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.

54901–54925 of 74002

  • ModerateFDA (Food)·F-1718-2015·2015-04-08

    Health One Pharmaceuticals Recalls Fish Oil 200 for cGMP Violations

    Health One Pharmaceuticals is recalling Fish Oil 200 dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Fish Oil 200
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1744-2015·2015-04-08

    Health One Pharmaceuticals Recalls Passion Secret Dietary Supplements

    Health One Pharmaceuticals is recalling Passion Secret dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Passion Secret
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1671-2015·2015-04-08

    Health One Pharmaceuticals Recalls Four Things Combination Dietary Supplement

    Health One Pharmaceuticals is recalling Four things Combination dietary supplements due to significant violations of current good manufacturing practices (cGMP) regulations.

    Product
    Four things Combination, 100 Vegetarian Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1366-2015·2015-04-08

    Owen Mumford Autoject E1 Fixed Needle Device Recalled for Missing Components

    Owen Mumford USA, Inc. is recalling 3,100 Autoject E1 Fixed needle devices because the syringe carrier is missing a damper and spring.

    Product
    Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by patients to inject drugs as prescribed by their doctor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1658-2015·2015-04-08

    Health One Pharmaceuticals Recalls Protein Mix for cGMP Violations

    Health One Pharmaceuticals is recalling Protein Mix dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Protein Mix
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1353-2015·2015-04-08

    Stryker Recalls Vitagel Surgical Hemostat Due to Cold Chain Violations

    Stryker Orthobiologics is recalling Vitagel surgical hemostat shipments that were not delivered within validated timeframes, potentially compromising the product's required cold storage.

    Product
    Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1660-2015·2015-04-08

    Health One Pharmaceuticals Recalls Herbal Health Dietary Supplements

    Health One Pharmaceuticals is recalling Herbal Health dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Herbal Health
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1358-2015·2015-04-08

    Bard Urinary Drainage Bags Recalled for Potential Sterile Barrier Breach

    C.R. Bard is recalling specific lots of urinary drainage bags due to a potential breach of the sterile barrier packaging.

    Product
    Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot # NGYJ0603 and NGYJ1671
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1349-2015·2015-04-08

    Microtek Medical recalls sterile smoke evacuator wands due to latex packaging

    Microtek Medical is recalling sterile smoke evacuator wands because the packaging contains latex but lacks the required warning label.

    Product
    INTEGRAL WAND W/TUBING, STERILE, REF 24185, QTY 24/CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms, Trauma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1352-2015·2015-04-08

    Synthes Aiming Arms Recalled Due to Potential Jamming of Guide Sleeve

    Synthes, Inc. is recalling 131 Aiming Arms from the TFN-ADVANCED system because the guide sleeve may jam, potentially delaying instrument removal.

    Product
    Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm; The 130 Degree Aiming Arm and 125 Degree Aiming Arm are a part of the TFN-ADVANCED (TFNA) System. The TFN-ADVANCED Proximal Femoral Nailing System is intended for treatment of fractures in adults and adolescents (12-21)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1676-2015·2015-04-08

    Health One Pharmaceuticals Recalls Reishi Spore Gen Dietary Supplements

    Health One Pharmaceuticals is recalling Reishi Spore Gen dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Reishi Spore Gen, 90 Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1340-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmets Due to Latex Packaging

    Microtek Medical Inc is recalling 11 units of Freedomaire Surgical Helmet Systems because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET SYSTEM WITH BELT, REF 11114STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical personnel in order to protect against…
    Category
    Medical Device
    Distribution
    Distributed nationwide