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.

53676–53700 of 74002

  • HighFDA (Food)·F-2363-2015·2015-06-10

    Amy's Gluten Free Vegetable Lasagna Recalled for Listeria Risk

    Amy's Kitchen is recalling Gluten Free Vegetable Lasagna because supplier-confirmed Listeria monocytogenes was found in spinach used in the product.

    Product
    Amy's Gluten Free Vegetable Lasagna, 4.7 oz. 6 boxes per case. Amy Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2359-2015·2015-06-10

    Amy's Gluten Free Tofu Scramble Breakfast Wraps Recalled for Listeria

    Amy's Kitchen is recalling Gluten Free Tofu Scramble Breakfast Wraps because a spinach supplier notified them that the ingredient contained Listeria monocytogenes.

    Product
    Amy's Gluten Free Tofu Scramble Breakfast Wraps, 5.5 oz 156 g) 12 boxes per case. UPC: 0-42272-00807-0, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2361-2015·2015-06-10

    Amy's Brown Rice & Vegetables Bowl Recalled for Listeria Risk

    Amy's Kitchen is recalling Brown Rice & Vegetables Bowls because a supplier notified them that spinach used in manufacturing contained Listeria monocytogenes.

    Product
    Amy's Brown Rice & Vegetables Bowl, Light in Sodium, 9.5 oz (269 g) 12 boxes per case. UPC: 0-42272-00240-5, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1694-2015·2015-06-10

    Zimmer Recalls 4.5mm Cortical Screws for M/DN Intramedullary Nail System

    Zimmer, Inc. is recalling 4.5mm Cortical Screws for the M/DN system because they are not compatible with the device, potentially causing surgical complications.

    Product
    Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail System, Orthopedic surgical device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1702-2015·2015-06-10

    Alcon Custom Pak Recalled for Potential Glove Splits and Holes

    Alcon Research, Ltd. is recalling Alcon Custom Paks because the Devon Light Glove component may have splits or holes, which could lead to surgical site infections.

    Product
    The Alcon Custom Pak. The Alcon Customer Pak is an assemblage of single-use medical devices and accessories designed by medical professionals for specific ophthalmic surgical procedures. Some Paks contain the Devon Light Glove.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15C002000·2015-06-10

    Baby Jogger Recalls Infant Car Seats Due to Labeling Errors

    Baby Jogger is recalling specific infant car seats because labels and manuals contain incorrect or missing safety information, which may increase injury risk in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1113-2015·2015-06-10

    Sucrets Cherry Lozenges Recalled for Incorrect Labeling

    Medtech Products is recalling Sucrets Sore Throat & Cough Vapor Cherry lozenges because an incorrect book label was applied to the tins.

    Product
    SUCRETS Sore Throat & Cough Vapor Cherry lozenges, 18-count tin, Dist. By: Insight Pharmaceuticals, LLC, Trevose, PA 19053-8433
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1700-2015·2015-06-10

    Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Heparin Activity Failure

    Edwards Lifesciences is recalling 978 Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters because they failed internal statistical tests for heparin activity.

    Product
    Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters model number 744HF75. Flow-directed pulmonary artery catheters for monitoring cardiac output, mixed venous oxygen saturation, and end diastolic volume when used with the Vigilance Monitor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1111-2015·2015-06-10

    Mylan Recalls Mycophenolic Acid Tablets for Dissolution Failures

    Mylan Pharmaceuticals is recalling 7,722 bottles of Mycophenolic Acid Delayed-release Tablets, 180 mg, because they failed to meet dissolution specifications.

    Product
    Mycophenolic Acid Delayed-release Tablets, 180 mg, 120-count bottle, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A., NDC 0378-4201-78, UPC 3 0378-4201-78 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1708-2015·2015-06-10

    Siemens Dimension Vista LOCI TSH Test Recalled for Inaccurate Results

    Siemens is recalling 2,256 units of the Dimension Vista LOCI TSH test due to a defect that may cause falsely low results.

    Product
    Dimension Vista Systems LOCI Thyroid Stimulating Hormone; the TSH method is an in vitro diagnostic test for the quantitative measurement of Thyroid Stimulating Hormone in human serum and plasma on the Dimension Vista System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1705-2015·2015-06-10

    Siemens Medical Software Recall for Missing Image Measurements on Printouts

    Siemens Medical Solutions is recalling 167 units of Syngo.via and Syngo.x software because measurements on subsequent images do not appear on printouts.

    Product
    Syngo.via and Syngo.x ; a software solution intended to be used for viewing, manipulation, communication, and storage of medical images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1112-2015·2015-06-10

    Teva Recalls Zebeta Tablets Due to Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling 889 bottles of Zebeta (bisoprolol fumarate) 10mg tablets because they failed dissolution specifications during stability testing.

    Product
    Zebeta¿ (bisoprolol fumarate), tablets, 10mg, 30-count bottle, Rx only, Manufactured for Teva Pharmaceuticals Inc. 425 Privet Road, Horsham, PA by Duramed Pharmaceuticals, Inc., a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY 10970 for Teva. NDC 51285-061-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1114-2015·2015-06-10

    Fresenius Kabi Recalls KABIVEN IV Bags Due to Amino Acid Labeling Error

    Fresenius Kabi is recalling 5,488 bags of KABIVEN IV solution because the label lists 3.1% amino acids, but the product actually contains 3.3%.

    Product
    KABIVEN — KABIVEN (DEXTROSE, SOYBEAN OIL, ELECTROLYTES, LYSINE, PHENYLALANINE, LEUCINE, VALINE, THREONINE, METHIONINE, ISOLEUCINE, TRYPTOPHAN, ALANINE, ARGININE, GLYCINE, PROLINE, HISTIDINE, GLUTAMIC ACID, SERINE, ASPARTIC ACID AND TYROSINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1115-2015·2015-06-10

    Sandoz Recalls Cetirizine HCl Chewable Tablets Due to Impurity Failure

    Sandoz, Inc. is recalling specific lots of Cetirizine HCl Chewable Tablets because an impurity exceeded specifications during stability testing.

    Product
    Cetirizine HCl Chewable Tablet, 10 mg, 6-tablets in one blister, in 12 (2 blisters) and 24 (4 blisters) tablet count configurations. Manufactured by Sandoz Private Limited Village-Digham Opp. Thane-Belapur Road Navi Mumbai, 400 078, India, for Sandoz Private Limited 100 College…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1707-2015·2015-06-10

    Ortho-Clinical Diagnostics Recalls VITROS Signal Reagent Due to Labeling Defects

    Ortho-Clinical Diagnostics is recalling VITROS Immunodiagnostic Products Signal Reagent, Lot 3082, because the reagent packs may contain blank labels.

    Product
    VITROS Immunodiagnostic Products Signal Reagent, Product Code 1072693, Unique Device Identifier No. 10758750008360 VITROS Immunodiagnostics Products Signal Reagent (SR) is supplied to users as a sales unit box containing two Signal Reagent Packs. Each Signal Reagent Pack is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V358000·2015-06-09

    GM Recalls 2015 Cadillac ATS and CTS for Brake Pedal Bracket Fracture

    General Motors is recalling 2015 Cadillac ATS and CTS vehicles because a brake pedal bracket may fracture, preventing the driver from applying the brakes.

    Product
    CADILLAC — CADILLAC CTS, ATS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V359000·2015-06-09

    Forest River Recalls 2016 Trailers Due to Wheel Stud Failure Risk

    Forest River is recalling 1,497 model year 2016 trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER SHOCKWAVE, STEALTH, VIBE, CHEROKEE GREY WOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V357000·2015-06-09

    Kalmar Ottawa T2 Tractors Recalled for Engine Fire Risk

    Kalmar is recalling 2010-2014 Ottawa T2 tractors because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V356000·2015-06-09

    Gulf Stream Recalls 2015 Trailers Due to Failing Entry Step Rivets

    Gulf Stream is recalling 2015 Canyon Trail and Sedona trailers because entry step rivets may shear, causing steps to fail and increasing the risk of falls.

    Product
    GULF STREAM — GULF STREAM CANYON TRAIL, SEDONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V355000·2015-06-09

    Vermeer Recalls 2015 TLR30HD and TLR30LD Trailers for Safety Chain Defect

    Vermeer is recalling specific 2015 TLR30HD and TLR30LD trailers because an incorrectly installed safety chain may fail to prevent the trailer from separating from the tow vehicle.

    Product
    VERMEER — VERMEER TLR30HD, TLR30LD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V351000·2015-06-08

    Mercedes-Benz Recalls 2015 E250, GLK250, and ML250 for Oil Leak Fire Risk

    Mercedes-Benz is recalling specific 2015 E250, GLK250, and ML250 vehicles because oil may leak from the chain tensioner gasket, creating a fire hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E250, GLK250, ML250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V352000·2015-06-08

    Fontaine Recalls 2016 Revolution Trailers Due to Washer Cracking Risk

    Fontaine is recalling 2016 Revolution semi-trailers because hardened washers may crack, potentially causing structural detachment and increasing crash risk.

    Product
    FONTAINE — FONTAINE REVOLUTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V349000·2015-06-05

    Prevost Recalls 2006-2010 X3-45 Coaches Due to Fire Risk

    Prevost is recalling 314 X3-45 coaches from 2006-2010 because rusted booster studs may break, allowing power cables to short against the frame and cause a fire.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide