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.

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.

56751–56775 of 74005

  • SevereNHTSA·14V652000·2014-10-17

    Keystone Recalls 2014-2015 Dutchmen Travel Trailers Due to Electrical Fire Risk

    Keystone RV Company is recalling 2014-2015 Dutchmen Aerolite and Denali travel trailers because a 12V breaker may not be connected to the protected terminal, posing a fire risk.

    Product
    DUTCHMEN — DUTCHMEN, KEYSTONE AEROLITE, DUTCHMEN DENALI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V649000·2014-10-17

    Ford Recalls 2015 Mustangs for Passenger Air Bag Sensor Defect

    Ford is recalling 2015 Mustangs because the passenger seat sensor may misclassify occupant size, potentially causing improper air bag deployment in a crash.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V651000·2014-10-17

    Turtle Top Transit Buses Recalled for Wheelchair Lift Platform Cracking Risk

    Turtle Top is recalling specific transit buses equipped with Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk to operators.

    Product
    TURTLE TOP — TURTLE TOP VANTERRA, ODYSSEY XL, ODYSSEY LT, ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15706·2014-10-16

    Honda Recalls 2014 Pioneer 700 Off-Highway Vehicles Due to Fire Hazard

    American Honda is recalling about 15,400 2014 Honda Pioneer 700 recreational off-highway vehicles because debris on the skid plate can ignite from the exhaust system.

    Product
    Recreational off-highway vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15707·2014-10-16

    Briggs & Stratton Recalls Snapper Riding Mowers Due to Brake Failure Risk

    Briggs & Stratton is recalling about 8,500 Snapper rear engine riding mowers because a weld on the drive axle can fail, causing loss of brake control.

    Product
    Brigg & Stratton Snapper Rear Engine Riding Mower
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V648000·2014-10-16

    BMW Recalls 2015 X3 and X4 Vehicles for Rearview Mirror Defect

    BMW is recalling 2015 X3 and X4 vehicles because the driver's side exterior rearview mirror may not meet US safety standards, increasing crash risk.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15008·2014-10-16

    Sanus Simplicity SLF5 Wall Mounts Recalled Due to Impact Hazard

    Milestone AV Technologies is recalling Sanus Simplicity SLF5 wall mounts because a nut can loosen, causing the TV to detach and pose an impact hazard.

    Product
    Sanus Simplicity SLF5 flat screen television wall mounts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0006-2015·2014-10-15

    Expo Fresh Recalls Roma Tomatoes Due to Salmonella Risk

    Expo Fresh L.L.C is recalling 10,072 boxes of Roma Tomatoes due to potential Salmonella contamination. The product was distributed nationwide.

    Product
    Roma Tomatoes, 25lbs. case
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0019-2015·2014-10-15

    Mars Recalls Twix Unwrapped Bites for Undeclared Peanuts and Eggs

    Mars Chocolate North America is recalling Twix Unwrapped Bites due to undeclared peanuts and eggs. The recall covers 13,560 pouches distributed nationwide.

    Product
    Twix Unwrapped Bites 7.0 oz. distributed by Mars chocolate na, llc Hackettstown, NJ 07840-1503 USA UPC 040000484325 contained in a Metallized-golden stand up pouch (SUP) package 5 pouches per carton, 2 cartons per case
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0011-2015·2014-10-15

    Unique Pharmaceutical Recalls N-Acetyl Cysteine Vials Due to Non-Sterility

    Unique Pharmaceutical, Ltd is recalling one lot of N-Acetyl Cysteine 20% vials because testing revealed the presence of Herbaspirillum huttiense bacteria.

    Product
    N-Acetyl Cysteine 20% 4 mL Vial Stock Code: 4133
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V647000·2014-10-15

    Lexus Fuel Leak Recall for 2006-2011 Models

    Toyota is recalling 2006-2011 Lexus vehicles because fuel may leak from the pressure sensor, increasing fire risk.

    Product
    LEXUS — LEXUS LS460, LS460L, IS F, IS 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0017-2015·2014-10-15

    Richard-Allan Scientific Recalls Specimen Transportation System Due to Concentration Issues

    Richard-Allan Scientific is recalling 264 cases of its Specimen Transportation System because the NBF concentration may be outside specifications.

    Product
    Richard-Allan Scientific Specimen Transportation System. 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0007-2015·2014-10-15

    Frozen Jalapeno Bagels Recalled Due to Glass and Stone Contamination

    Wholesome Harvest Baking is recalling frozen jalapeno bagels because of reports of glass pieces and stones in the product.

    Product
    Frozen jalapeno bagels sold under the Maple Leaf Bakery brand in three different sizes: 3 oz. (64 bagels/case), 4 oz. (78 bagels/case), and 4.5 oz. (72 bagels/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0013-2015·2014-10-15

    Richard-Allan Scientific Recalls Specimen Transportation System Due to Concentration Issues

    Richard-Allan Scientific is recalling 285 cases of its Specimen Transportation System because the NBF concentrations may not meet specifications.

    Product
    Richard-Allan Scientific Specimen Transportation System. Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0015-2015·2014-10-15

    Richard-Allan Scientific Recalls Bio-Tite Specimen Containers Due to Concentration Issues

    Richard-Allan Scientific is recalling Bio-Tite Specimen Containers because the NBF concentration may be outside specifications.

    Product
    Richard-Allan Scientific Bio-Tite Specimen Containers. Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0016-2015·2014-10-15

    Richard-Allan Scientific Recalls 10% Neutral Buffered Formalin Due to Concentration Issues

    Richard-Allan Scientific is recalling 199 cases of 10% Neutral Buffered Formalin because the chemical concentration may be outside of desired specifications.

    Product
    Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0018-2015·2014-10-15

    Cardinal Health Prefilled Buffered 10% Formalin Recalled for Concentration Issues

    Richard-Allan Scientific Company is recalling Cardinal Health Prefilled Buffered 10% Formalin because the formalin concentration may be outside specifications.

    Product
    Cardinal Health Prefilled Buffered 10% Formalin. Product Usage:10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0006-2015·2014-10-15

    Janssen Recalls Xarelto Tablets Due to Microbial Contamination

    Janssen Ortho L.L.C. is recalling 13,500 bottles of Xarelto (rivaroxaban) 15 mg tablets due to confirmed microbial contamination in a sales sample.

    Product
    Xarelto (rivaroxaban) Tablets 15 mg per tablet, 5 count bottle, Rx Only, Manufactured by: JOLLC, Gurabo, PR 00778 NDC 50458-578-99
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0012-2015·2014-10-15

    Richard-Allan Scientific Recalls Protocol 10% NBF Tissue Fixative

    Richard-Allan Scientific is recalling 175 cases of Protocol 10% NBF tissue fixative because the concentration may be outside specifications.

    Product
    Protocol 10% NBF Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0058-2015·2014-10-15

    Biomet Recalls Mamba Disposable Nitinol Needles Due to Breakage Risk

    Biomet is recalling 164 Mamba Disposable Nitinol Needles because high friction may cause the needles to break during use.

    Product
    Mamba Disposable Nitinol Needle. The Biomet Sports Medicine Mamba instruments are utilized to aid in passing suture through soft tissue. The Mamba Needle is designed for use with the Mamba Suture Passer. The needles are sterile, disposable, and for single-patient use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0007-2015·2014-10-15

    Zydus Recalls Atenolol Tablets Due to Superpotent Drug Complaint

    Zydus Pharmaceuticals is recalling 5,400 bottles of Atenolol 25 mg tablets nationwide after a pharmacist reported that several tablets appeared noticeably thicker.

    Product
    ATENOLOL — ATENOLOL (ATENOLOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0009-2015·2014-10-15

    Mylan Recalls Metoprolol Succinate Tablets Due to Foreign Object Presence

    Mylan Pharmaceuticals is recalling 15,966 bottles of Metoprolol Succinate Extended-release Tablets 50mg because a pharmacist reported finding a rogue tablet of different size and markings in a bottle.

    Product
    Metoprolol Succinate Extended-release Tablets, USP 50mg, 90-count Bottles, Rx only, Mfg by Mylan Pharmaceuticals, Inc. Morgantown, WV 26505. NDC 0378-4596-77.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0014-2015·2014-10-15

    Richard-Allan Scientific Recalls 10% Neutral Buffered Formalin Due to Concentration Issues

    Richard-Allan Scientific is recalling 10% Neutral Buffered Formalin because the concentration may be outside specifications. The product is used to fixate tissue for histological examination.

    Product
    Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0052-2015·2014-10-15

    Zoll Pro-padz Sterile Electrodes Recalled Due to Sterility Concerns

    Bio-Detek is recalling 237 cases of Zoll Pro-padz Sterile Multi-Function Electrodes because product sterility is not assured. The affected lots were distributed worldwide.

    Product
    ZOLL Pro-padz Sterile Multi-Function Electrodes (MFE) Part Number: 8900-4012 Product Usage: These MFE Electrodes are used in connection with ZOLL Defibrillators for Adult patients. These disposable single use MFEs are processed through Gamma Radiation to a SAL of 10-6 per…
    Category
    Medical Device
    Distribution
    Distributed nationwide