The Recall Desk

State

US Virgin Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51676–51700 of 73995

  • LowFDA (Drugs)·D-0022-2016·2015-10-21

    Loratadine Tablets Recalled for Out-of-Specification Assay Results

    Ohm Laboratories is recalling CareOne Loratadine tablets because they failed potency testing. Consumers should stop using the affected products.

    Product
    CareOne Original Prescription Strength, Allergy Relief, Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box, NDC 41520-525-69, UPC 3 41520 31346 2; b) Children's 10-count tablets per box NDC 41520-527-69, UPC 3 41520 31455 1; Distributed…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0035-2016·2015-10-21

    TopCare Loratadine Tablets Recalled for Out-of-Specification Assay Results

    Ohm Laboratories is recalling TopCare Loratadine tablets because they failed potency testing. Consumers should stop using the affected products.

    Product
    TopCare LORATIDINE ORALLY DISINTEGRATING TABLETS, , USP, 10 mg, packaged in a) Children's 10-count tablets per box (NDC 36800-528-69, UPC 0 3680010261 3); and b) 10-count tablets per box, (NDC 36800-527-69, UPC 0 3680008395 0); Distributed by Topco Associates, LLC, Elk Grove…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0023-2016·2015-10-21

    CVS Loratadine Tablets Recalled for Out-of-Specification Assay Results

    CVS Pharmacy loratadine tablets are being recalled because they failed potency testing. Consumers should stop using the product and return it to the pharmacy.

    Product
    CVS Pharmacy, Original Prescription Strength, LORATADINE ORALLY DISINTEGRATING TABLETS, USP, 10 mg, packaged in a) 10-count tablets per box, Item 876239, UPC 0 50428 61152 4, and b) 30-count tablets per box, Item 367404, UPC 0 50428 11367 7, Distributed by: CVS Pharmacy, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0026-2016·2015-10-21

    Fred's Loratadine Tablets Recalled for Out-of-Specification Assay Results

    Ohm Laboratories is recalling Fred's Loratadine Orally Disintegrating Tablets due to an out-of-specification assay result. The FDA classifies this as a Class III recall.

    Product
    Fred's Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-counts tablets per box, Distributed by: fred's, Inc., 4300 New Getwell Road, Memphis, TN 38118, UPC 0 8457912198 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0037-2016·2015-10-21

    Sunmark Loratadine Tablets Recalled for Out-of-Specification Assay Results

    Ohm Laboratories is recalling Sunmark loratadine tablets because they failed potency testing. Consumers should stop using the affected products.

    Product
    Sunmark loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box (NDC 49348-930-01, UPC 0 1093936544 6); and b) 30-count tablets per box (NDC 49348-930-44, UPC 0 1093934944 6) Distributed by McKesson, One Post Street, San Francisco, CA…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0016-2016·2015-10-21

    Tribute Pharmaceuticals Recalls Fenofibric Acid Tablets Due to Benzophenone Contamination

    Tribute Pharmaceuticals is recalling specific lots of Fenofibric Acid Tablets because they may contain trace amounts of benzophenone from label varnish.

    Product
    Fenofibric Acid Tablets, 35 mg, 30-count bottles, labeled as a) FIBRICOR (fenofibric acid) Tablets, NDC 13310-101-07, UPC 3 13310-101-07 8, Manufactured for: AR SCIENTIFIC, INC., Philadelphia, PA 19124 USA; by: MUTUAL PHARMACEUTICAL CO., INC., Philadelphia, PA 19124 USA; b)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0020-2016·2015-10-21

    Rite Aid Loratadine Tablets Recalled for Out-of-Specification Assay

    Ohm Laboratories is recalling Rite Aid Pharmacy loratadine orally disintegrating tablets because they failed an assay test, resulting in a superpotent drug classification.

    Product
    Rite Aid Pharmacy loratadine orally disintegrating tablets USP, 10 mg, packaged in a) 30-count tablets per box, Item 352712, UPC 0 11822 52712 5; b) 60-count tablets per box, Item 353672, UPC 0 11822 53672 1. Distributed By: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0017-2016·2015-10-21

    Tribute Pharmaceuticals Recalls Fenofibric Acid Tablets Due to Benzophenone Contamination

    Tribute Pharmaceuticals is recalling 140,607 bottles of Fenofibric Acid Tablets 105 mg because they may contain trace amounts of benzophenone from label varnish.

    Product
    Fenofibric Acid Tablets 105 mg, Rx only, labeled as a) FIBRICOR (fenofibric acid) Tablets, 30-count bottles, NDC 13310-102-07, UPC 3 13310-102-07 5; b) FIBRICOR (fenofibric acid) Tablets, 90-count bottles, NDC 13310-102-90, UPC 3 13310-102-90 7; Manufactured for: AR SCIENTIFIC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0031-2016·2015-10-21

    Major Loratadine Tablets Recalled for Out-of-Specification Assay Results

    Ohm Laboratories is recalling Major loratadine orally disintegrating tablets due to out-of-specification assay results. The recall covers 29,360 boxes distributed nationwide.

    Product
    Major loratadine orally disintegrating tablets, USP, 10 mg, 10-count tablets per box, Distributed by Major Pharmaceuticals 31778 Enterprise Drive, Livonia, MI 48150, USA, NDC 0904-5806-15, UPC 3 0904580615 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0021-2016·2015-10-21

    Ohm Laboratories Recalls Loratadine Tablets Due to Assay Failure

    Ohm Laboratories is recalling specific batches of loratadine tablets because they failed potency testing. Consumers should stop using the affected products.

    Product
    Health Best Choice Care, Loratadine Orally Disintegrating Tablets, USP, 10 mg, 10-count tablets per box, Proudly Distributed by: Valu Merchandisers, Co., Kansas City, MO 64111; UPC 0 7003861209 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0038-2016·2015-10-21

    Ohm Laboratories Recalls Loratadine Tablets Due to Potency Issues

    Ohm Laboratories is recalling Wal-itin Loratadine Orally Disintegrating Tablets because they failed potency testing. The FDA classified this as a Class III recall.

    Product
    Wal-itin Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-coiunt tablets per box, (NDC 0363-0527-69, ITEM 367492,UPC 3 1191717021 3); and b) 30-count tablets per box, (NDC 0363-0527-31, ITEM 254166, UPC 3 191715562 ) Distributed by Walgreen Co., 200 Wilmot…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0034-2016·2015-10-21

    Safeway Care Loratadine Tablets Recalled for Out-of-Specification Assay

    Ohm Laboratories is recalling Safeway Care Loratadine Orally Disintegrating Tablets because they failed potency testing. Consumers should stop using the affected products.

    Product
    Safeway Care Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box (NDC 21130-527-69, UPC 3 2113076240 9); b) 30-count tablets per box (NDC 21130-527-31, UPC 3 2113076252 2) Distributed by Safeway Inc. PO BOX 99, Pleasanton, CA 94566
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V682000·2015-10-20

    Volvo Recalls 2016 VN Trucks for Transmission Locking Hazard

    Volvo is recalling 2016 VN trucks because the manual transmission may lock or cause the vehicle to move unexpectedly, increasing crash risk.

    Product
    VOLVO — VOLVO VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16013·2015-10-20

    API Outdoors Recalls Climbing Tree Stands Due to Fall Hazard

    Global Manufacturing Company is recalling API Outdoors climbing tree stands because the cable assembly can release, posing a fall hazard.

    Product
    Climbing tree stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E085000·2015-10-20

    Cummins Westport ISL G Engine Recall for Turbocharger Oil Leak Risk

    Cummins is recalling Westport ISL G engines due to a turbocharger oil supply line that may leak, increasing the risk of fire near the exhaust manifold.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:OTHER FUEL TYPES:TURBO/SUPERCHARGER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16010·2015-10-20

    Turtle Beach Recalls XO FOUR Stealth Gaming Headsets Due to Mold Risk

    Turtle Beach is recalling about 59,500 XO FOUR Stealth gaming headsets because mold spores were found on the units, posing a risk of respiratory or other infections.

    Product
    Ear Force® XO FOUR Stealth gaming headset
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16012·2015-10-20

    Big Game Recalls Climbing Tree Stands Due to Fall Hazard

    Big Game is recalling about 12,200 climbing tree stands because the cable assembly can release, posing a fall hazard. One injury report has been received.

    Product
    Climbing tree stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V681000·2015-10-20

    Nissan and Infiniti Recall Vehicles Due to Passenger Air Bag Defect

    Nissan is recalling specific 2013-2015 models because a faulty sensor may prevent the passenger air bag from deploying in a crash.

    Product
    INFINITI — INFINITI, NISSAN QX60, PATHFINDER, JX35, ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V675000·2015-10-19

    Dodge Journey Recall: Water Ingress Disables ABS and ESC Systems

    Chrysler is recalling 2012-2015 Dodge Journey vehicles because water may enter the ABS module, disabling safety systems and increasing crash risk.

    Product
    DODGE — DODGE JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V674000·2015-10-19

    Mazda Recalls 1989-1998 Vehicles for Ignition Switch Fire Risk

    Mazda is recalling approximately 1.37 million vehicles from 1989-1998 because grease in the ignition switch may overheat and cause a fire. Owners should contact a dealer for a free replacement.

    Product
    MAZDA — MAZDA 323, MX3, 626, 929
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V673000·2015-10-19

    Chrysler Recalls Jeep Vehicles for Inadvertent Air Bag Deployment Risk

    Chrysler is recalling specific 2003 Jeep Liberty and 2004 Jeep Grand Cherokee vehicles because an electrical issue may cause air bags to deploy unexpectedly, increasing injury risk.

    Product
    JEEP — JEEP LIBERTY, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide