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.

58026–58050 of 74005

  • ModerateFDA (Devices)·Z-1856-2014·2014-07-02

    NxStage Dialysate Sacks Recalled for Excess Aluminum Levels

    NxStage Medical is recalling dialysate sacks used with the PureFlow SL system because they contain aluminum levels exceeding internal specifications.

    Product
    NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-303 Lactate 45, Potassium 1, Sodium 140, Calcium 3, Magnesium 100m Chloride 100m, Glucose (mg/dL) 100 Batch Size (liters) 50 The SAK is one of the disposables used with NxStage PureFlow SL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1411-2014·2014-07-02

    Bausch & Lomb Recalls Sodium Chloride Ophthalmic Ointment Due to Crystallization

    Bausch & Lomb is recalling 35,253 tubes of Sodium Chloride Hypertonicity Ophthalmic Ointment, 5%, due to crystal precipitate formation causing a gritty sensation in the eye.

    Product
    Sodium Chloride Hypertonicity Ophthalmic Ointment, 5%, 1/8 oz. (3.5 g) tube per carton, Distributed by Major Pharmaceuticals, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0904-5315-38, UPC 3 09045 31538 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1860-2014·2014-07-02

    NxStage Dialysate Sacks Recalled for Excess Aluminum Levels

    NxStage Medical is recalling dialysate sacks used in home dialysis systems because aluminum levels exceeded internal specifications.

    Product
    NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-307 Lactate 40, Potassium 1, Sodium 140, Calcium 3, Magnesium 1, Chloride 105, Glucose (mg/dL) 100 Batch Size (liters) 50 The SAK is one of the disposables used with NxStage PureFlow SL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1842-2014·2014-07-02

    Zimmer Recalls VerSys Hip Stems Due to Material Inspection Failures

    Zimmer, Inc. is recalling 147 VerSys Hip System stems because supplier forgings failed routine material inspections.

    Product
    VerSys¿ Hip System, Beaded Fullcoat Stems, Zimmer, Inc., Warsaw, IN 46581
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1928-2014·2014-07-02

    Alere Triage BNP Calibrators Recalled Due to Mislabeling

    Alere San Diego is recalling BNP calibrators because a Level 5 bottle contains Level 4 material, causing calibration failures.

    Product
    Alere Triage BNP Calibrators for the Beckman Coulter Access Family of Immunoassay Systems, Model No. 98202 The Alere Triage BNP test is intended for use with the Beckman Coulter Access Family of Immunoassay Systems for the In Vitro quantitative measurement of B-type…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1865-2014·2014-07-02

    Philips Recalls Ingenia MRI Systems Due to Incorrect Nut Material

    Philips is recalling 24 Ingenia 1.5T MRI systems because some units shipped between December 2013 and March 2014 were supplied with incorrect M10 nuts instead of A4 stainless steel nuts.

    Product
    Ingenia 1.5T, magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1863-2014·2014-07-02

    Philips Recalls Ingenia 1.5T MRI Systems Due to Incorrect Hardware

    Philips Medical Systems is recalling 33 Ingenia 1.5T MRI systems because incorrect M10 nuts were installed on the rear cover set.

    Product
    Ingenia 1.5T R5, magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1930-2014·2014-07-02

    Microgenics Recalls MAS Omni Immune PRO Controls Due to Labeling Error

    Microgenics Corporation is recalling MAS Omni Immune PRO Controls because the package insert failed to reflect the removal of the constituent Inhibin A.

    Product
    MAS Omni Immune PRO Controls
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1929-2014·2014-07-02

    Microgenics Recalls MAS Omni Immune Controls Due to Labeling Error

    Microgenics Corporation is recalling MAS Omni Immune Controls because the package insert failed to reflect the removal of the constituent Inhibin A.

    Product
    MAS Omni Immune Controls
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V396000·2014-07-01

    Volkswagen Recalls 2009 Routans for Ignition Switch Safety Defect

    Volkswagen is recalling 2009 Routans because the ignition switch may move out of the run position, turning off the engine and disabling safety systems.

    Product
    VOLKSWAGEN — VOLKSWAGEN ROUTAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V386000·2014-07-01

    Mercedes-Benz Recalls 2014 SL and SLK Models for Air Bag Defect

    Mercedes-Benz is recalling 2014 SL and SLK models because the front passenger air bag may not deploy properly, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SL550, SLK55, SL63, SLK250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V395000·2014-07-01

    Land Rover Recalls LR2 and Range Rover Evoque for Air Bag Defect

    Land Rover is recalling 2010-2015 LR2 and 2012-2013 Range Rover Evoque vehicles because a component failure may disable the front passenger air bag, increasing injury risk in a crash.

    Product
    LAND ROVER — LAND ROVER LR2, RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14C004000·2014-06-30

    Graco Recalls Rear-Facing Child Restraints Due to Stuck Harness Buckle

    Graco is recalling specific rear-facing child seats because the harness buckle may get stuck, making it difficult to remove a child in an emergency.

    Product
    CHILD SEAT:HARNESS/CROTCH BUCKLE recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V380000·2014-06-30

    Nova Bus Recalls LFS Transit Buses Due to ABS Warning Light Defect

    Nova Bus is recalling 796 LFS transit buses from model years 2004 and 2006-2013 because the ABS malfunction light may not illuminate if the control unit loses power.

    Product
    NOVA BUS — NOVA BUS LFS, NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V374000·2014-06-27

    GM Recalls 2014-2015 Trucks and SUVs for Transfer Case Defect

    General Motors is recalling specific 2014-2015 Chevrolet and GMC vehicles because an electrical short may cause the transfer case to shift to neutral unexpectedly.

    Product
    GMC — GMC, CHEVROLET YUKON, SILVERADO, TAHOE, SIERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide