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.

54601–54625 of 74002

  • ModerateFDA (Drugs)·D-929-2015·2015-04-29

    Attix Pharmaceuticals Recalls Ticarcillin Sodium/Potassium Clavulanate API Due to Stability Data Issues

    Attix Pharmaceuticals is recalling Ticarcillin Sodium/Potassium Clavulanate API because stability data does not support the printed expiry dates for lots distributed between 2012 and 2015.

    Product
    Ticarcillin Sodium/Potassium Clavulanate (30:1) active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-968-2015·2015-04-29

    Tarmac Recalls Well at Walgreens Antacid Liquid for Failed Antimicrobial Test

    Tarmac Products, Inc. is recalling Well at Walgreens Regular Strength Antacid Liquid because the product failed the Antimicrobial Effectiveness Test.

    Product
    Well at Walgreens Regular Strength Antacid Liquid, Mint Flavor 12 FL OZ (355 mL) bottle
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1479-2015·2015-04-29

    SpineFrontier Recalls MISquito Pedicle Screw System Surgical Technique Document

    SpineFrontier is recalling the MISquito Pedicle Screw System Surgical Technique document because it does not adequately convey the intended use of the Rod Caliper.

    Product
    SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique; Part Number: DOC80023. The Rod Caliper is a manual surgical instrument that may be used as part of the PedFuse Pedicle Screw System and its MISquito components during percutaneous, minimally…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-966-2015·2015-04-29

    Tarmac Recalls Well at Walgreens Comfort Gel for Antimicrobial Failure

    Tarmac Products, Inc. is recalling 41,743 bottles of Well at Walgreens Maximum Strength Comfort Gel because the product failed the Antimicrobial Effectiveness Test.

    Product
    Well at Walgreens Maximum Strength Comfort Gel 12 FL OZ (355 mL) bottle,
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0962-2015·2015-04-29

    Nomax Recalls GLOSTRIPS Ophthalmic Strips for Packaging Degradation

    Nomax Inc. is recalling GLOSTRIPS ophthalmic strips because packaging degradation may affect the uniformity of the rose bengal dosage.

    Product
    GLOSTRIPS — GLOSTRIPS (ROSE BENGAL SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0963-2015·2015-04-29

    Nomax Recalls Fluorescein Sodium Ophthalmic Strips for Content Uniformity Issues

    Nomax Inc is recalling Fluorescein Sodium Ophthalmic Strips because packaging degradation may affect dosage uniformity. The recall covers 62,691 cartons distributed in the US and internationally.

    Product
    Fluorescein Sodium Ophthalmic Strips USP, 1.0 mg per strip, labeled as 1) FUL-GLO, individually wrapped strips, barcode (01)00317478404019; packaged in 100-count strips per carton, (NDC 17478-404-01), UPC 3 17478 40401 9, Manufactured for: Akorn, Inc., Lake Forest, IL 60045.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0964-2015·2015-04-29

    Mucinex DM Recalled for Defective Pouch Seal

    Reckitt Benckiser is recalling Mucinex DM extended-release tablets due to a defective seal on the top of the pouch.

    Product
    MUCINEX DM — MUCINEX DM (GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V253000·2015-04-28

    Mastercraft Recalls 2015 Boat Trailers Due to Tongue Bolt Failure Risk

    Mastercraft is recalling 1,740 model year 2015 boat trailers because the tongue bolt may fail, allowing the trailer to disconnect from the tow vehicle and increasing crash risk.

    Product
    MASTERCRAFT — MASTERCRAFT BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V249000·2015-04-28

    Spartan Recalls 2014 Utilitmaster Walk-In Vans for Driveshaft Defect

    Spartan Motors is recalling 97 model year 2014 Utilitmaster Walk-In Vans because inadequately torqued fasteners may cause the driveshaft to disconnect, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V251000·2015-04-28

    Ford Recalls 2015 F-150 Trucks for Missing Underbody Heat Shields

    Ford is recalling 2015 F-150 vehicles manufactured in late January 2015 because loose or missing underbody heat shields can cause fuel line degradation and increase fire risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V250000·2015-04-28

    Ford Recalls 2013-2015 Fusion, MKZ, and Edge for Steering Bolt Corrosion

    Ford is recalling specific 2013-2015 Fusion, Lincoln MKZ, and 2015 Edge vehicles because road salt may corrode steering bolts, potentially causing a loss of power steering assist.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·070-2015·2015-04-27

    Skyline Provisions Recalls Beef Products Due To E. Coli O157:H7 Contamination

    Skyline Provisions is recalling 1,029 pounds of beef products contaminated with E. coli O157:H7. The recall was announced by the USDA Food Safety and Inspection Service.

    Product
    Skyline Provisions — Skyline Provisions, Inc., Recalls Beef Products Due To E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V247000·2015-04-27

    Spartan Recalls Utilimaster Vans Due to Reversed Backup Camera Images

    Spartan Motors is recalling 2012-2015 Utilimaster Walk-in vans and truck bodies because the backup camera may display reversed images, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER TRUCK BODY, WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V248000·2015-04-27

    Ford Recalls 2015 Lincoln MKZ for Excessive Parking Light Output

    Ford is recalling 21,435 2015 Lincoln MKZ vehicles because parking lights may not dim correctly when headlights are on, potentially blinding oncoming traffic.

    Product
    LINCOLN — LINCOLN MKZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V246000·2015-04-24

    Ford Recalls Fiesta, Fusion, and MKZ Vehicles for Door Latch Defect

    Ford is recalling specific 2011-2014 Fiesta, Fusion, and MKZ vehicles because a door latch component may break, potentially allowing doors to open while driving.

    Product
    FORD — FORD, LINCOLN FIESTA, MKZ, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1948-2015·2015-04-22

    Cost Plus Recalls Ceramic Spoons for Lead and Cadmium Levels

    Cost Plus Management Services is recalling 15,700 Shanghai Ceramic Spoons because they may exceed FDA guidance levels for leachable lead and cadmium.

    Product
    Shanghai Ceramic Spoons; SKU 487874; UPC 2487874
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V241000·2015-04-22

    Navistar Recalls 2011-2015 Commercial Vehicles for HVAC Fire Risk

    Navistar is recalling 82,736 commercial vehicles because an electrical issue in the HVAC system could cause a fire.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS TERRASTAR, AC, TRANSTAR, HC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1943-2015·2015-04-22

    Trader Joe's Cinnamon Almonds Recalled for Undeclared Peanuts

    Trader Joe's is recalling 16-ounce packages of Cinnamon Almonds because they may contain undeclared peanuts.

    Product
    Cinnamon Almonds, Net Wt. 16 oz, UPC # 00761437, 24 units per case
    Category
    Food
    Distribution
    Distributed nationwide