The Recall Desk

State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53051–53075 of 74002

  • HighFDA (Food)·F-2423-2015·2015-07-15

    New Punjab Kaju Roll Recalled for Undeclared Cashews and Colors

    New Punjab Sweets Inc. is voluntarily recalling Kaju Roll snacks because they may contain undeclared cashews and artificial colors Yellow 5 and 6.

    Product
    New Punjab Kaju Roll is an Indian snack cut into squares. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2041-2015·2015-07-15

    Stradis Arthroscopy Packs Recalled Due to Component Recall

    Stradis Healthcare is recalling Arthroscopy Packs because they contain Devon Light Gloves, which are being recalled by the manufacturer Medtronic.

    Product
    Arthroscopy Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2422-2015·2015-07-15

    New Punjab Kaju Katri Recalled for Undeclared Cashews and Colors

    New Punjab Sweets Inc. is voluntarily recalling Kaju Katri Indian snacks because they may contain undeclared cashews and artificial colors Yellow 5 and 6.

    Product
    New Punjab Kaju Katri is an Indian snack cut into squares. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V448000·2015-07-15

    Spartan Emergency Response Vehicles Recalled for Valve Stem Wear

    Spartan is recalling 2007-2015 emergency response vehicles because front wheel valve stems may rub against brake calipers, causing sudden tire deflation.

    Product
    SPARTAN — SPARTAN GLADIATOR, METROSTAR, ADVANTAGE, DIAMOND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2045-2015·2015-07-15

    Volcano ComboMap Intravascular System Recalled for Interoperability Limitation

    Volcano Corp is recalling 227 ComboMap Intravascular Flow and Pressure Systems due to a limitation in interoperability with the Philips Xper Flex Cardia Physiomonitoring System.

    Product
    ComboMap Intravascular Flow and Pressure System; Product/Part number: Combo Map - 802745-001. Intravascular Imaging and Pressure System for evaluation of blood flow, perfusion and vascular structures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2023-2015·2015-07-15

    Stradis Healthcare Recalls Eye Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling Eye Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.

    Product
    Eye Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2021-2015·2015-07-15

    Stradis Gyn Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Gyn Packs containing Devon Light Gloves because the manufacturer, Medtronic, recalled the glove component.

    Product
    Gyn Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2019-2015·2015-07-15

    Stradis Healthcare Recalls Abdominal Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling Abdominal Packs and Abdom Packs because they contain Devon Light Gloves, a component recalled by Medtronic.

    Product
    Abdominal Pack and Abdom Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2012-2015·2015-07-15

    Stradis ACL Pack Recalled Due to Component Glove Recall

    Stradis Healthcare is recalling ACL Packs containing Devon Light Gloves because the manufacturer, Medtronic, is recalling the glove component.

    Product
    ACL Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2017-2015·2015-07-15

    Stradis Healthcare Recalls Bariatric Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling Bariatric Packs because they contain Devon Light Gloves that are subject to a separate manufacturer recall by Medtronic.

    Product
    Bariatric Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1995-2015·2015-07-15

    Stradis Vein Surgery Packs Recalled Due to Component Issue

    Stradis Healthcare is recalling 55 vein surgery packs because they contain a Devon Light Glove component subject to a separate recall by Medtronic.

    Product
    Vein Pack, Vein Treatment II Pack, Vein Brunswick Pack, Vein No Lidocaine Pack, Vein Ablation Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1230-2015·2015-07-15

    Zonisamide capsules recalled for inadequate complaint investigation

    American Health Packaging is recalling Zonisamide capsules due to current good manufacturing practice deviations involving inadequate investigation of customer complaints.

    Product
    Zonisamide capsules, USP 100mg packaged in 10-count blisters (NDC 68084-008-11); 5 blister packs per carton (NDC 68084-008-65); Rx only, Manufactured by: Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt, USA, LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA for…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2008-2015·2015-07-15

    Stradis Mississippi Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Mississippi Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.

    Product
    Mississippi Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2015-2015·2015-07-15

    Stradis Healthcare Recalls Skin and Vein Packs Containing Recalled Gloves

    Stradis Healthcare is recalling Skin and Vein Packs because they contain Devon Light Gloves that Medtronic is recalling.

    Product
    Skin and Vein Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2044-2015·2015-07-15

    Volcano Intravascular Ultrasound System Recalled for Interoperability Limitation

    Volcano Corp is recalling 227 Intravascular Ultrasound Imaging and Pressure Systems due to a limitation in interoperability with the Philips Xper Flex Cardia system that may impact Fraction Flow Reserve calculations.

    Product
    Volcano s5i/s5ix/s5iz/CORE Intravascular Ultrasound Imaging and Pressure System; Product/Part numbers: s5i -806300-020 ; s5ix/s5iz - 807400-001; CORE - 400-0 I 00.02. Intravascular Imaging and Pressure System for evaluation of blood flow, perfusion and vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1226-2015·2015-07-15

    American Health Packaging Recalls Lisinopril Tablets Due to CGMP Deviations

    American Health Packaging is recalling 4,718 cartons of Lisinopril 5mg tablets due to inadequate investigation of customer complaints.

    Product
    Lisinopril tablets, USP 5mg packaged in 10-count blisters (NDC 68084-060-11); 10 blister packs per carton (NDC 68084-060-01); Rx only, Manufactured by: Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt, USA, LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA for American…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2043-2015·2015-07-15

    Volcano Intravascular Ultrasound System Recalled for Interoperability Limitation

    Volcano Corp is recalling 227 intravascular ultrasound systems due to a limitation that may affect Fraction Flow Reserve calculations when connected to specific Philips monitors.

    Product
    Volcano s5/s5x/CORE Mobile Intravascular Ultrasound Imaging and Pressure System; Product/Part numbers: s5 - 804200-002 and 804200-014; s5x - 807300-001; CORE MOBILE - 400-0100.01. Intravascular Imaging and Pressure System for evaluation of blood flow, perfusion and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2025-2015·2015-07-15

    Stradis Healthcare Recalls Shoulder Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling surgical shoulder packs because they contain Devon Light Gloves that are subject to a separate manufacturer recall by Medtronic.

    Product
    Shoulder Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1225-2015·2015-07-15

    Famotidine tablets recalled for inadequate complaint investigation

    American Health Packaging is recalling 97,837 cartons of Famotidine tablets 20mg due to CGMP deviations involving inadequate investigation of customer complaints.

    Product
    Famotidine tablets, USP 20mg, packaged in 10-count blisters (NDC 68084-172-11); 10 blister packs per carton (NDC 68084-172-01); Rx only, Manufactured by: Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt, USA, LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA for…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2007-2015·2015-07-15

    Stradis Surgical Packs Recalled Due to Medtronic Glove Component Issue

    Stradis Healthcare is recalling surgical and general surgery packs because they contain Devon Light Gloves, a component being recalled by Medtronic.

    Product
    Surgical Pack and General Surgery Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide