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.

55576–55600 of 74005

  • HighNHTSA·15V045000·2015-01-28

    Honda Recalls 2003-2004 Odyssey and 2003 Acura MDX for Air Bag Defect

    Honda is recalling 2003-2004 Odyssey and 2003 Acura MDX vehicles because electrical noise may cause air bags to deploy unexpectedly, increasing injury risk.

    Product
    HONDA — HONDA, ACURA ODYSSEY, MDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0993-2015·2015-01-28

    Maquet Tegris System Recalled Due to Software Error in Operating Table Commands

    Maquet Medical Systems USA is recalling six units of the Tegris System because a software error switches leg movement commands for the Magnus OR table.

    Product
    TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Tegris OR Integration System is designed to be used as the central operating unit in an operating room. The integration system has two main functions: Recording and distribution of images and videos and interaction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V040000·2015-01-28

    Ford Recalls Taurus and Lincoln MKS for Door Handle Spring Defect

    Ford is recalling 2010-2013 Taurus and 2011-2013 Lincoln MKS vehicles because an interior door handle spring may unseat, preventing the handle from returning to its stowed position.

    Product
    FORD — FORD, LINCOLN TAURUS, MKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1000-2015·2015-01-28

    BD Biosciences Recalls Contaminated CD8 PE In Vitro Diagnostic Reagent

    BD Biosciences is recalling one lot of CD8 PE reagent contaminated with CD4 FITC, which may cause incorrect patient data.

    Product
    CD8 (Leu-2a) PE (In vitro diagnostic), Catalog number 340046. Hematology: Single color direct immunofluorescence reagent for enumerating percentages of mature human suppressor/cytotoxic (CD8+) lymphocytes in erythrocyte-lysed whole blood or peripheral blood mononuclear cell…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0998-2015·2015-01-28

    Cordis POWERFLEX PRO PTA Dilatation Catheter Recall for Unsterilized Unit

    Cordis Corporation is recalling one unsterilized unit of the POWERFLEX PRO PTA Dilatation Catheter from a demonstration lot left at a hospital.

    Product
    Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, infra popliteal and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. The device is also…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1002-2015·2015-01-28

    BD Biosciences Recalls Contaminated Anti-Lambda APC-H7 Antibody Lots

    BD Biosciences is recalling two lots of Anti-Lambda APC-H7 antibody due to contamination with CD38 antibody. The product is used for in vitro flow cytometric immunophenotyping.

    Product
    Anti-Lambda APC-H7, Catalog Number 656157. Product Usage: Intended for in vitro flow cytometric immunophenotyping of hematologic disorders.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0378-2015·2015-01-28

    Mylan Lamotrigine Tablets Recalled for CGMP Deviations

    Mylan Institutional is recalling 3,993 cartons of Lamotrigine 200 mg tablets because they were not manufactured according to Good Manufacturing Practices.

    Product
    LAMOTRIGINE TABLETS, 200 mg, 100 Tablets (10 tablets per blister card x 10 blister cards per carton), Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 51079-866-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1001-2015·2015-01-28

    Genetic Testing Institute Recalls PF4 Concentrated Wash Reagent Lots

    Genetic Testing Institute is recalling specific lots of PF4 Concentrated Wash (10x) because the reagent is slightly more dilute than intended, which may cause false positive test results.

    Product
    PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG (catalog numbers HAT13G, HAT45G) and 2. ImmucorGamma LIFECODES PF4 Enhanced (catalog numbers X-HAT13, X-HAT45) The PF4 IgG assay is an Enzyme Linked…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1006-2015·2015-01-28

    Aptalis Flutter Percussor Respiratory Device Recalled for Packaging Defect

    Aptalis Pharmatech Inc. is recalling approximately 49,000 Flutter Percussor respiratory devices because the packaging may be difficult to open or close.

    Product
    FLUTTER Percussor respiratory device, packaged one unit per clear plastic package. Product Usage: Product is a percussor device, intended to be used as a mucus clearance device for patients with mucus producing respiratory conditions such as: atelectasis, bronchitis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0376-2015·2015-01-28

    3M ESPE Clinpro 5000 Toothpaste Recalled for Missing Lot and Expiration Dates

    3M ESPE is recalling 19,728 tubes of Clinpro 5000 Anti-Cavity Toothpaste because the primary boxes are missing lot numbers and expiration dates.

