The Recall Desk

State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56201–56225 of 74005

  • ModerateFDA (Devices)·Z-0484-2015·2014-12-03

    CooperSurgical LEEP Loop Electrode Recalled for Outer Box Mislabeling

    CooperSurgical is recalling LEEP Radius Loop Electrodes because the outer box is mislabeled with the wrong part number.

    Product
    CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D, 12 cm shaft ). Box of 5 Model Number(s): R2010 Intended Use: Diagnosis and treatment of non-invasive HPV-related or unrelated lesions of the lower genital tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0465-2015·2014-12-03

    Remel Recalls Legionella Pneumo Groups 2-14 Latex Test Kits

    Remel Inc is recalling specific lots of the Oxoid Legionella Pneumo Groups 2-14 Latex Test because a reagent may produce false negative results.

    Product
    Oxoid Legionella Pneumo Groups 2-14 Latex Test, DR0802M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, Lot 1301912. The product is a latex agglutination test for the identification of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0424-2015·2014-12-03

    Zimmer Recalls Trabecular Metal Tibial Impactor Replacement Pads

    Zimmer, Inc. is recalling 4,961 Trabecular Metal Tibial Impactor Replacement Pads due to complaints of pad fracture. The recall provides clarifying instructions for assembly and disassembly.

    Product
    Trabecular Metal Tibial Impactor Replacement Pads. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial Impactor to impact the tibial tray onto the tibia.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0423-2015·2014-12-03

    Zimmer Recalls Trabecular Metal Tibial Impactor Pads Due to Fracture Complaints

    Zimmer, Inc. is recalling Trabecular Metal Tibial Impactor Pads to provide clarifying instructions on assembly and disassembly following complaints of pad fracture.

    Product
    Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial Impactor to impact the tibial tray onto the tibia.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0256-2015·2014-12-03

    Baxter Recalls Potassium Chloride Injection Bags Due to Labeling Error

    Baxter Healthcare is recalling 63,360 bags of Potassium Chloride Injection due to incorrect outer packaging labels indicating a higher strength.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2145-2014·2014-12-03

    Market-Tiers recalls laparoscopic morcellator instructions with missing safety pages

    Market-Tiers Inc. is recalling 100 units of the blue endo MOREsolution Electromechanical Laparoscopic Morcellator System because the Instructions for Use omitted critical safety pages.

    Product
    Instructions for Use for the blue endo MOREsolution Electromechanical Laparoscopic Morcellator System, Model 55-000011, consisting of the control unit, hand-grip, flexible shaft, trocars/obturators, sleeves, valves, and blades.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0258-2015·2014-12-03

    Actavis Recalls Diclofenac Sodium and Misoprostol Tablets Due to Split Tablets

    Actavis Laboratories is recalling 5,451 bottles of Diclofenac Sodium and Misoprostol tablets because some contain split or broken tablets.

    Product
    DICLOFENAC SODIUM AND MISOPROSTOL — DICLOFENAC SODIUM AND MISOPROSTOL (DICLOFENAC SODIUM AND MISOPROSTOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0466-2015·2014-12-03

    Remel Recalls Oxoid Legionella Latex Test Due to False Negative Results

    Remel Inc is recalling Oxoid Legionella Latex Test kits because a reagent may produce false negative results. The recall covers 59 boxes distributed nationwide.

    Product
    Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Latex Reagent, DR0802, Lot 1301912. The responsible firm on the label is Oxoid Ltd.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0420-2015·2014-12-03

    Siemens Hemoglobin A1c Reagent Cartridges Recalled for Positive Bias

    Siemens is recalling certain lots of Dimension HB1C Flex reagent cartridges because they show a positive bias in hemoglobin A1c measurements.

    Product
    Siemens Dimension HB1C Flex reagent cartridge; Dimension Hemoglobin A1c (HB1C) Flex reagent cartridge on the Dimension clinical chemistry system is an in vitro diagnostic assay for the quantitative determination of hemoglobin A1c (HbA1c) in human anticoagulated whole blood.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0469-2015·2014-12-03

    Novadaq LUNA Chest Recalled for Sterile Labeling Error

    Novadaq Technologies is recalling 828 LUNA Chest units because non-sterile drapes were inadvertently mislabeled as sterile.

    Product
    LUNA Chest, Model No. LU4006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0257-2015·2014-12-03

    Zydus Recalls Amlodipine Besylate Tablets Due to Discoloration

    Zydus Pharmaceuticals is recalling Amlodipine Besylate 10 mg tablets due to brown spots embedded in the product.

    Product
    AMLODIPINE BESYLATE — AMLODIPINE BESYLATE (AMLODIPINE BESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0463-2015·2014-12-03

    Abbott m2000sp Software Incompatibility Recall for Nucleic Acid Testing

    Abbott Molecular is recalling m2000sp CD-ROMs because some Application Specifications are incompatible with software versions 6.0 and 7.0, causing error code 9000.

    Product
    Abbott m2000sp, an automated system for performing sample preparation for nucleic acid testing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0470-2015·2014-12-03

    Novadaq Non-Sterile Drape Recalled for Incorrect Sterile Labeling

    Novadaq Technologies is recalling 324 non-sterile LUNA drapes that were inadvertently mislabeled with an additional contents sterile label.

    Product
    Non-sterile drape
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15710·2014-12-02

    Eaton Recalls Electrical Meter Breakers Due to Shock Hazard

    Eaton is recalling about 1,100 MBED 3042 series residential meter breakers because their electrical components can be easily accessed, posing a shock hazard.

    Product
    Electrical Meter Breakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15039·2014-12-02

    Daikin Streamer Air Purifiers Recalled for Fire Hazard

    Daikin is recalling Streamer air purifiers because the circuit board can overheat and cause a fire. No injuries have been reported.

    Product
    Daikin Streamer air purifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V763000·2014-12-01

    Subaru Recalls 2003-2005 Models for Air Bag Inflator Rupture Risk

    Subaru is recalling 2003-2005 Legacy, Outback, and Baja vehicles in high-humidity areas because the passenger air bag inflator may rupture during deployment.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY, BAJA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V764000·2014-12-01

    Mercedes-Benz Recalls 2014-2015 Sprinter Vehicles Due to Oil Leak Fire Risk

    Mercedes-Benz is recalling 2014-2015 Sprinter 2500 and 3500 vans because oil may leak from the chain tensioner gasket, posing a fire and road hazard risk.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V762000·2014-12-01

    Mercedes-Benz Recalls 2014-2015 Models Due to Oil Leak Fire Risk

    Mercedes-Benz is recalling 4,871 vehicles because oil may leak from the chain tensioner gasket, posing a fire and road hazard risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLK250, ML250, E250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V683000·2014-11-28

    Nissan and Infiniti Recall Vehicles for Fuel Pressure Sensor Defect

    Nissan is recalling specific 2012-2015 Nissan Juke and Infiniti models because loose fuel pressure sensors may cause fuel leaks and potential fires.

    Product
    INFINITI — INFINITI, NISSAN QX56, JUKE, M56, QX80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V759000·2014-11-28

    Thomas Built Buses Minotour Recalled for Loose Fuel Tank Strap

    Daimler Trucks North America is recalling 2013-2015 Thomas Built Buses Minotour non-school buses because a loose fuel tank strap may allow the tank to contact the ground, increasing the risk of a fuel leak and fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide