may contain undeclared milk.

    Product
    365 Everyday Value Dark Chocolate Peppermint Sandwich Cremes Net Wt 7.75 oz (220g) UPC 9948247605 Paper carton boxes sold individually
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0822-2020·2020-02-05

    Walgreens Acne Cleansing Bar Recalled for Metal Contaminant

    Shandex Personal Care Manufacturing Inc. is recalling Walgreens Acne Cleansing Bar due to the presence of a visible metal contaminant.

    Product
    Walgreens Acne Cleansing Bar, Benzoyl Peroxide 10%, NET WT 4 oz (113 g), 1 bar per carton, Distributed By: Walgreen Co., 200 Wilmot Road, Deerfield, IL 60015, NDC: 0363-0137-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0564-2020·2020-02-05

    Whole Foods Recalls Dark Chocolate Caramel Sea Salt Sandwich Cremes

    Whole Foods Market is recalling 365 Everyday Value Dark Chocolate Caramel Sea Salt Sandwich Cremes due to potential undeclared milk and coconut.

    Product
    365 Everyday Value Dark Chocolate Caramel Sea Salt Sandwich Cremes Net Wt 7.75 oz (220g) UPC 9948247606 Paper carton boxes sold individually
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0905-2020·2020-02-05

    Haemonetics Recalls Cell Saver Bowl Sets Due to Leak Risk

    Haemonetics is recalling specific Cell Saver bowl sets because they may leak, potentially trapping fluid and causing incomplete washing.

    Product
    Japan DISP SET, 263J, 205J, 208 - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0898-2020·2020-02-05

    Haemonetics Recalls Cell Saver Bowl Sets Due to Leak Risk

    Haemonetics is recalling Cell Saver bowl sets because cracks in the inner core may cause leaks and incomplete blood washing.

    Product
    JAPAN BASIC HI SPEED CS5 SET,LN 263J - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma. The recovered blood is processed by a centrifugation and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0868-2020·2020-02-05

    LivaNova Recalls Cyberonics VNS Therapy AspireHC Model 105 Generators

    LivaNova USA Inc is recalling 106 Cyberonics VNS Therapy AspireHC Model 105 generators due to electrical leakage causing premature battery depletion.

    Product
    Cyberonics VNS Therapy AspireHC Model 105 Generator, 26-0007-4000/3. The firm name on the label is CYBERONICS, INC., Houston, TX. Vagus nerve stimulator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0900-2020·2020-02-05

    Haemonetics Recalls Cell Saver Bowl Sets Due to Leak Risk

    Haemonetics is recalling 739 Cell Saver bowl sets because cracks in the inner core can cause leaks and incomplete blood washing.

    Product
    JAPAN DISP SET, 261J, 205J, HAR - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma. The recovered blood is processed by a centrifugation and washing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0892-2020·2020-02-05

    Haemonetics Recalls CS Elite Processing Sets Due to Potential Bowl Cracks

    Haemonetics is recalling CS Elite Processing Sets because cracks in the bowl core may cause fluid trapping and incomplete washing.

    Product
    CS Elite Processing Set (225 ml) Autotransfusion Device - Product Usage:its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0855-2020·2020-02-05

    Vitreq Recalls VitreQ 23G Silicone Tipped Cannula Due to Sterility Concerns

    Vitreq Bv is recalling VitreQ 23G Silicone Tipped Cannulas because microscopic tears in the sterile pouch may compromise sterility.

    Product
    VitreQ 23G Silicone Tipped Cannula-CN23.D01 GTIN: 8719214221508
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0848-2020·2020-02-05

    Vitreq 20G Needles Recalled for Potential Sterility Compromise

    Vitreq Bv is recalling VitreQ 20G Blunt and Brush Needles because microscopic tears in the sterile pouch may compromise sterility.

    Product
    (1) VitreQ 20G BF Blunt Needles-Ref: BF20.D51 GTIN: 8719214221089 (2) VitreQ 20G BF Brush Needles-REF: BF20.D52 GTIN: 8719214221102
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0852-2020·2020-02-05

    Vitreq Recalls VitreQ 25G VFI Cannulas Due to Sterility Concerns

    Vitreq Bv is recalling VitreQ 25G VFI Cannulas because microscopic tears in the sterile pouch may compromise sterility.

    Product
    VitreQ 25G VFI Cannula-REF: CN25.D03 GTIN: 8719214221447
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0890-2020·2020-02-05

    Haemonetics Recalls Cell Saver Fastpacks Due to Potential Bowl Cracks

    Haemonetics is recalling 8,641 Cell Saver 5/5+ Fastpacks because cracks in the bowl core can trap fluid, causing incomplete washing and device errors.

    Product
    CS5/5+ Fastpacks, 225 mL, 20¿ Res Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0894-2020·2020-02-05

    Haemonetics Recalls CS Elite Fastpack Autotransfusion Devices Due to Leak Risk

    Haemonetics is recalling CS Elite Fastpack autotransfusion devices because cracks in the bowl core may cause leaks and incomplete blood washing.

    Product
    CS Elite Fastpack, 225 mL, 20¿ Res Autotransfusion Device - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0886-2020·2020-02-05

    Haemonetics Recalls CS5/5+ Bowl Kits Due to Potential Leaks

    Haemonetics is recalling CS5/5+ Bowl Kits because potential leaks may trap fluid, causing device errors and incomplete washing.

    Product
    CS5/5+ Bowl Kit-125 mL Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0903-2020·2020-02-05

    Haemonetics Recalls Cell Saver Elite Sets Due to Potential Bowl Leaks

    Haemonetics is recalling Cell Saver Elite sets because potential leaks in the bowl core may cause fluid trapping and incomplete washing.

    Product
    JAPAN CELL SAVER ELITE SET - 125ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and pumping this…
    Category
    Medical Device
    Distribution
    Distributed nationwide