    Product
    3M ESPE Clinpro 5000 (1.1% Sodium Flouride), Anti-Cavity Toothpaste, 4 oz tube (NDC 48878-3130-04), Rx Only, Manufactured for 3M ESPE Dental Products, St. Paul, MN 55144
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V039000·2015-01-27

    Land Rover Recalls Range Rovers Due to Brake Hose Rupture Risk

    Jaguar Land Rover is recalling 2006-2012 Range Rovers because front brake hoses may rupture, causing loss of brake fluid and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V038000·2015-01-27

    Jaguar Recalls 2012-2015 XK Models for Front Side Lamp Defect

    Jaguar is recalling 2012-2015 XK vehicles because front side lamps may turn off after five minutes, reducing visibility and increasing crash risk.

    Product
    JAGUAR — JAGUAR XK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V036000·2015-01-27

    Peterbilt 389 Recall for Electronic Stability Control Sensor Defect

    PACCAR is recalling 2015 Peterbilt 389 trucks because an incorrect horn contact plate may damage the ESC steering angle sensor, increasing crash risk.

    Product
    PETERBILT — PETERBILT 389
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15064·2015-01-27

    Mirka Recalls Compact Electric Random Orbital Sanders Due to Fire Hazard

    Mirka Abrasives is recalling specific 5-inch and 6-inch compact electric random orbital sanders because they can short circuit, posing a fire hazard. No injuries or property damage have been reported.

    Product
    Random orbital sanders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V037000·2015-01-27

    Jaguar Recalls 2015 XJ Models for Incorrect Air Bag Manual Description

    Jaguar is recalling 1,346 model year 2015 XJ vehicles because the owner's manual incorrectly describes the Occupant Sensor System, potentially increasing injury risk in a crash.

    Product
    JAGUAR — JAGUAR XJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V035000·2015-01-27

    Crossroads Recalls 2015 Z1 Trailers Due to Incorrect Ramp Load Labels

    Crossroads RV is recalling 2015 Z1 toyhauler trailers because the front loading ramps display a 700-pound capacity limit, but the actual limit is 500 pounds.

    Product
    CROSSROADS — CROSSROADS Z1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·021-2015·2015-01-26

    Oscar's Hickory House Recalls Sausage for Undeclared Allergens

    Oscar's Hickory House is recalling approximately 376 pounds of sausage products due to misbranding and undeclared allergens, including soy, milk, wheat, and sulfites.

    Product
    Oscar's Hickory House Inc. — New York Firm Recalls Sausage Products Due to Misbranding and An Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V031000·2015-01-26

    GM Recalls 2015 Chevrolet Corvettes for Rear Suspension Defect

    General Motors is recalling 2015 Chevrolet Corvettes because a rear suspension part may not be tightened properly, which could separate and cause a crash.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V033000·2015-01-26

    Nissan and Infiniti Recall Vehicles Due to Hood Latch Defect

    Nissan is recalling specific 2013-2014 Pathfinder, JX35, and QX60 models because the hood latch may not engage fully, posing a crash risk if the hood opens while driving.

    Product
    INFINITI — INFINITI, NISSAN QX60 HYBRID, PATHFINDER HYBRID, PATHFINDER, JX35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V032000·2015-01-26

    Nissan Recalls Rogue Vehicles Due to Electrical Fire Risk

    Nissan is recalling 2008-2014 Rogue vehicles because an electrical short in the driver-side floor can cause a vehicle fire. Dealers will inspect and repair the wiring harness free of charge.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E004000·2015-01-26

    Cummins Recalls QSK50 Dual Fuel Engines Due to Fuel Leak Risk

    Cummins is recalling QSK50 Tier 2 Dual Fuel Engines used on oil well fracturing rigs because a cracked fuel inlet connection may cause a leak and increase fire risk.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·15V034000·2015-01-26

    MINI Cooper Recalled for Incorrect Tire Information Placard Weight Label

    BMW is recalling 2014-2015 MINI Cooper Hardtop vehicles because the Tire Information Placard lists an incorrect maximum capacity weight, failing to comply with federal safety standards.

    Product
    MINI — MINI COOPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V028000·2015-01-23

    Volkswagen Recalls 2014-2015 Models for Fuel Rail Leak Risk

    Volkswagen is recalling specific 2014-2015 Jetta, Passat, Golf, GTI, and Beetle models because a fuel rail sealing cap may fail, allowing fuel to leak into the engine compartment.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA, BEETLE, GTI, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15T002000·2015-01-23

    Goodyear Recalls Fortera HL Tires Due to Tread Cracking

    Goodyear is recalling specific Fortera HL tires due to tread cracking that could cause tire failure. Owners of affected 2015 GM vehicles or replacement tires should contact the manufacturer.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide