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.

60776–60800 of 74011

  • ModerateFDA (Devices)·Z-0393-2014·2013-12-04

    Synthes Material Mix Surgical Instruments Recalled Due to Material Error

    Synthes USA is recalling approximately 44 surgical instruments because a material batch was mixed with an incorrect material having lower hardness and corrosion resistance.

    Product
    Synthes Material Mix (Adjustable Cervical Distractor-Right, Matrix Distractor Rack, T-PAL Spacer Remover, Implant Inserter) Synthes Material Mix: Adjustable Cervical Distractor-Right is used to distract spine segment. Matrix Distractor Rack is used to distract the interbody…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0382-2014·2013-12-04

    Southern Implants Recalls Tri-Nex Healing Abutments Due to Labeling Error

    Southern Implants is recalling 197 Tri-Nex healing abutments because the packages were incorrectly labeled and contained the wrong product size.

    Product
    Tri-Nex Healing Abutment, 0.50 mm x 5 mm height, Catalog No. HA-L-50-5. The NSI Implant System is intended to be implanted in the upper and lower jaw arches to provide support for fixed or removable dental prostheses in a single tooth, partially edentulous prostheses, or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-022-2014·2013-12-04

    Novartis Recalls Loratadine Tablets Due to Chipped and Broken Pieces

    Novartis Consumer Health is recalling 11.8 million loratadine 10 mg antihistamine blister packs sold nationwide under seven different store brands because the tablets are chipped or broken.

    Product
    Loratadine, USP 10 mg, Antihistamine, packaged in blister packs. All manufactured by Novartis Consumer Health, Inc, Lincoln, NE / There are 7 different labels under which this product is packaged but the active ingredient is the same. 1) DOLLAR GENERAL LABEL: DG Health…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0383-2014·2013-12-04

    Thermo Fisher Recalls MAS Urinalysis Control Level 1 for Stability Failure

    Thermo Fisher Scientific is recalling 914 units of MAS Urinalysis Control Level 1 because the product failed to meet 30-day open vial stability specifications.

    Product
    MAS Urinalysis Control Level 1, Multi-analyte control (Assayed and Unassayed), Catalog/Part Numbers: 024222; Product is manufactured and distributed by Microgenics Corporation, a subsidiary of Thermo Fisher Scientific, Clinical Diagnostic Division, Fremont, CA MAS Urinalysis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0407-2014·2013-12-04

    Synthes Titanium Humeral Nail Recalled for Incorrect Packaging Labeling

    Synthes USA is recalling 14 Titanium Cannulated Humeral Nails because the packaging incorrectly depicts the device as having 3 distal holes instead of 2.

    Product
    Synthes Titanium Cannulated Humeral Nail Intended to aid in the alignment and stabilization of humeral fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0379-2014·2013-12-04

    Alere Cholestech LDX Lipid Profile-GLU Test Cassettes Recalled for Labeling Error

    Alere San Diego, Inc. is recalling 3,621 kits of Cholestech LDX Lipid Profile-GLU test cassettes because an incorrect lot number was printed on the packaging.

    Product
    Product Brand Name(s): Alere Cholestech LDX¿ Lipid Profile"GLU Test Cassette, Model 10-991. Product Generic Name: Alere Cholestech LDX¿ Lipid Profile"GLU Test Cassette. Description of the product: Lipid. Glucose panel Test cassettes. Product packaging: 10 individually pouched…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14036·2013-12-03

    L&F International Trade Recalls Renovated Mattresses for Fire Hazard

    L&F International Trade is recalling about 1,000 renovated mattresses and mattress sets because they fail to meet federal flammability standards, posing a fire hazard.

    Product
    Mattresses and mattresses with foundations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V605000·2013-11-29

    Daimler Recalls 2008-2009 Sterling Bullet Trucks for Tie Rod Fracture Risk

    Daimler Trucks North America is recalling 2,564 model year 2008-2009 Sterling Bullet trucks because the left outer tie rod ball stud may fracture, potentially causing loss of steering control.

