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.

58751–58775 of 74011

  • HighFDA (Food)·F-1863-2014·2014-04-23

    Parkers Farm Fire Roasted Salsa Recalled for Listeria Risk

    Parkers Farm Inc is recalling Fire Roasted Salsa due to potential Listeria monocytogenes contamination. Consumers should check sell-by dates and stop using the product.

    Product
    Fire Roasted Salsa sold under the following sizes and brands: 1. Parkers Farm or Parkers label in 16 ounce (51605) container with snap on lid, 1 gallon (11900) jug with screw on lid; 2. San Pablo in 1 gallon jug with screw on lid (12827).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·14V216000·2014-04-23

    Ford E-350 wheelchair lift roll stop latch recall

    Advanced Wheels is recalling 2008-2010 Ford E-350 vans with wheelchair lifts due to bent or misaligned roll stop latches that could allow occupants to fall.

    Product
    FORD — FORD E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1466-2014·2014-04-23

    Edwards Lifesciences Recalls Fem-Flex II Arterial Cannulae Due to Tip Separation

    Edwards Lifesciences is recalling 13,115 Fem-Flex II Arterial and femoral Cannulae because the dilator tips may separate. The recall covers units distributed nationwide and to foreign, government, and military consignees.

    Product
    Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae, arterial cannula sizes 16, 18 and 20 French, models: FEMII016A, FEMII016AS, FEMII018A, FEMII018AS, FEMII020A, and FEMII020AS.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1862-2014·2014-04-23

    Parkers Farm Hot Salsa Recalled for Potential Listeria Contamination

    Parkers Farm Inc is recalling Hot Salsa due to potential Listeria monocytogenes contamination. Consumers should check sell-by dates and discard affected products.

    Product
    Hot Salsa sold under the following sizes and brands: 1. Parkers Farm or Parkers label in 16 ounce (51205) container with snap on lid, 32 ounce (10894) jug with screw on lid;
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·14V198000·2014-04-23

    Autocar Recalls 2012-2014 Xpert Vehicles for Seat Mounting Defect

    Autocar is recalling 2012-2014 Xpert vehicles because floor mats may have prevented proper seat bolt tightening, increasing injury risk in crashes.

    Product
    AUTOCAR — AUTOCAR XPERT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1865-2014·2014-04-23

    Parkers Farm Black Bean Salsa Recalled for Listeria Risk

    Parkers Farm Inc is recalling Black Bean & roasted Chili Salsa due to potential Listeria monocytogenes contamination.

    Product
    Black Bean & roasted Chili Salsa sold under the following sizes and brands: 1. Parkers Farm or Parkers label in 32 ounce (80598) jug with screw on lid;
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1464-2014·2014-04-23

    Philips Ingenuity Core 128 CT Systems Recalled for Software Reconstruction Failures

    Philips is recalling 116 Ingenuity Core 128 CT systems worldwide because a software upgrade caused intermittent reconstruction failures.

    Product
    Ingenuity Core 128, Computed Tomography X-ray systems, Philips Medical Systems (Cleveland), Inc.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1456-2014·2014-04-23

    Synthes CMF Battery Powered Driver Recalled for Misleading Case Graphics

    Synthes is recalling CMF Battery Powered Drivers because the packaging graphics suggest off-label use with taps, which is not intended.

    Product
    Synthes CMF Battery Powered Driver, Part no. 305.840. Used to place screws in the cranialfacial bones, and to drill and/or tap holes to prepare cranialfacial bones for screw insertion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1821-2014·2014-04-23

    Vitamin E Softgels Recalled for Labeling Discrepancy

    Magno Humphries Laboratories is recalling Vitamin E softgels because the main label states 1000 IU while the Supplement Facts panel indicates 200 IU.

    Product
    OPTIMUM E-1000 IU Gluten Free Dietary Supplement 100 SOFTGELS Product is packaged in a white HDPE bottle with foil cap under the white plastic cap. Bottle contains 100 softgel caps. UPC 0 43292 56291 7.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1468-2014·2014-04-23

    Codman Certas Programmable Valves Recalled for Missing Verification Tools

    Codman & Shurtleff is recalling 9,445 units of Certas Programmable Valves to ensure customers have tools to verify valve settings and location on x-ray images.

    Product
    CODMAN CERTAS Programmable Valves, central nervous system shunt, models as follows: 82-8800 In Line Valve Only 82-8801 In Line Valve with Catheter and Accessories 82-8802 In Line Valve with Unitized Catheter and Accessories 82-8803 In line Valve with Unitized BACTISEAL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1457-2014·2014-04-23

    Synthes Hohmann Retractor Recalled for Incorrect Part Number Etching

    Synthes, Inc. is recalling 20 Hohmann retractors because they were mis-etched with the wrong part number.

    Product
    The Synthes Hohmann Retractor, 43 mm Long Shank, Angled 235 mm Product Usage: Used to expose bone for procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·14151·2014-04-22

    Troy-Bilt Electric Leaf Blowers Recalled Due to Laceration Hazard

    MTD is recalling Troy-Bilt electric leaf blowers because the impeller can break and strike the operator, posing a laceration hazard.

    Product
    Troy-Bilt electric leaf blowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14154·2014-04-22

    Excalibur Recalls Matrix Mega 405 Crossbows Due to Injury Hazard

    Excalibur is recalling about 1,000 Matrix Mega 405 crossbows because they can fire unexpectedly without the trigger being pulled, posing an injury risk.

    Product
    Excalibur Matrix Mega 405 Crossbows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14153·2014-04-22

    E-Z-GO Recalls Golf and Utility Vehicles Due to Steering Nut Hazard

    E-Z-GO is recalling approximately 30,000 golf, shuttle, and off-road utility vehicles because an insufficiently tightened steering wheel nut may reduce steering control.

    Product
    Golf cars, shuttles and off-road utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V214000·2014-04-22

    Grand Design Solitude Fifth Wheel Travel Trailer Microwave Recall

    Grand Design is recalling 2014 Solitude fifth wheel travel trailers equipped with certain Frigidaire microwaves that may start on their own and cause a fire.

    Product
    GRAND DESIGN — GRAND DESIGN SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E018000·2014-04-21

    Gillig Recalls Aftermarket Accelerator Pedals Due to Spring Failure Risk

    Gillig LLC is recalling 98 aftermarket accelerator pedals where mechanical springs may break, preventing the pedal from returning to idle and increasing crash risk.

    Product
    VEHICLE SPEED CONTROL:ACCELERATOR PEDAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·024-2014·2014-04-20

    Oscar Mayer Classic Wieners Recalled for Undeclared Milk Allergen

    Kraft Foods Group is recalling approximately 96,000 pounds of Oscar Mayer Classic Wieners because the packages may contain cheese dogs with undeclared milk.

    Product
    Kraft Heinz Foods Company — Missouri Firm Recalls Hot Dog Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·023-2014·2014-04-19

    Gold Creek Foods Recalls Chicken Breast Tenders Due to Undeclared Allergens

    Gold Creek Foods is recalling approximately 24,000 pounds of fully cooked breaded chicken breast products because they contain undeclared egg and wheat allergens.

    Product
    Gold Creek Foods LLC — Georgia Firm Recalls Chicken Breast Tenders Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V211000·2014-04-18

    BMW Recalls 2013 R 1200 GS Motorcycles for Transmission Seal Defect

    BMW is recalling 2013 R 1200 GS motorcycles because transmission pressure may push the output seal out of place, causing oil to leak onto the rear tire and increasing crash risk.

    Product
    BMW — BMW R 1200 GS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V207000·2014-04-18

    Mack Pinnacle Trucks Recalled for Missing Brake Air Tank Valve

    Mack is recalling 2014-2015 Pinnacle trucks because a missing pressure relief valve could cause the air tank to rupture, increasing injury risk.

    Product
    MACK — MACK PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14T004000·2014-04-18

    Federal Couragia A/T Tires Recalled for Steel Belt Separation

    Federal Corporation is recalling specific Couragia A/T tires due to steel belt separation that can cause shoulder cracks and loss of pressure.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14T002000·2014-04-18

    Alliance Tires Recalled for Missing Sidewall Markings

    Alliance Tire Americas is recalling specific 14-17.5 ML Alliance 239 tires because they lack required sidewall markings, which could lead to overloading and blowouts.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V206000·2014-04-18

    Prevost Recalls Coaches Due to Seat Belt Damage Risk

    Prevost is recalling 80 X3-45 and H3-45 coaches because raised wheelchair seats may damage seat belts, increasing injury risk in a crash.

    Product
    PREVOST — PREVOST X3-45, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V205000·2014-04-18

    Mack Trucks Recalls CXU Models Due to Blocked Rear Reflectors

    Mack Trucks is recalling 2010-2015 CXU trucks because exhaust pipes may block rear reflectors, reducing visibility and increasing crash risk.

    Product
    MACK — MACK PINNACLE (CXU), CXU
    Category
    Vehicle
    Distribution
    Distributed nationwide