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.

Which agencies issued them

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.

53876–53900 of 74002

  • ModerateFDA (Drugs)·D-0997-2015·2015-05-20

    Akorn Recalls Sulfamethoxazole and Trimethoprim Oral Suspension for Dissolution Failure

    Akorn, Inc. is recalling 8,400 cups of Sulfamethoxazole and Trimethoprim oral suspension because the sulfamethoxazole failed to meet dissolution specifications.

    Product
    SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION, USP 800 mg/ 160 mg per 5mL, GRAPE FLAVOR, 20 mL unit dose cup (NDC 50383-0824-20), Rx only, HI-TECH PHARMACAL CO. INC, Amityville, NY 11701
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1065-2015·2015-05-20

    Mission Pharmacal Recalls Sodium Sulfacetamide and Sulfur Wash Kits

    Mission Pharmacal is recalling 1,992 kits of Sodium Sulfacetamide 9% and Sulfur 4.5% Wash due to microbial contamination.

    Product
    Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen, Rx Only, Sunscreen Broad Spectrum SPF 25, Net Wt. 3 oz (85 g), Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Net Wt. 16 oz (454 g), Manufactured for: BioComp Pharma Inc., San Antonio TX, 78230, NDC 44523-616-23
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1612-2015·2015-05-20

    Fujifilm Synapse Cardiovascular Software Recall for Patient Demographic Mismatch

    Fujifilm Medical Systems is recalling Synapse Cardiovascular software versions v4.0.8 and v4.0.8 SR1 because patient demographics in exported reports may not match the clinical reports.

    Product
    Fujifilm Synapse Cardiovascular I ProSolv CardioVascular Synapse Cardiovascular v4.0.8 Synapse Cardiovascular v4.0.8 SR1 Intended Use: Picture Archiving and Communication System Computer, Diagnostic, Programmable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1614-2015·2015-05-20

    Stryker Recalls 80 mm Kinemax Stem Extenders Due to Mislabeling

    Stryker Howmedica Osteonics is recalling four 80 mm Kinemax Stem Extenders because they were shipped in boxes labeled for the 80 mm part but contained 40 mm extenders.

    Product
    Kinemax Stem Extenders, 80 mm, Product Usage: Kinemax Cemented Stem Extenders are modular components designed to be mated with tibial baseplates or femoral components of the Modular Rotating Hinge (MRH), Scorpio Total Stabilizer (TS) or Duracon TS knee replacement systems.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1078-2015·2015-05-20

    Cipla Recalls Levalbuterol Inhalation Solution Vials for Impurity Failure

    Cipla Limited is recalling 140,625 vials of Levalbuterol Inhalation Solution because the product failed impurity specifications. The affected lot is distributed nationwide.

    Product
    Levalbuterol Inhalation Solution, USP, 0.31 mg/ 3 mL, 3 mL Vials, Rx Only. Manufactured by: Cipla Ltd. Plot 9 & 10, Indure, SEZ, Pithampur, M.P.-454 775, INDIA, Manufactured for: Dr. Reddy's Laboratories, Inc., Princeton NJ 08640. NDC: 43598-412-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1597-2015·2015-05-20

    Spinal Elements Mercury Lordosed Rods Recalled for Missing Traceability Markings

    Spinal Elements, Inc. is recalling 588 Mercury lordosed rods because some lack required product identification markings, interrupting device traceability.

    Product
    Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component of the Mercury Spinal System, comprised of a variety of screws, hooks, rods, connectors, and staples that are used for attachment to the non-cervical spine. Rods span the distance between screws and hooks and achieve…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1077-2015·2015-05-20

    FDA Recalls Monistat 1 Simple Cure for Missing Topical Cream

    Medtech Products, Inc. is recalling Monistat 1 Simple Cure because the distributed units lack the required topical cream.

    Product
    MONISTAT 1 COMBINATION PACK — MONISTAT 1 COMBINATION PACK (MICONAZOLE NITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1079-2015·2015-05-20

    Apotex Recalls Subpotent Olanzapine Orally Disintegrating Tablets

    Apotex Inc. is voluntarily recalling specific lots of Olanzapine 5 mg orally disintegrating tablets because they contain less active drug than labeled.

    Product
    Olanzapine, Orally Disintegrating Tablets, 5 mg, a) 30-count bottle (NDC 60505-3275-03), b) 100-count blister (NDC 60505-3275-00), Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1081-2015·2015-05-20

    Apotex Recalls Subpotent Olanzapine Orally Disintegrating Tablets

    Apotex Inc. is voluntarily recalling 5,352 bottles of Olanzapine 20 mg tablets because the drug was found to be subpotent.

    Product
    Olanzapine, Orally Disintegrating Tablets, 20 mg, 30-count bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V294000·2015-05-19

    Blue Bird All American Buses Recalled for Engine Fire Risk

    Blue Bird is recalling 2009-2016 All American non-school buses due to a defect that may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V296000·2015-05-19

    NABI Transit Bus Recall for Engine Vent Tube Fire Risk

    NABI is recalling 2007-2015 LFW, BRT, and 2007-2013 CLFW transit buses because a vent tube may detach, allowing engine oil to contact hot surfaces and cause a fire.

    Product
    NABI — NABI LFW, CLFW, BRT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15138·2015-05-19

    Precision Trading Recalls Espresso Makers Due to Burn Risk

    Precision Trading is recalling about 4,700 PREMIUM Espresso Makers because the filler cap can crack or pop off, releasing steam and posing a burn risk.

    Product
    PREMIUM® Espresso Makers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15139·2015-05-19

    Kaldi's Coffee Recalls Disposable Cup Sleeves Due to Fire Hazard

    Kaldi's Coffee Roasting is recalling about 700,000 disposable paper cup sleeves because they can ignite in microwaves. Two fire incidents were reported, with no injuries.

    Product
    Disposable Cup Sleeves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V295000·2015-05-19

    Gillig Low Floor Bus Taillight Bracket Recall

    Gillig is recalling 2014-2015 Low Floor buses because taillight brackets may detach, reducing visibility and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·15E040000·2015-05-18

    Takata Frontal Driver Air Bag Inflator Module Recall

    Takata is recalling specific frontal driver air bag inflator modules that may rupture during deployment, potentially causing serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E042000·2015-05-18

    Takata Passenger Air Bag Inflator Recall for Honda, Toyota, Pontiac, Subaru

    Takata is recalling PSPI-L passenger air bag inflators in specific Honda, Toyota, Pontiac, and Subaru models. The inflators may rupture in a crash, sending metal fragments into the vehicle.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V290000·2015-05-18

    RAM 4500 and 5500 Trucks Recalled for Tire Speed Rating Mismatch

    Chrysler is recalling 2014-2015 RAM 4500 and 5500 trucks because their tires are rated for a lower speed than the vehicle's maximum capability, posing a crash risk.

    Product
    RAM — RAM 4500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E041000·2015-05-18

    Takata Passenger Air Bag Inflator Recall for 2001-2008 Vehicles

    Takata is recalling specific passenger frontal air bag inflators for 2001-2008 vehicles due to a risk of rupture during deployment.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V292000·2015-05-18

    New Flyer Buses Recalled for Engine Vent Tube Fire Risk

    New Flyer is recalling certain 2008-2014 buses because a vent tube may detach, allowing engine oil to contact hot surfaces and increase fire risk.

    Product
    NEW FLYER — NEW FLYER C40LF, C40LFR, C35LF, C35LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide