The Recall Desk

State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

60126–60150 of 74011

  • ModerateFDA (Devices)·Z-0504-2014·2013-12-25

    Stryker Neurovascular Medical Devices Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates exceeding available shelf-life data.

    Product
    Stryker brand GDC VORTX 2MM X 3MM, Catalog Number: M00335302340; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0789-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive Supplement Due to Chloramphenicol

    National Enzyme Co is recalling bulk B807 True Botanica Digestive dietary supplements because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk B807 True Botanica Digestive, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83377);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-351-2014·2013-12-25

    Tween Brands Recalls Hand Sanitizer with Incorrect Alcohol Labeling

    Tween Brands is recalling 42,570 units of Green Apple hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.

    Product
    Girls can change the World, Green Apple Anti bac Justice, Ethyl Alcohol, Net Wt 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5 Made in China
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0512-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates that exceed available shelf-life data.

    Product
    Stryker brand SUPER COMPLIANT 7MM X 15MM, Catalog Number: M003SSC07150; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0535-2014·2013-12-25

    3M ESPE Imprint II and Paradigm Impression Materials Recalled for Quality Issues

    3M is recalling specific lots of Imprint II and Paradigm dental impression materials because a defect reduces moisture displacement, potentially affecting impression quality.

    Product
    3M ESPE Imprint II Regular Body , Catalog Number 9379, and Paradigm Regular Body VPS, Catalog Number 5315, Impression Material that are intended to reproduce the structure of a patients teeth. Impression Materials are composed of hydrophilic vinyl polysiloxane impression…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0527-2014·2013-12-25

    Karl Storz Recalls Flexible Broncho Fiberscopes Due to Material Issue

    Karl Storz Endoscopy America is recalling 141 flexible broncho fiberscopes because the suction channel material is not listed for STERRAD sterilization systems.

    Product
    Broncho Flexible Fiberscope, models: 11001BN1, 11002BD1, 11004BC1, and 11009BC1. " Examination and treatment of the tracheobronchial tree Contraindications for Bronchoscopy " Uncontrolled angina, uncontrolled heart failure, or serious uncontrolled ventricular arrhythmias "…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0756-2014·2013-12-25

    National Enzyme Recalls GreenPlanet Enzymeblend Powder Due to Chloramphenicol

    National Enzyme Co is recalling GreenPlanet Enzymeblend Powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk 7775 GreenPlanet Enzymeblend Powder packaged in poly bags within fiber drums (SKU 82566)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0500-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling specific microcatheter and coil products because they were shipped with use-by dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED 90 150CM, Catalog Number: M0031681910; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0801-2014·2013-12-25

    National Enzyme Recalls Travnie Extra Due to Potential Chloramphenicol Contamination

    National Enzyme Co is recalling Travnie Extra dietary supplements because they may contain chloramphenicol above 0.3 ppb.

    Product
    Enzyme - Travnie Extra, Formula C500, packaged in 30-capsule bottles (SKU 54513). Firm name on the label is National Enzyme Company;
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0515-2014·2013-12-25

    Instrumentation Laboratory Recalls HemosIL Low Abnormal Control 2 Kits

    Instrumentation Laboratory is recalling 6,504 kits of HemosIL Low Abnormal Control 2 UNASSAYED because the product lacks FDA 510(k) approval.

    Product
    HemosIL Low Abnormal Control 2 UNASSAYED Part Number: 0020003220
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-349-2014·2013-12-25

    Tween Brands Recalls Share a Smile Hand Sanitizer Due to Label Error

    Tween Brands Inc is recalling Share a Smile Mixed Berry hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.

    Product
    Share a Smile Mixed berry Anti bac Justice, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0497-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling Excelsior SL-10 microcatheters because they were shipped with use-by dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED S 15OCM; Catalog Number: M0031441920; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0783-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive Blend Powder Due to Chloramphenicol

    National Enzyme Co is recalling bulk A977 Wedar Digestive Blend 2 powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk A977 Wedar Digestive Blend 2 powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83314);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0802-2014·2013-12-25

    National Enzyme Recalls Bulk Vitakost Low Carb Diet Due to Chloramphenicol

    National Enzyme Co is recalling Bulk C542 Vitakost Low Carb Diet because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk C542 Vitakost Low Carb Diet, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92544);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0543-2014·2013-12-25

    CooperVision Recalls ClearSight Toric Contact Lenses for Incorrect Expiration Dates

    CooperVision is recalling specific lots of ClearSight Toric 1 day contact lenses because the outer cartons display incorrect expiration dates, though the inner blisters are correct.

    Product
    ClearSight(TM) Toric 1 day (ocufilcon D), 30 daily disposable contact lenses for astigmatism, STERILE, Rx only --- CooperVision Hamble, SO31 4RF, UK - Scottsville, NY 14546 USA - Juana Diaz, PR 00795 USA daily use disposable contact lenses for astigmatism
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0796-2014·2013-12-25

    National Enzyme Recalls BioSan Enzyme Blend Capsules Due to Chloramphenicol

    National Enzyme Co is recalling BioSan Enzyme Blend 3 O capsules because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk C012 BioSan Enzyme Blend 3 O capsules,packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92438);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0499-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Shelf-Life Labeling Errors

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED 45 150CM, Catalog Number: M0031681900, Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0809-2014·2013-12-25

    National Enzyme Recalls ZoiVi Digestive Formula Powder Due to Chloramphenicol

    National Enzyme Co is recalling ZoiVi Digestive Formula powder because it may contain chloramphenicol above 0.3 ppb.

    Product
    Bulk C812 ZoiVi Digestive Formula powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83438)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0755-2014·2013-12-25

    National Enzyme Recalls Dietary Supplements Due to Potential Chloramphenicol Contamination

    National Enzyme Co is recalling specific dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configurations: (1) 7263 Kirk Enz-Comp-W-TG UNL, packaged in unlabeled, 90-capsule bottles (SKU 52939); (2) 7263 Kirk Enz-Comp-W-TG UNL2, packaged in unlabeled 180-capsule bottles (SKU 53852);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0805-2014·2013-12-25

    National Enzyme Recalls Colon Health Support Due to Chloramphenicol

    National Enzyme Co is recalling Healthy Reflections Colon Health Support supplements because a raw material may contain chloramphenicol above 0.3 ppb.

    Product
    Healthy Reflections, Colon Health Support, packaged 120-capsule bottles (SKU 54554). Firm name on the label is Healthy Reflections, Garfield, MN;
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0495-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Shelf-Life Labeling Errors

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates that exceed available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM; Catalog Number: M0031441930; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0779-2014·2013-12-25

    National Enzyme Recalls Bulk Enzyme Powder for Potential Chloramphenicol

    National Enzyme Co is recalling bulk enzyme powder that may contain chloramphenicol above 0.3 ppb.

    Product
    Bulk A322 Houston Chewable Enzyme powder (SKU 83226), packaged in varying quantities within poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0741-2014·2013-12-25

    National Enzyme Co Recalls Wellzymes Digestive Health Enzyme Supplement

    National Enzyme Co is recalling Wellzymes Digestive Health Enzyme Supplement bottles because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    WELLZYMES, Digestive Health, Enzyme Supplement packaged in 60-(SKU 52235) capsule bottles. Manufactured exclusively for enzymes, inc. Kansas City, MO
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0501-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling certain microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM, Catalog Number: M0031681920; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide