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.

58801–58825 of 74011

  • SevereFDA (Drugs)·D-1210-2014·2014-04-16

    Terra-Medica Recalls Pleo Ex Drops Due to Penicillin Cross Contamination

    Terra-Medica Inc. is recalling Pleo Ex DROPS 5X homeopathic antifungal medicine due to penicillin cross-contamination. The product was distributed in the US, Canada, the Philippines, and online.

    Product
    Pleo Ex DROPS 5X, 10 ml bottles, Homeopathic Antifungal Medicine, OTC Only. Made in Germany for: SANUM USA Corp., 1465 Slater Road, Ferndale, WA 98248 by Sanum-Kehlbeck GMbH & Co. KG. NDC: 49807-1003-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1448-2014·2014-04-16

    Pega Medical Recalls Fassier-Duval Intramedullary Rods Due to Material Defect

    Pega Medical Inc. is recalling five units of the Fassier-Duval IM Telescopic System because the male components were made with material of lower strength than specifications.

    Product
    Pega Medical Inc., Fassier-Duval IM Telescopic System, male component (solid shaft), Part number: M040-SS-110; Used in Implant Catalogue number: FD-040(LS)-SS. orthopedic intramedullary rod.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1195-2014·2014-04-16

    Terra-Medica Recalls Pleo Not DROPS Due to Penicillin Cross Contamination

    Terra-Medica Inc. is recalling specific batches of Pleo Not DROPS homeopathic medicine due to penicillin cross contamination. The product was distributed in the US, Canada, and the Philippines.

    Product
    Pleo Not DROPS, 5X, 10 mL Bottles, Oral Homeopathic Medicine, OTC Only. Made in Germany, Distributed by: SANUM USA Corp.,1465 Slater Road, Fernadale, WA 98248; Manufactured By: SANUM-Kehlbeck GmbH & Co. KG. NDC: 49807-2301-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1196-2014·2014-04-16

    Terra-Medica Recalls Pleo Not Portable Sips Due to Penicillin Contamination

    Terra-Medica Inc. is recalling Pleo Not Portable Sips oral homeopathic medicine due to penicillin cross-contamination. The products were distributed in the US, Canada, and the Philippines.

    Product
    Pleo Not PORTABLE SIPS, 5X, 10 x 1mL Cartons, Oral Homeopathic Medicine, OTC Only. Made in Germany, Distributed by: SANUM USA Corp.,1465 Slater Road, Fernadale, WA 98248; Manufactured By: SANUM-Kehlbeck GmbH & Co. KG. NDC: 49807-2306-1. Pleo Not PORTABLE SIPS, 5X, 50 x 1mL…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1211-2014·2014-04-16

    Terra-Medica Recalls Pleo Ex Portable Sips Due to Penicillin Contamination

    Terra-Medica Inc. is recalling specific batches of Pleo Ex Portable Sips homeopathic medicine due to penicillin cross-contamination.

    Product
    Pleo Ex PORTABLE SIPS 5X, 10 x 1 mL, Oral Homeopathic Medicine, OTC Only. Made in Germany. Distributed by: SANUM USA Corp. 1465 Slator Road, Ferndale, WA 98248. Manufactured by: Sanum-Kehlbeck GmbH & Co. KG, NDC: 49807-1005-1. PLEO--EX Portable Sips 5X, 50 x 1 mL, Oral…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1229-2014·2014-04-16

    Glenmark Recalls Ranitidine Tablets Due to Foreign Metoprolol Contamination

    Glenmark Generics Inc. is recalling specific bottles of Ranitidine Tablets USP 150 mg because they were found to contain foreign Metoprolol Tartrate tablets.

    Product
    Ranitidine Tablets USP, 150 mg, 500-count bottles, Rx only, Manufactured by: Shasun Pharmaceuticals Limited, Unit-II R.S. No 32 33 & 34, Shasun Road, Periyakalapet, Puducherry, - 605 014, India; Manufactured for: Glenmark Generics Inc, USA, Mahwah, NJ 07430, UPC 3 68462 24805 8…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1208-2014·2014-04-16

    Terra-Medica Recalls Pleo Fort Tablets Due to Penicillin Cross Contamination

    Terra-Medica Inc. is recalling Pleo Fort Tablets 5X due to penicillin cross-contamination. The product was distributed nationwide and internationally.

    Product
    Pleo Fort TABLETS 5X, 20 Tablet Carton, Homeopathic Digestive Aid Medicine, OTC Only. Made in Germany. Distributed by: SANUM USA Corp., 1465 Slater Road, Ferndale WA 98248. Manufactured by: Sanum-Kehlbeck GmbH & Co. KG. NDC: 49807-1102-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1200-2014·2014-04-16

    Terra-Medica Recalls Pleo Quent Suppositories Due to Penicillin Contamination

    Terra-Medica Inc. is recalling Pleo Quent Suppositories 3X due to penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.

    Product
    Pleo Quent SUPPOSITORIES 3X, 10 Suppository Cartons, Oral Homeopathic Medicine, OTC Only. Made in Germany for: SANUM USA Copr, 1456 Slater Road, Ferndale, WA 98248 by Sanum-Kehlbeck GmbH & Co. KG. NDC: 49807-2904-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1199-2014·2014-04-16

    Terra-Medica Recalls Pleo Nota-Quent Drops Due to Penicillin Contamination

    Terra-Medica Inc. is recalling Pleo Nota-Quent Drops because of penicillin cross-contamination. The product is distributed in the US, Canada, and the Philippines.

    Product
    Pleo Nota- Quent DROPS 5X, 10 mL Bottles, Homeopathic Medicine, OTC Only. Made in Germany, Manufactured by: Sanum-Kehlbeck GmbH & Co. KG, Hoya, Germany. Distributed by: SANUM USA Corp., 1465 Slater Road, Ferndale, WA 98248. NDC: 49807-0031-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1197-2014·2014-04-16

    Terra-Medica Recalls Pleo Not Portable Sips Due to Penicillin Contamination

    Terra-Medica Inc. is recalling specific batches of Pleo Not Portable Sips oral homeopathic medicine because of penicillin cross-contamination.

    Product
    Pleo Not PORTABLE SIPS, 6X, 10 x 1mL Cartons, Oral Homeopathic Medicine, OTC Only. Made in Germany, Distributed by: SANUM USA Corp.,1465 Slater Road, Fernadale, WA 98248; Manufactured By: SANUM-Kehlbeck GmbH & Co. KG. NDC: 49807-2308-1. Pleo Not PORTABLE SIPS, 6X, 50 x 1mL…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1440-2014·2014-04-16

    Draeger Oxylog 3000 Plus Ventilators Recalled Due to Potentiometer Fault

    Draeger Medical Systems is recalling three Oxylog 3000 plus ventilators because the control knobs may interrupt contact, causing the device to stop ventilation.

    Product
    Draeger Oxylog 3000 plus ventilators, emergency and transport ventilator. Part number: 5704833
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14730·2014-04-16

    GunBox Recalls Gun Storage Boxes Due to Locking Mechanism Failure

    The GunBox LLC is recalling about 1,000 gun storage boxes because the locking mechanism can open if dropped, allowing access to the gun inside.

    Product
    The GunBox™ Gun Storage Boxes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1750-2014·2014-04-16

    Keen-Wah Quinoa Clusters Recalled for Undeclared Soy Allergen

    Keen-Wah LLC is recalling i heart keenwah Almond All Natural Quinoa Clusters because soy lecithin was used in manufacturing but not declared on the label.

    Product
    i heart keenwah Almond All Natural Quinoa Clusters. UPC 736211802347 for the 4 oz UPC 713757598200 for the 1 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1749-2014·2014-04-16

    Keen-Wah Quinoa Clusters Recalled for Undeclared Soy Allergen

    Keen-Wah LLC is recalling i heart keenwah Chocolate Sea Salt All Natural Quinoa Clusters because soy was not declared on the label.

    Product
    i heart keenwah Chocolate Sea Salt All Natural Quinoa Clusters. UPC 736211802446 for the 4 oz UPC 713757598101 for the 1 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1438-2014·2014-04-16

    Philips HeartStart XL+ Defibrillator Recall for Software Communication Failure

    Philips is recalling HeartStart XL+ Defibrillators because a software failure may lock users out of clinical mode, potentially delaying therapy.

    Product
    Philips HeartStart XL+ Defibrillator/Monitor with system software version B.00.00 or B.00.01 installed Model: 861290, automatic external defibrillator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1446-2014·2014-04-16

    Breg Recalls Knee Sleeves for Missing Latex Warning Labels

    Breg Inc is recalling specific knee sleeves because they contain latex but lack the required caution labels.

    Product
    Economy Elastic Knee Sleeve Open, Model No. 121414 and 121415. Product Usage: The product is intended to provide flexible knee support.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1336-2014·2014-04-16

    Playtex Electric Breast Pump Recall Due to Power Adapter Shock Risk

    Energizer Personal Care is recalling Playtex Deluxe Double Electric Breast Pumps because loose power adapter casings may cause electric shock.

    Product
    Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120, which is included with the package.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1451-2014·2014-04-16

    Harbor Freight Recalls Sit/Stand Rolling Walkers Due to Wheel Detachment Risk

    Harbor Freight Tools is recalling Sit/Stand Rolling Walkers because wheels may detach over time, posing a hazard to users.

    Product
    Sit/stand Rolling Walker, SKU/Item Number 66838. Intended for use by those with difficulty walking and weighing 225 lbs. or less.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1209-2014·2014-04-16

    Terra-Medica Recalls Pleo Ex Suppositories Due to Penicillin Cross-Contamination

    Terra-Medica Inc. is recalling Pleo Ex Suppositories because of penicillin cross-contamination. The affected homeopathic antifungal products were distributed in the US, Canada, and the Philippines.

    Product
    Pleo Ex SUPPOSITORIES 3X, 10 Suppository Packages; Homeopathic Antifungal Medicine, OTC Only. Made in Germany. Distributed by: SANUM USA Corp., 1465 Slater Road, Ferndale, WA 98248. Manufactured by: Sanum-Kehlbeck GmbH & Co. KG. NDC: 49807-1001-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1205-2014·2014-04-16

    Terra-Medica Recalls Pleo Fort Capsules Due to Penicillin Cross Contamination

    Terra-Medica Inc. is recalling Pleo Fort Capsules 4X due to penicillin cross contamination. The product was distributed in the US, Canada, and the Philippines.

    Product
    Pleo Fort CAPSULES 4X, 20 Capsule Cartons Homeopathic Digestive Aid Medicine, OTC Only. Made in Germany for: SANUM USA Copr, 1456 Slater Road, Ferndale, WA 98248 by Sanum-Kehlbeck GmbH & Co. KG. NDC: 49807-1103-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1747-2014·2014-04-16

    Northern Valley Baking Recalls G'nache P'nache for Undeclared Milk and Soy

    Northern Valley Baking Co. is recalling G'nache P'nache products because milk and soy were not declared on the allergen statement.

    Product
    The Other Macaroon G'nache P'nache 5.3 oz. Manufactured and Distributed by:Northern Valley Baking Co LLC, Dumont, New Jersey USA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1452-2014·2014-04-16

    Draeger Recalls Reusable Latex Breathing Bags Due to Allergic Reaction Incident

    Draeger Medical is recalling reusable latex breathing bags and test lungs after a user reported an acute allergic reaction. The product is distributed nationwide.

    Product
    Reusable latex breathing bags with multiple part numbers and sold as part of test lung part number and reusable anaesthesia sets. Product Usage: The breathing bag is a component of the anesthesia set (breathing circuit) that is intended to is the conduit for administering…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1450-2014·2014-04-16

    Medcare Floor Lifts Recalled Due to Potential Pin Failure

    ErgoSafe Product LLC is recalling Medcare Floor Lifts manufactured between 2010 and 2012 because a design pin may break over time.

    Product
    400003 Medcare Lift with Scale 400013 Medcare Lift w/Scale 600 lb 400600 Scale Hanger Assembly Product Usage: The intended use is a patient hanger bar (400600) attached to a 400003 or 400013 floor lift used to lift, transfer or position clients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1752-2014·2014-04-16

    Keen-Wah Quinoa Clusters Recalled for Undeclared Soy Allergen

    Keen-Wah LLC is recalling i heart keenwah Cranberry Cashew Quinoa Clusters because soy lecithin was used in manufacturing but not declared on the label.

    Product
    i heart keenwah Cranberry Cashew All Natural Quinoa Clusters. UPC 736211802545 for the 4 oz UPC 713757598309 for the 1 oz
    Category
    Food
    Distribution
    Distributed nationwide