    Product
    STERLING — STERLING BULLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13E065000·2013-11-29

    Airtex Recalls Fuel Pumps for Subaru Outback, Legacy, and Baja

    Airtex is recalling specific aftermarket fuel pumps for Subaru vehicles that may leak fuel when the tank is full, increasing fire risk.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY, BAJA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V597000·2013-11-29

    NABI Recalls 2013 Transit Buses Due to Wheel Lug Nut Loosening Risk

    North American Bus Industries is recalling 2013 31LFW and 40LFW transit buses because excessive paint on steel wheels may cause lug nuts to loosen, potentially leading to wheel detachment.

    Product
    NABI — NABI 40LFW, 31LFW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V606000·2013-11-29

    Thomas Built Buses Recall School Buses for Seat Belt Defect

    Daimler Trucks North America is recalling 2013-2015 Thomas Built school buses because seat belt buckles may fail to release, hindering emergency egress.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES, THOMAS BUILT SAF-T-LINER HDX, MINOTOUR, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V618000·2013-11-29

    Volvo Recalls 2014 Trucks Due to Seat Belt Buckle Defect

    Volvo is recalling 5,486 model year 2014 trucks because seat belt buckles may fail to release, hindering emergency egress.

    Product
    VOLVO — VOLVO VAH, VNM, VHD, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V601000·2013-11-29

    E-One Recalls 2013 Fire Fighting Vehicles for Seat Belt Defect

    E-One is recalling 2013 Quest, Cyclone II, and Typhoon fire fighting vehicles because seat belt buckles may fail to release, hindering emergency egress.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON, QUEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V619000·2013-11-29

    Mack Trucks Recalls 2014 CXU and MRU Models for Seat Belt Defect

    Mack Trucks is recalling 2014 CXU and MRU trucks because seat belt buckles may fail to release, potentially hindering emergency egress.

    Product
    MACK — MACK MRU, PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V604000·2013-11-29

    Daimler Trucks Recalls 2014 Freightliner and Western Star Models for Seat Belt Defect

    Daimler Trucks North America is recalling 26,310 model year 2014 Freightliner and Western Star trucks because seat belt buckles may fail to release properly, hindering emergency egress.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, 6900, CORONADO, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0261-2014·2013-11-27

    Medtronic Cougar Nitinol Guidewires Recalled for Coating Delamination Risk

    Medtronic Vascular is recalling specific Cougar Nitinol Workhorse Guidewires because the PTFE coating may delaminate and detach from the device.

    Product
    Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ, CGRXT190HS, CGRXT190J, CGRXT190S, CGRXT300HJ, CGRXT300HS, CGRXT300J, CGRXT300S Medtronic guide wires are steerable guide wires that are used for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0217-2014·2013-11-27

    Terri Lynn Deluxe Mixed Nuts Recalled for Undeclared Peanuts

    Terri Lynn Inc. is recalling Deluxe Mixed Nuts labeled 'No Peanuts' because the bags contain undeclared peanuts.

    Product
    Mixed nuts in a plastic bag labeled in part: PREMIUM QUALITY; Terri Lynn Inc.; Deluxe Mixed; No Peanuts; NET WT. 16 OZ. (1 LB.) 454 g; P.O. BOX 5118 ELGIN, IL 60121
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-001-2014·2013-11-27

    Teva Recalls Copaxone Syringes Due to Foreign Particulate Matter

    Teva Pharmaceuticals is recalling 6,803 cartons of Copaxone pre-filled syringes because a foreign particle was found in one unit.

    Product
    COPAXONE — COPAXONE (GLATIRAMER ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0268-2014·2013-11-27

    Medtronic Zinger Steerable Guidewires Recalled for Coating Delamination Risk

    Medtronic Vascular is recalling Zinger Steerable Guidewires because the PTFE coating may delaminate and detach from the device.

    Product
    ZINGER¿ Steerable Guidewire; Models: LVZRLS180J, LVZRLS180S, LVZRMS180J, LVZRMS180S, LVZRXT180J, LVZRXT180S Medtronic guide wires are steerable guide wires that are used for the introduction and placement of diagnostics or interventional devices in the coronary and peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide