The Recall Desk

State

US Virgin Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43626–43650 of 73984

  • LowFDA (Devices)·Z-1892-2017·2017-05-10

    Zimmer TM Ardis Interbody System Recalled for Procedural Error in Literature Approval

    Zimmer Trabecular Metal Technology, Inc. is recalling the TM Ardis Interbody System due to a procedural error in the approval of literature, resulting in the unauthorized release of certain content.

    Product
    The TM Ardis Interbody System implant is a convex, straight TLIF or PLIF device for interbody fusion of the anterior column of the spine. TM Ardis is designed for fusing the adjacent bony surfaces and may be used to replace a disc at one or two contiguous levels in L2-S1. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0692-2017·2017-05-10

    Aripiprazole Tablets Recalled for Out-of-Specification Assay Results

    The Harvard Drug Group is recalling Aripiprazole Tablets, 2 mg, due to out-of-specification assay results. The recall covers 36,990 tablets distributed nationwide and in Puerto Rico.

    Product
    Aripiprazole Tablets, 2 mg, 30 count unit dose box, Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada, Distributed by Major Pharmaceuticals, Livonia, MI NDC 0904-6509-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1949-2017·2017-05-10

    Anspach Effort Recalls Electronic Foot Controls Due to Missing Service Interval

    The Anspach Effort, Inc. is recalling 821 Electronic Foot Controls because the supplied directions for use did not contain a recommended service interval.

    Product
    Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1936-2017·2017-05-10

    Anspach Effort AL-III-DISS Adapter Recall for Missing Service Interval

    The Anspach Effort, Inc. is recalling five AL-III-DISS Adapters because the supplied directions for use did not contain a recommended service interval.

    Product
    AL-III-DISS Adapter Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1956-2017·2017-05-10

    Anspach Effort Recalls System Consoles for Missing Service Interval Instructions

    The Anspach Effort, Inc. is recalling 462 System Console units because the supplied directions for use did not contain a recommended service interval.

    Product
    System Console, Single Port, with irrigation Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V302000·2017-05-09

    FCA Recalls Ram Trucks Due to Disabled Side Curtain Air Bags

    FCA US LLC is recalling 2013-2016 Ram 1500, 2500, and 3500 trucks because a sensor fault may disable side curtain air bags and seat belt pretensioners, increasing injury risk in crashes.

    Product
    RAM — RAM 1500, 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-050917·2017-05-09

    FSIS Public Health Alert for Frozen Pork and Chicken Due to Listeria

    The USDA FSIS issued a public health alert for frozen ready-to-eat fried chicken and pork sausage products due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert for Pork and Poultry Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17744·2017-05-09

    Honda Recalls 2017 Pioneer 700 Vehicles Due to Seat Belt Defect

    American Honda is recalling about 2,200 2017 Pioneer 700 recreational off-highway vehicles because a manufacturing defect may cause the front passenger seat belt buckle to fail.

    Product
    Recreational off-highway vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V306000·2017-05-08

    Forest River Recalls 2017 XLR ToyHaulers for Incorrect Tire Pressure Label

    Forest River is recalling 2017 XLR ToyHauler trailers because the Federal Placard incorrectly lists rear tire pressure as 50psi instead of 80psi, which could lead to tire failure.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide