The Recall Desk

State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55751–55775 of 74005

  • ModerateFDA (Devices)·Z-0852-2015·2014-12-31

    Getinge 46-Series Medical Washer-Disinfector Recalled for Sediment Residuals

    Getinge Disinfection AB is recalling 46-Series Medical Washer-Disinfector models 46-4 and 46-5 due to sediment residuals in the manifold caused by air pockets.

    Product
    GETINGE 46-SERIES Medical Washer-Disinfector, Models 46-4 and 46-5, with PACS 300/350 Control Series with dryer --- Class II, exempt from 510(k) requirements. For use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0834-2015·2014-12-31

    Intuitive Surgical Recalls Fluorescence Imaging Procedure Kits for Missing Storage Info

    Intuitive Surgical is recalling Fluorescence Imaging Procedure Kits because storage conditions for indocyanine green are missing from the packaging.

    Product
    Fluorescence Imaging Procedure Kit, designed for use with Firefly Fluorescence Imaging for the da Vinci Si 3000 Surgical Systems. The Intuitive Surgical Endoscopic Instrument Control System (Intuitive Surgical da Vinci Surgical System Model IS3000) is intended to assist in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0835-2015·2014-12-31

    Intuitive Surgical Recalls Fluorescence Imaging Procedure Kits for Missing Storage Info

    Intuitive Surgical is recalling Fluorescence Imaging Procedure Kits because storage conditions for indocyanine green are missing from the packaging.

    Product
    Fluorescence Imaging Procedure Kit, designed for use with Firefly Fluorescence Imaging for the da Vinci Xi 4000 Surgical Systems. The Intuitive Surgical Endoscopic Instrument Control System (Intuitive Surgical da Vinci Surgical System Model IS3000) is intended to assist in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0833-2015·2014-12-31

    GE Healthcare Recalls Centricity Enterprise Archive Software Due to Data Loss Risk

    GE Healthcare is recalling Centricity Enterprise Archive software versions 4.0.x due to a potential data loss issue associated with HL-7 updates.

    Product
    Centricity Enterprise Archive is a software product for receiving, archiving and sending of medical data. DICOM devices (e..g. modalities, workstations) Communicate with the archive using the DICOM protocol (published by ACR-NEMA). The clinical use is limited to the interaction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0860-2015·2014-12-31

    Siemens ADVIA Centaur XP Immunoassay System Recalled for Tubing Crack Risk

    Siemens Healthcare Diagnostics is recalling 10,515 ADVIA Centaur XP Immunoassay Systems because a slight crack may occur in the tubing at the reservoir connector assembly due to mechanical stress.

    Product
    ADVIA Centaur XP Immunoassay System (including refurbished) Professional use in a laboratory for in vitro diagnostic tests.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0321-2015·2014-12-31

    KC Pharmaceuticals Recalls Eye Drops Due to Non-GMP API Storage

    KC Pharmaceuticals is recalling 302,976 bottles of Eye Drops A.C. because the active ingredient was stored in a non-GMP compliant warehouse in Italy.

    Product
    Eye Drops A.C. (Tetrahydrozoline HCl 0.05%, Zinc sulfate 0.25%), 0.5 FL OZ (15 mL) Bottles, Over the Counter. Labeled: a) Astringent Redness Reliever, Distributed by Safeway Inc., P.O. Box 99, Pleasanton, CA 94566-0009, UPC: 3 21130 70067 8; b) Best Choice, Distributed By: Valu…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0322-2015·2014-12-31

    K C Pharmaceuticals Recalls Eye Drops Due to Warehouse Storage Issues

    K C Pharmaceuticals is recalling specific lots of Eye Drops Industrial Strength because the active ingredient was stored in a non-GMP compliant warehouse in Italy.

    Product
    Eye Drops Industrial Strength (Polyethylene glycol 400 1%, Tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15 mL) Bottles, Over the Counter. Labeled: a) Manufactured for: Petragon, Inc., Edwardsville, KS 66111; b) SWIFT, Distributed by Swift First Aid, Inc., Valencia, Calif. 91355…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0323-2015·2014-12-31

    KC Pharmaceuticals Recalls Sunmark Eye Drops for CGMP Deviations

    KC Pharmaceuticals is recalling Sunmark Eye Drops Advanced Moisturizer/Lubricant because the active ingredient was stored in a non-GMP compliant warehouse in Italy.

    Product
    SUNMARK EYE DROPS ADVANCED MOISTURIZER/LUBRICANT — SUNMARK EYE DROPS ADVANCED MOISTURIZER/LUBRICANT (DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0318-2015·2014-12-31

    Sulfur8 Medicated Anti-Dandruff Conditioner Recalled for pH Specification Failure

    J. Strickland and Co is recalling Sulfur8 Medicated Anti-Dandruff Conditioner because the product pH failed to meet specifications.

    Product
    sulfur8(R) medicated anti-dandruff conditioner, dandruff treatment for Braids, spray, Active Ingredient: Salicylic Acid, 2%, 12 FL OZ (356ml) spray bottle, OTC, Made in the U.S.A. J. Strickland & Co., OLIVE BRANCH, MS 38654 UPC: 0 7561044510 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0313-2015·2014-12-31

    Hospira Recalls Dacarbazine Injection Vials Due to Discoloration

    Hospira Inc. is recalling 3,306 vials of Dacarbazine Injection, USP, 200mg, because the reconstituted solution may appear pink instead of the expected colorless to pale yellow.

    Product
    Dacarbazine, Injection, USP, 200mg, vials packaged in individual cartons, Rx only, Manufactured by Hospira Australia 1 Lexia Place, Mulgrave, Victoria Australia 3170. NDC 61703-327-22.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V827000·2014-12-30

    GM Recalls 2011-2012 Trucks and SUVs for Ignition Lock Defect

    General Motors is recalling 84,192 vehicles because the ignition lock may bind or stick, potentially causing loss of steering and braking power.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SUBURBAN, AVALANCHE, SILVERADO, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V826000·2014-12-30

    Dodgen Recalls 2014-2015 RVs for Suspension Tank Bracket Failure Risk

    Dodgen is recalling 2014-2015 Born Free RVs equipped with Liquid Spring suspension kits because a mounting bracket may fail, causing the fluid tank to separate and create a road hazard.

    Product
    DODGEN — DODGEN BORN FREE, BORN FREE MOBILITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V829000·2014-12-30

    Spartan Recalls 2015 K3 Chassis Due to Steering Slip Shaft Wear

    Spartan Motors is recalling 32 model year 2015 K3 Chassis vehicles because the steering slip shaft may prematurely wear, increasing the risk of a vehicle crash.

    Product
    SPARTAN — SPARTAN K3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V828000·2014-12-30

    Toyota and Scion Recall for Improperly Installed Accessories

    Southeast Toyota Distributors is recalling 2014-2015 Toyota and Scion vehicles because accessories like running boards may have been installed with improperly tightened fasteners.

    Product
    SCION — SCION, TOYOTA XB, RAV4, LAND CRUISER, FJ CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V810000·2014-12-29

    PACCAR Recalls 2015 Kenworth and Peterbilt Trucks for Brake Drag Risk

    PACCAR is recalling 1,623 model year 2015 Kenworth and Peterbilt trucks because an improperly seated diaphragm in the air brake actuators may cause brake drag and wheel end fires.

    Product
    KENWORTH — KENWORTH, PETERBILT T270, T470, 567, 587
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V824000·2014-12-29

    Porsche Recalls 2015 Cayenne Vehicles for Suspension Alignment Defect

    Porsche is recalling specific 2015 Cayenne Diesel and Cayenne S vehicles because incorrect suspension alignment may reduce vehicle handling and increase crash risk.

    Product
    PORSCHE — PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V825000·2014-12-29

    Dodgen Recalls Mobility RVs Due to Wheelchair Lift Platform Cracking Risk

    Dodgen is recalling 2006-2014 Mobile Tech. Mobility RVs equipped with specific Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.

    Product
    DODGEN — DODGEN MOBILE TECH. MOBILITY RV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0735-2015·2014-12-24

    B&G Foods Recalls Ortega Taco Seasoning for Peanut and Almond Allergens

    B&G Foods is recalling Ortega and Las Palmas taco seasoning and kits because spice ingredients may contain peanuts and almonds.

    Product
    Taco Seasoning Packets sold under the following brands, container size, and or as part of a dinner Kit: 1. Ortega 1.25 oz, UPC 39000-00820; 2. Ortega 3-pack, 3.75 oz. UPC 39000-00821; 3. Ortega Foodservice 5 lb. UPC 39000-00860 and 9 oz. 39000-00861; 4. Las…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0740-2015·2014-12-24

    Ortega Taco Sauce Recalled for Potential Peanut and Almond Contamination

    B&G Foods is recalling Ortega Taco Sauce and other products because spice ingredients may contain undeclared peanuts and almonds.

    Product
    Ortega Taco Sauce - Hot 8 oz, UPC 39000-00891, 16 oz. UPC 41501-01895.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0739-2015·2014-12-24

    Ortega Taco Sauce Recalled for Potential Peanut and Almond Contamination

    B&G Foods is recalling Ortega Taco Sauce and other products because spice ingredients may contain undeclared peanuts and almonds.

    Product
    Ortega Taco Sauce - Medium 8 oz, UPC 39000-01892, 16 oz. UPC 39000-01894.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V819000·2014-12-24

    GM Recalls 2015 Silverado and Sierra Trucks for Rear Axle Fracture Risk

    General Motors is recalling specific 2015 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because the rear axle shaft may fracture, potentially causing the rear wheel to separate.

    Product
    GMC — GMC, CHEVROLET SIERRA, SILVERADO
    Category
    Vehicle
    Distribution
    Distributed nationwide